Recent Progress in Materials is an international peer-reviewed Open Access journal published quarterly online by LIDSEN Publishing Inc. This periodical is devoted to publishing high-quality papers that describe the most significant and cutting-edge research in all areas of Materials. Its aim is to provide timely, authoritative introductions to current thinking, developments and research in carefully selected topics. Also, it aims to enhance the international exchange of scientific activities in materials science and technology.
Recent Progress in Materials publishes original high quality experimental and theoretical papers and reviews on basic and applied research in the field of materials science and engineering, with focus on synthesis, processing, constitution, and properties of all classes of materials. Particular emphasis is placed on microstructural design, phase relations, computational thermodynamics, and kinetics at the nano to macro scale. Contributions may also focus on progress in advanced characterization techniques.          

Main research areas include (but are not limited to):
Characterization & Evaluation of Materials
Metallic materials 
Inorganic nonmetallic materials 
Composite materials
Polymer Materials
Sustainable Materials and Technologies
Special types of Materials
Macro-, micro- and nano structure of materials
Environmental interactions, process modeling
Novel applications of materials

Archiving: full-text archived in CLOCKSS.

Free Publication in 2020
Current Issue: 2020  Archive: 2019
Open Access Review
The Use of Biomaterials in Internal Radiation Therapy

Ben Milborne 1, Abul Arafat 1, Rob Layfield 2, Alexander Thompson 3, Ifty Ahmed 1, *

  1. Advanced Materials Research Group, Faculty of Engineering, University of Nottingham, Nottingham NG7 2RD, United Kingdom
  2. School of Life Sciences, Faculty of Medicine and Health Sciences, University of Nottingham, Nottingham, NG7 2UH, United Kingdom
  3. University of Nottingham Biodiscovery Institute, Division of Cancer and Stem Cells, University of Nottingham, Nottingham, NG7 2UH, United Kingdom

Correspondence: Ifty Ahmed

Academic Editor: Hossein Hosseinkhani

Special Issue: Applications and Development of Biomaterials in Medicine

Received: March 18, 2020 | Accepted: May 06, 2020 | Published: May 12, 2020

Recent Progress in Materials 2020, Volume 2, Issue 2, doi:10.21926/rpm.2002012

Recommended citation: Milborne B, Arafat A, Layfield R, Thompson A, Ahmed I. The Use of Biomaterials in Internal Radiation Therapy. Recent Progress in Materials 2020;2(2):34; doi:10.21926/rpm.2002012.

© 2020 by the authors. This is an open access article distributed under the conditions of the Creative Commons by Attribution License, which permits unrestricted use, distribution, and reproduction in any medium or format, provided the original work is correctly cited.


Radiotherapy has become one of the most prominent and effective modalities for cancer treatment and care. Ionising radiation, delivered either from external or internal sources, can be targeted to cancerous cells causing damage to DNA that can induce apoptosis. External beam radiotherapy delivers either photon radiation (x-rays or gamma rays) or particle radiation (neutrons or protons) in a targeted manner to specific tumour locations. Internal radiotherapy involves placing radioactive sources within the body to deliver localised doses of therapeutic radiation to tumours using short range radionuclides. Biomaterials have been developed to allow more precise targeting of radiotherapy in order to reduce toxicity to surrounding healthy tissues and increase treatment efficacy. These unique biomaterials have been developed from polymers, glasses and ceramics. Polymeric materials have been used to both displace healthy tissue from tumours receiving radiation, and to deliver radioactive sources into the body. These polymers can respond to various stimuli, such as radiation or reactive oxygen species, to deliver therapeutic payloads to target tissue during or post radiotherapy. Glass-based biomaterials doped with radionuclides have also been developed to provide in situ radiotherapy. Novel biomaterials that can enhance the synergistic effect of other treatment modalities, such as chemotherapy and immunotherapy, continue to be developed. Theranostic materials that are capable of providing diagnostic information whilst simultaneously delivering a therapeutic effect to enhance radiotherapy are also briefly reviewed.

Graphical abstract

Click to view original image


Radiation therapy; biomaterials; cancer; brachytherapy; radiotherapy; radionuclides; glass; oncology

1. Introduction

Radiotherapy has become one of the most common and vital modalities for effective cancer treatment and care, and is used either alone or in combination with surgery, chemotherapy and immunotherapy in approximately half of all cancer cases worldwide [1]. Ionising radiation is utilised for the treatment of cancer due to its ability to deposit energy that damages the genetic material of cells, resulting in their inability to survive and proliferate further. The unregulated manner in which cancer cells rapidly proliferate means that they are more susceptible to radiation-induced DNA damage than normal healthy cells [2]. Irradiation can damage the DNA double helix structure by inducing DNA single and double-strand breaks, which in turn induces cellular events such as apoptosis, necrosis and abnormal mitosis [3]. DNA can also be damaged indirectly by reactive oxygen species (ROS) and through free radicals generated in cells by radiation (see Figure 1) [4]. The genomic instability of cancer cells means that they are inefficient or lack the ability to effectively repair DNA damage induced by radiation in comparison to normal cells. This mechanism underpins radiotherapy’s selectivity for inducing cancer cell death [5]. Unfortunately, radiation inadvertently causes damage to normal cells adjacent to cancerous cells, or those in the radiation path. As such, advancements in this field need to consider maximising the dose of radiotherapy to aberrant cancer cells whilst minimising exposure to normal healthy cells.

The dose of radiation can also directly influence the efficacy of treatment and in clinical settings the prescribed dose is usually a compromise between tumour control probability (TCP) and normal tissue complication probability (NTCP) [6]. The location of the tumour is the principal factor when considering NTCP and can vary throughout the body due to discrepancies in the radiosensitivity of different healthy and cancerous tissues. Since NTCP is the primary dose-limiting factor in radiotherapy multiple measures and techniques have been used to protect healthy tissue from radiation damage [7].

Depending on the type of cancer, radiotherapy can be used to cure localised cancer, either as palliative treatments to reduce symptoms, or to limit progression of the disease in incurable cases [8]. Radiotherapy is also often used in conjunction with other treatment modalities such as chemotherapy, immunotherapy and surgery. Radiotherapy can be delivered at different stages of a patient’s treatment regime. Neoadjuvant radiotherapy is performed pre-operatively with the aim of reducing the size of a tumour prior to surgical resection. Radiotherapy can also be used as an adjuvant therapy intra- operatively and post-operatively to help eliminate any residual tumour cells [9].

Click to view original image

Figure 1 (a) Schematic of how ionising radiation utilised for radiotherapy can damage DNA. Radiation can directly damage DNA or indirectly damage it through the generation of reactive oxygen species (ROS). (b) DNA damage can occur as a result of single-strand breaks (SSB), double-strand breaks (DSB) or other interactions with DNA and proteins.

The radiation itself can be delivered to cancerous targets in two opposing ways, Externally or Internally. External beam radiotherapy is the most prevalent form of radiotherapy used in the clinical setting and involves aiming high-energy rays, in the form of photons (X-rays or gamma rays), protons or particle radiation, from outside of the body to the specific tumour site. Conversely, internal radiotherapy occurs as a result of placing radioactive sources within the body, usually adjacent to or directly into the tumour itself [10]. Technological advances are continuing to drive progression in both external and internal radiotherapy in order to improve its therapeutic efficacy and reduce adverse effects.

Technological advances in imaging techniques in conjunction with the ability to shape radiation beams have resulted in the development of highly conformal external beam radiotherapies (EBRT). These techniques can accurately target a tumour site and deliver a maximum ionising radiation dose to the target whilst minimising the dose to surrounding healthy tissue [11]. Photon radiation, either x-rays produced by accelerating electrons or gamma rays from the decay of radioactive substances, are considered low linear energy transfer (LET) electromagnetic rays. Despite their low LET, the progression of linear electron accelerators which produce energy-tuneable bremsstrahlung x-rays has led to them being the most widespread source for many current EBRT regimens [12]. Particle radiation where heavier particles than electrons, in the form of neutrons or protons, are targeted to the tumour can also be performed. These particles have higher LET than photons and subsequent increased ability to damage cancer cells. The associated costs of generating the particles used and delivering particle radiation at treatment facilities has so far limited their use [13]. The modality, total dose and fraction of the radiotherapy schedule are considered on an individual basis and are dependent on both the condition of the patient and the location of the cancer [14].

There are several different types of photon beam radiotherapy used for cancer treatment. Three-dimensional conformal radiation therapy (3D-CRT) utilises computed tomography (CT) imaging to facilitate accurate determination of the tumour location and position of any potential adjacent critical structures. From this information, optimal beam placement from multiple directions can precisely match the shape of the tumour and therefore increase its irradiation whilst also identifying regions that necessitate shielding [15]. Intensity modulated radiation therapy (IMRT) is very similar to 3D-CRT with the advantage of being able to control the strength of the individual beamlets to certain regions. The intensity modulation ability of IMRT enables the delivery of irregular shaped radiation doses which can conform to the tumour whilst simultaneously avoiding critical structures [16]. Stereotactic body radiation therapy (SBRT) integrates these technological advances to precisely deliver very high individual doses of radiation over very few treatment fractions, to ablate well-defined small tumours. However, SBRT can subsequently damage adjacent tissue due to the elevated radiation dose [17].

Conformal external beam radiotherapies can allow for dose escalation to target regions whilst sparing normal tissue. This can lead to hypofractionated schedules, which involves the delivery of fewer, larger doses of radiotherapy in a highly precise manner which can provide radical curative effects at local tumour regions [18]. Despite this, clinical considerations such as location of the tumour and its subsequent proximity to surrounding critical organs and radiosensitive tissue can mean it may not always be possible to utilise EBRT. In such cases, internal radiotherapy becomes a viable option.

2. Internal Radiotherapy

Radiopharmaceuticals are medicinal products that contain radioisotopes which can be used for diagnostic or therapeutic clinical applications [19]. Radioisotopes such as 153Sa, 223Ra, 131I and 89Sr can be combined with an excipient for the systemic treatment of certain types of cancer including bone, prostate and thyroid cancer (see Table 1) [20]. Radiopharmaceuticals can be administered orally or intravenously with the aim of delivering them to accumulate at the desired cancer site. Conjugation of a radioisotope to monoclonal antibodies or to peptides that target cancer-associated cell surface antigens has also been explored in order to deliver a high dose of radiation to the tumour in therapeutic approaches known as radioimmunotherapy and peptide receptor radionuclide therapy [21,22].

Both 223Ra and 89Sr have been used for the treatment of secondary bone cancer, particularly when the cancer has metastasised to multiple bone sites, since they are both alkaline earth metals and follow very similar metabolic pathways in vivo to calcium [23]. As a result, these radiotherapeutic agents localise in bone mineral to act as bone-targeting therapies following intravenous injection. The uptake of these agents occurs preferentially at sites of active osteogenesis meaning that a greater concentration of these agents can occur at osteoblastic lesions and multiple metastatic sites simultaneously [24]. The ionising radiation emitted from these radiopharmaceuticals have varying tissue penetration depths and consequently are able to target bone metastases with minimal irradiation to adjacent soft tissues (see Table 1). The systemic administration of radiopharmaceuticals is limited to only a small number of aforementioned anatomical tumour locations. The majority of cancers require the ablative radiation dose to be targeted and to occur directly at the cancerous tissue over a short time period, with a rapid fall-off in dose to ensure minimal irradiation of healthy tissues [25].

Table 1 Common radiopharmaceuticals used in the systemic delivery of radionuclides.

3. Brachytherapy

Brachytherapy is a type of internal radiotherapy that involves the placement of sealed radioactive sources adjacent to or within the interstitium of cancerous tissue. The location in which the radioactive source is placed is used to classify the type of therapy i.e. intracavitary brachytherapy, interstitial brachytherapy, intraluminal/intravascular brachytherapy or superficial brachytherapy [29]. Brachytherapy can be further classified according to the dose rate applied, using the International Commission on Radiation Units stating that 0.4 to 2 Gy.h-1 is a low dose rate (LDR); 2 to 12 Gy.h-1 is a medium dose rate (MDR) and a high dose rate (HDR) is regarded as being greater than 12 Gy.h-1 [30]. In pulse dose rates, pulses of 1 to 3 Gy.h-1 are used to deliver a large number of small fractions with short intervals. HDR brachytherapy typically involves the temporary placement of a radioactive source, whilst LDR usually involves permanent implantation.

The location of the tumour and various patient related factors determine the type of brachytherapy conducted. For example, low-energy photon emitting sources, such as 125I and 103Pd, have typically been used for LDR whereas high energy emitting 192Ir and 60Co sources have been used for HDR [31]. In many instances, brachytherapy facilitates the delivery of a highly localised radiation dose that is unable to be achieved using conventional external beam radiation therapy [32]. This is because the absorbed dose is inversely proportional to the square of the distance of the radioactive source [33]. This means that as you double the distance from the radiation source, you reduce the dose by a factor of four as the energy is spread over four times the area. Prostate, cervical, oesophageal and certain types of breast cancer are the predominant types that have been used for treatment with brachytherapy [34].

Advanced imaging modalities, such as magnetic resonance imaging (MRI), computed tomography (CT) and ultrasound, have also been used in conjunction with sophisticated treatment planning software to determine the precise location in which to place the radioactive sources [35]. Correct placement of these sources enables the optimal dose distribution at the target site to be achieved on a patient specific basis. This allows for the delivery of conformal radiotherapy tailored to the size and shape of the individual tumour (see Figure 2) [25].

Click to view original image

Figure 2 Schematic of prostate brachytherapy delivery. Radioactive seeds are implanted into the prostate using trans-rectal ultrasound (TRUS) guiding and a grid template. TRUS is performed to identify the location of seeds deposited within the prostate and dosimetric plan is generated. Reproduced with permission from [36] (Cancer Research UK/ Wikimedia Commons).

Brachytherapy is an invasive technique as it requires surgical insertion to deliver radioactive sources to specific cancer sites. In permanent brachytherapy, the radioactive source is sealed within a protective capsule to create a brachytherapy seed ready for implantation (see Figure 2). Titanium is the most common material used for conventional seeds as it provides structural integrity to the seed so that it remains in situ whilst also preventing the escape of the radioactive source [37]. The use of titanium also allows for MRI-guided insertion enabling improved accuracy of placement, which can be performed by remotely controlled afterloading devices, removing the need for manual handling and insertion of radioactive sources. Automation of this procedure can improve the accuracy of the therapy alongside significantly reducing radiation exposure to clinicians [38]. New seed and applicator devices continue to be developed along with alternative materials to address different clinical aspects associated with cancers at various body sites [39]. Improvements in applicator and seed design and geometry will allow for better visualisation from the various imaging modalities used, resulting in more accurate implantation and retention, which in turn will translate to more accurate and effective dosimetry at the target site. Custom applicators and seed devices are also desirable when conventional devices fail to conform or adapt to patient specific anatomy [40].

One novel brachytherapy implant device that has been developed is CivaSheet® (CivaTech, Durham, NC). Unlike traditional seed implants, CivaSheet is comprised of a flexible, planar bioabsorbable membrane which contains multiple unidirectional radioactive sources, known as CivaDots, fixed within its proprietary polymer matrix at regular intervals (see Figure 3) [41]. The 103Pd radiation source is placed on top of a thin gold shield which imparts directional radiation that can selectively target cancerous tissue whilst sparing healthy tissue on the shielded side. The gold disc serves to shield the radiation and as a radiopaque marker that can be visualised using CT imaging [42]. The device also enables clinicians to utilise custom sizes of the device and the malleable nature of its planar membrane means it can conform to various physiological structures depending on the location of tumour and the patients’ anatomy. This device can be applied intraoperatively during tumour resection and can also be administered via less invasive methods during a treatment regimens [43]. As within any brachytherapy device, the dosimetric characteristics of the source must be established and requires numerous in silico, in vitro and in vivo studies to ascertain the feasibility of new devices [44].

Click to view original image

Figure 3 (a) Schematic of the cross-section of a CivaDot and its composition. (b) Illustration of a CivaSheet brachytherapy device. The CivaDots are orientated within the bioabsorbable membrane to provide unidirectional radiation. Adapted with permission from © Wiley [45].

One issue with permanent brachytherapy seeds, is that in certain instances they can require surgical removal. Sano et al. investigated the use of biocompatible, injectable thermos-responsive polymer labelled with 90Y [46]. Poly (2-alkyl-2-oxazoline) (POZ) is an isomeric polypeptide material synthesised via the cationic ring-opening polymerisation of 2-oxazolines [47]. Modifications of the 2-substituent of the 2-oxazoline monomer allowed for modifications to the POZ polymer sidechains. POZ derivatives have a low critical solution temperature (LCST), and can self-aggregate above a specific transition temperature (Tt) that is determined by oxazoline composition and molecular weight of its polymers [48]. Sano et al. utilised the thermo-responsive characteristic of POZ derivatives to create polymers that were soluble at room temperature and upon intratumoral injection, rapidly self-aggregated into rigid structures retained within the tumour. The enhanced permeability and retention effect demonstrated to cause POZ accumulation within tumours and the ability to label a radioactive source to the polymer facilitated their potential use as injectable materials for brachytherapy (see Figure 4) [49].

Click to view original image

Figure 4 Concept of injectable, thermo-responsive, radioisotope labelled polymers that aggregate within tumours for brachytherapy applications. This research was originally published in JNM © SNMMI [46].

Rhenium loaded silicate-based glass seeds is another material that has been investigated for brachytherapy administration. Utilising the sol-gel processing method it was possible to incorporate stoichiometric amounts of rhenium within silicate-based glasses (with formulation 20% rhenium, 50% silicon and 30% calcium, neither weight nor mole % was provided) and fabricate seeds of a predetermined geometry [50]. 186Re has a relatively short half-life of 16.9 hours and offers the possibility of releasing high energy β-emission over a short time period in comparison to other radionuclides with longer half-lives [51]. Knowing the geometry of the seed, the energy generated per seed and the dosimetric factors of the source, it was possible to calculate the number and location of seeds required to be placed in order to deliver effective brachytherapy to a tumour. Several rhenium based radiotherapy treatments are currently in early phases of clinical trials investigating the utility of 186Re and 188Re isotopes [52]. 186Re has a lower β-emission than 188Re with a maximum tissue penetration of 4.5 mm and a half-life of 3.6 days, making 186Re an ideal candidate for treating small to mid-sized tumours. The larger tissue penetration depth of 188Re, maximum of 11 mm, and its shorter half-life means that it could be employed for the treatment of larger tumours over a short time period [51]. Radiotherapy from 188Re sources has been investigated for medullary carcinomas of the head and neck [53], hepatocellular carcinomas [54] and for brachytherapy of basal or squamous cell carcinomas [55].

An alternative device to typical brachytherapy seeds was the use of conical-shaped needles, similar to those used in microneedle arrays for transdermal drug delivery, to penetrate into solid tumours to deliver intratumoral doses of radiation. Kim et al. investigated using titanium (Ti) and molybdenum (Mo) needles coated using pulsed laser deposition or chemical vapour deposition with holmium (Ho) or rhenium (Re) that following neutron activation readily yield therapeutic radionuclides [56]. 166Ho is produced following irradiation of 165Ho in a neutron flux and decays to emit high energy, tumoricidal β-particles. 186Re and 188Re are also both β-emitters and like 166Ho also emit photons (x-rays and γ-rays) which can be detected using Single Photon Emission Computer Tomography (SPECT) facilitating their use as theranostic agents [57]. Pulsed laser depositions was used to ablate Ho foil within a vacuum using an intense pulsed laser causing the formation of a Ho plasma plume that condensed on to Ti needles. Ti was chosen as the needle material due to its high biocompatibility and strength as well as the ease at which needles of specific sizes and geometries can be fabricated. Importantly, Ti produces a very low amount of radioactive isotopes, following neutron activation, that are deemed negligible and unable to cause significant cellular damage, further validating the choice of material [58]. Despite the ability to control the amount of Ho coated onto Ti needles and therefore tailor the amount of radioactivity, Ho deposition was found to dissociate from the needle when in acidic conditions that mimicked the intracellular environment of solid tumours. In the same study, Re of varying thickness (25, 75 and 125 µM) was uniformly deposited on Mo needles by chemical vapor deposition. This process involved passing a rhenium pentachloride containing precursor vapour over a heated Mo needle. Stability studies demonstrated only minimal leaching of radioactive Re was observed in neutral and acidic (pH 3.5) environments. Unlike Ti, following neutron irradiation Mo produces undesirable radionuclides and daughter isotopes that would have to be considered when calculating radiation dosimetry for patients. In order to prevent the generation of such radionuclides, a gadolinium (Gd) shield was created that housed the base of the device to absorb neutrons. The very high neutron cross-section of Gd prevents the Mo base from neutron activation, whilst allowing the protruding Re-coated Mo needle to become radioactive [59]. These neutron-activated biomaterials offer the possible to provide personalised internal radiotherapy treatment by optimisation of the needle material, geometry and quantity, the thickness of radionuclide coating as well as the radionuclides used based upon the size and location of the tumour to be treated. The advantageous nuclear properties of Ho and Re, such as their high neutron capture cross-sections, half-lives and resultant radionuclides upon decay make them attractive elements to form theranostic devices.

4. Polymeric Biomaterials, Applicators and Spacers

The benefits of radiotherapy when combined with the surgical resection of breast tumours for example, has been validated in multiple clinical studies and is considered a preferential breast conservation therapy in early stage breast cancer [60]. Accelerated partial breast irradiation (APBI) involves radiotherapy targeted directly to the lumpectomy bed and a 1-2 cm margin as opposed to radiotherapy delivered to the entire breast [61]. This process spares adjacent healthy tissue and enables a higher dose of radiation to be delivered to the target in a shorter treatment period. Combination therapy has been shown to decrease local recurrence of cancer as well as improve overall survival rates in patients with early-stage breast cancer [62]. Several different approaches have been employed to deliver the radiotherapy including intra operative radiation therapy and conformal EBRT although multicatheter interstitial brachytherapy and balloon catheter brachytherapy are most commonly used [63]. For these procedures and other types of temporary brachytherapy, catheters are used to place radioactive sources within an applicator into a predetermined location for a set period of time.

The development of flexible polymer-based catheters and applicators that are able to accurately place, using image-guided techniques and afterloading equipment, to retain radioactive sources in the correct location and orientation have been central to the progression of therapies such as APBI [64]. Numerous polymers such as silicone, nylon, polyurethane, polyethylene terephthalate (PET) and thermoplastic elastomers are utilised for the generation of commercially available and custom catheters. The combination of polymeric components provides desirable characteristics and can be manufactured and tailored for specific applications [65]. Polymer based devices that have multiple regions where a radioactive source can be accurately placed that derive from a single entry device are now common practise within the clinic [66]. Devices such as the Strut Adjusted Volume Implant [67] device (Cianna Medical, California) comprises of a central strut encircled by either 6, 8 or 10 peripheral struts and ClearPath (North American Scientific, California), where inner and outer catheters can be independently expanded to give varying expansion radii, are becoming more prevalent due to their enhanced ability to conform to the lumpectomy cavity during APBI [68,69]. The combination of radio-opaque markers located within the peripheral struts and the ability to differentially load the struts with high-dose radiation sources facilitate accurate treatment processes [70]. The catheters are inserted at predetermined distances between them to ensure sufficient coverage of the lumpectomy region plus an acceptable margin [64].

Balloon catheter brachytherapy is routinely used in APBI and are similar in respect to multicatheter devices in that they are single entry devices that are expanded to provide conformance of the lumpectomy cavity to the balloon. The MammoSite® (Hologic, Massachusetts) and the Contura balloon device (SenoRX, California) are FDA approved brachytherapy devices and consists of a silicone balloon connected to a dual-lumen catheter which controls the inflation and delivery of the radioactive source [71,72]. A saline solution containing control material is used to inflate the balloon to the desired diameter and 192Ir can be remotely after-loaded into the device at the prescribed radiation dose. The diameter of the inflated balloon, the distance of the balloon to the skin and the dose distribution are all interrelated factors that must be considered in order for effective treatment using this method [73]. Axxent electron brachytherapy system (Xoft, California) is another balloon-based applicator that differs slightly in that an electronic 50 kilo-voltage x-ray source is used to deliver radiation as opposed to 192Ir. Since an x-ray tube is used within the balloon catheter this process eliminates the need for a high dose rate afterloader and the use of a shielded vault meaning that this procedure may be more accessible for some patients [74].

Researchers continue to develop novel balloon applicator designs that are able to increase the therapeutic effect they have whilst in situ [75]. Balloon applicators designed using alternative biomaterials at their interface have been investigated for localised delivery of therapeutic payloads. The added treatment intervention can be seamlessly integrated into conventional treatment practise as they do not compromise the primary function of the balloon applicators or require additional interventional procedures. Ouyang et al. investigated coating balloon applicators with a degradable polymer film that could release cerium oxide nanoparticles (CONPs) to act as radical scavengers during APBI (Figure 5) [76]. An inherent feature of radiotherapy is its inability to discriminate between healthy and cancerous tissue which leads to unwanted adverse effects. The radiation-induced generation of reactive oxygen species (ROS), such as hydroxyl radicals (OH·) and hydrogen peroxide (H2O2), can cause unrepairable DNA damage to healthy and cancerous cells [77]. CONPs have been have shown to be capable of the catalytic removal of ROS and thereby could help to protect normal cells from ROS-induced apoptosis [78]. The selective protection is driven by the pH dependence of the CONP induced catalysis and normal cells have a neutral intracellular environment whereas cancerous cells tend to be acidic [79]. Ouyang et al. proposed that CONPs could diffuse from polymer films as they degrade within the body and accumulate in the surrounding tissue of the lumpectomy cavity. The rate of diffusion into the tissue could be tailored by the concentration of CONPs and the degradation rate of the polymer film so that the radioprotective effect could be matched to the radiation schedule to increase the effectiveness of treatment [76].

Click to view original image

Figure 5 Schematic of a potential balloon applicator that is coated with a polymer film loaded with cerium oxide nanoparticles for radioprotection of healthy tissue during accelerated partial breast irradiation.

One method used in brachytherapy, as well as in EBRT, to achieve maximal tumour radiation dose whilst limiting the exposure of surrounding healthy tissue is the incorporation of radioprotective spacers. Spacers are surgically positioned into predetermined locations and manually displace healthy tissues and adjacent organs from the tumour. When the radiation source is active at the tumour site, healthy tissues are pushed further away and therefore receives a lower absorbed dose [80]. This helps to alleviate damage to healthy tissue and reduce radiation-induced adverse events. Spacers are predominantly, although not exclusively, used in cancers of the abdominal and pelvic regions and are widespread in the treatment of cervical and prostate cancer due to the relative ease of implantation [81]. The size, shape and material used for radiotherapy spacers is dependent on the anatomical site of the tumour. Natural materials such as human collagen [82] and hyaluronic acid [83] have been investigated as spacers due to their biocompatibility and biodegradability. Although the preliminary clinical indications on the use of hyaluronic acid and human collagen were encouraging, hyaluronic acid was found to be unstable when exposed to radiation and highly viscous making accurate injection a technical challenge, whereas the availability of human collagen has limited its utilisation [84]. Polyethylene-glycol (PEG) hydrogel is a non-toxic, non-immunogenic and bioresorbable material and is commonly employed as a radioprotective spacer for use in prostate cancer treatment [85]. SpaceOAR™ (Augmenix Inc., Waltham, MA) is currently the only FDA approved hydrogel for use in prostate cancer radiation therapy [86]. The hydrogel is placed between the rectum and the prostate, thereby controlling the spatial distribution and accuracy of radiation from brachytherapy seeds within the prostate, whilst decreasing rectal damage during radiotherapy (see Figure 6). Spacers can be used in brachytherapy as well as being utilised in EBRT, in particular in conjunction with stereotactic body radiotherapy (SBRT), where the large fraction sizes used suggest that there is a greater need to protect adjacent healthy tissue from damage [87]. In similar studies, PEG hydrogel micro particles containing covalently bound iodine have been investigated as radiopaque fiducial markers and spacers for gynecologic and pancreatic cancer treatment [80,88]. The presence of iodine enables it to be visible using CT, cone beam computer topography and mammography whilst the high water content of the hydrogel makes it visible via MRI and ultrasound. It has therefore been proposed that hydrogels such as this could be accurately placed in regions between the head of the pancreas and the radiosensitive duodenum to allow dose escalations of radiotherapy in cases of unresectable pancreatic cancer [80].

Click to view original image

Figure 6 Axial T2 MRI images of a patient (a) prior to hydrogel spacer injection, (b) post implantation. Reproduced with permission from [89].

Domb et al. developed biodegradable balloons as alternative devices capable of acting as spacers that can displace the irradiated prostate away from the surrounding tissues, such as the rectal wall, in patients undergoing radiotherapy for prostate carcinoma. Biodegradable PLCL polymers are used to fabricate the biodegradable balloons (bio-balloons) which can be inserted via a minimally invasive procedure through the perineum in a deflated, rolled up conformation before being inflated in situ to form a structure with a defined size and volume [90]. The bio-balloons were designed to remain inflated and to retain their structural integrity over a period that exceeds the radiotherapy treatment, typically around 6 weeks, but fully degrade in the body within a year with no residual parts of the device remaining in situ. Both the polymer of choice and the methodology used to fabricate the balloon were vital in creating the device with the desired physical and mechanical properties. The balloons needed to be formed from a highly homogenous, flexible and elastic material that maintains its mechanical properties whilst folded prior to inflation and also whilst inflated in vivo. Poly-l-lactide-co- ε-caprolactone (PLCL) was the polymer used since this had the necessary mechanical properties and had an optimum degradation profile that was shorter than other polyhydroxyacid based biomaterials, such as polycaprolactone (PCL) [91]. The bio-balloons were fabricated using a dip coating technique in order for the balloons to be formed from a continuous single unit that minimised the number of connecting parts and regions where parts were joined/glued. Regions such as these are susceptible to deformation and leakages that could cause premature deflation of the bio-balloons in situ. An agarose mould of the desired size and shape of the bio-balloon and its nozzle was first formed and subsequently dipped into a polymer solution containing 14% w/v of PLCL in the organic solvent dichloromethane. This was performed under a dry nitrogen atmosphere to prevent condensation forming on the PLCL layer whilst the solvent evaporated. The agarose mould underwent three successive cycles of dipping and drying to fabricate balloons with an optimal and homogenous wall thickness of ~100 µm. Following completion of the dip coating, the agar mould is removed by dissolving in distilled water at 90°C and squeezed out of the balloon nozzle [92]. The balloon is then sterilised using ethylene oxide, in order to retain its chemical and mechanical stability, and can be implanted into the desired region in vivo, inflated using physiological saline and sealed using a PLCL plug to displace the irradiated prostate from surrounding healthy tissue. Clinical trials have demonstrated the safety of the bio-balloons and their ability to increase the rectal-prostate interspace from 0.22 ± 0.2 cm to 2.47 ± 0.47cm throughout the duration of radiotherapy [93]. The separation decreased the radiation exposure to the rectum, thereby reducing the adverse events and facilitating dose escalation of the radiotherapy to improve treatment efficacy.

Endorectal balloons made from silicon or latex have also been routinely employed to physically move the dose-limiting structure of the rectum during prostate cancer radiotherapy and to reduce prostate motion during treatment [94]. Endorectal balloons have the potential to change the dose exposure of surrounding healthy tissue but can increase exposure to the anterior rectal wall meaning accurate and controlled placement is vital [95]. Parsai et al. developed a novel, detractable device to temporarily displace the rectum to prevent damage during treatment of tumours in the pelvic cavity [96]. A Nitinol shape memory wire was placed inside a clinical approved endorectal balloon that could be activated by joule heating and controlled through an electrical conductor that produces thermal energy as current passes through it. The Nitinol wire functions as an actuator that allows the shape of the device to be tailored in situ to accurately move the organs adjacent to the body cavity in specific directions. Nitinol is a nickel-titanium alloy that is biocompatible and commonly used for medicinal and orthopaedic applications and displays biomimetic actuation due to a reversible crystalline phase transformation. Nitinols unique reversible shape memory property is due to its two crystalline structures: martensite and austenite [97]. Prior to insertions of the endorectal balloon device, Nitinol is soft and flexible due to its martensite phase. Once inserted, barium is injected to allow proper localisation of the balloon where it can then be inflated and orientated into the correct position. Nitinol is than actuated via joule heating causing the transformation of the Nitinol to its austenitic phases, thereby causing the Nitinol wire to change its shape. This results in the controlled movement of the balloon device that displaces the posterior rectum wall and a subsequent movement of the anterior rectum wall away from the proposed radiation field. Following the completion of HDR brachytherapy or EBRT, a reduction in temperature causes the Nitinol to return to its original martensitic phase and shape so that the device can be deflated and removed from the patient with minimal discomfort. Devices such as this have the potential to alleviate morbidities to the rectum and facilitate the delivery of escalated, ablative dose of radiation to tumours.

Currently, the majority of image-guided brachytherapy procedures routinely use inert radiotherapy biomaterials for devices such as spacers, seeds and their applicators. The sole purpose of these inert biomaterials is to ensure geometric accuracy for the duration of therapy in order for a predictable and calculated dose of radiation to be achieved at the cancerous site. Recent studies have investigated developing a new generation of radiotherapy biomaterials that are multifunctional and capable of enhancing current treatment and delivering additional therapeutic effects [98]. These ‘smart’ biomaterials are being designed to be responsive to specific stimuli, such as temperature or pH, and responding directly to cancer induced changes due to the conditions of the tumour micro-environment. Innovative smart biomaterials can have an active response or change in structure thereby facilitating additional functions that could enhance treatment, such as targeted drug delivery or initiation of an immune response [99].

Although spacers have become critical components for accurate radiation delivery, they provide no direct therapeutic benefit. The close proximity of the spacer to the tumour site has driven the rationale that this may also be harnessed for in situ delivery of therapeutic payloads to the cancer cells. Kumar et al. [100] developed Implantable Nanoplatforms for Chemo-Radiation Therapy (INCeRT) spacers formed using PLGA polymer matrix containing silica nanoparticles (with a size of 254 ± 5 nm) embedded within. These spacers were biocompatible with the same dimensions as clinically used spacers. The nanoparticles acted as drug/fluorophore depots that were released from the PLGA matrix due to its dissolution within the body. The nanoparticles then released encapsulated cargo upon interaction with biological fluid enabling the local delivery of therapeutics in a controlled and sustained manner. Nanoparticles have the added ability to passively target cancerous tissue and accumulate within tumours for an extensive time period due to the enhanced permeability and retention (EPR) effect [101]. Nanoparticles, such as those used on the INCeRT spacers, that can encapsulate both therapeutic and diagnostic payloads can allow for the qualitative assessment and extent of drug distribution within the tumour. Such methods could allow for a targeted, high dose of drug to be delivered with greater spatial distribution within the tumour. A delivery system like this could offer benefits over many typical chemotherapy regimens where systemic toxicities prevent their use throughout the duration of radiotherapy. The synergistic effect of radiation and chemotherapy could also be enhanced if effective radiosensitisation of the target tissue could be achieved whilst simultaneously sparing the neighbouring healthy tissue [102].

Polymers are attractive materials for sustained use or controlled release of therapeutic payloads due to multiple parameters that can be altered to create an optimal release profile. The molecular weight and the specific polymer used as well as type, concentration and size of payload can be tailored to customise the loading and release rates [103]. Synchronising the radiosensitisation or radioprotective effects of the payload with the radiation dosage could produce superior therapeutic efficacy [100]. Materials that facilitate this and increase the biodistribution of the payload to the target allow for optimisation of individual radiotherapy schedules and are therefore hugely desirable [104]. Many radiosensitising and radioprotective agents suffer from poor bioavailablity and rapid metabolism, along with having high systemic toxicity and therefore must be delivered in a controlled and targeted manner.

Utilising biomaterials for radiotherapy to deliver nanoparticles that either achieve radiosensitisation of surrounding tissue producing a radiation boost or those that can act as radioprotectants continues to be an area of intense research [105]. Nanoparticles can be fabricated to contain various different payloads and numerous techniques have been explored to incorporate them into and within existing biomaterials. Despite this, issues still remain regarding the use and delivery of sufficient concentrations of nanoparticles to the tumour site or surrounding tissue if this is the intended target. Nanoparticles that do not reach their target site could end up in systemic circulation, resulting in off-target effects that could be detrimental to the patients’ health [106].

5. Glass Biomaterials and Selective Internal Radiation Therapy

Bioactive glasses differ from non-bioactive glasses as they are able to form a continuous interface with host tissue upon implantation in the body without triggering fibrosis. This phenomenon has led to extensive investigations into their use for a range of potential therapeutic applications. The ability to tailor the glass properties by altering the composition of the glass with network modifiers and modifying oxides has been fundamental to these studies [107]. Alterations in the glass formulation affect the glasses physico-chemical and mechanical properties, bioactivity and dissolution rate. Novel glass formulations have been developed to improve the properties and to enhance the clinical translatability of bioactive glasses in order for them to address specific medical needs and elicit therapeutic responses [108].

The versatility of bioactive glasses have led to them being investigated for use in radiotherapy since various radionuclides that emit alpha, beta or gamma radiation can be chemically incorporated into their structure. Beta-emitting radionuclides have been most extensively studied due to their ability to deliver tumoricidal doses of radiation with sufficient levels of tissue penetration [109]. The properties of the radionuclide can be used to identify the best candidate to deliver the desired dose of radiation, over the appropriate distance, to achieve effective treatment of a specific organ or tissue [110]. During the manufacturing and processing procedure, the non-radioactive radionuclide is incorporated into the chemical and physical structure of the glass. Various processing techniques can be used to fabricate bioactive glasses into an array of different practical morphologies [107]. The ability to tailor the size and shape of bioactive glass microspheres facilitates their transport and delivery to specific locations to provide in situ radiotherapy. These glass microspheres are irradiated (i.e. made radioactive) by neutron activation of the radionuclides. Since neutron activation is the last step of the manufacturing process this provides an inherent safety benefit during glass fabrication. The time from activation to when they are actually delivered to clinic for administration can also be used to ensure the radiation dose required is provided to the patient.

Selective internal radiation therapy (SIRT) (also known as radioembolisation) is one method that has been employed to treat unresectable hepatocellular carcinoma to great effect. The proximity of the liver to adjacent critical organs can prevent the use of conventional EBRT [111]. SIRT is a form of internal radiotherapy that involves the delivery of radioactive microspheres to selectively irradiate tumours within the liver. The radioactive microspheres are administered via the hepatic arteries due to the fact that normal liver cells are predominantly vascularised by portal venous flow whereas cancer cells almost exclusively receive arterial blood. The liver vascularisation therefore results in the preferential deposition of these microspheres within hepatic tumours due to their increased vascularity (see Figure 7) [112]. Following administration, the microspheres migrate to and become trapped in hepatic vasculature supplying the tumour. The proximity of the microspheres to the tumour results in localised delivery of lethal doses of radiation to the tumour whilst sparing healthy parenchyma [113]. The microspheres can simultaneously cause a degree of embolisation by occluding the blood vessels to prevent blood and nutrient flow to the tumour [114]. There are currently two commercially available, FDA approved 90Y containing products used for SIRT [115]. TheraSphere (BTG International, London, United Kingdom) are alumina silicate glass microspheres, whereas SIR-Spheres (Sirtex Medical, Sydney, Australia) are resin-based microspheres. 90Y is used as it is a pure β-emitter with a tissue penetration depth ranging from 2.5-11 mm, capable of delivering therapeutic doses of ionising radiation. Despite the differences in physico-mechanical properties between the two different materials, both types of microspheres have exhibited comparable efficacy in clinical trials [116].

The 90Y containing resin-based SIR-spheres were developed in the late 1980s and approved by U.S. Food and Drug Administration in 2002 for the treatment of hepatic metastases secondary to colorectal adenocarcinoma [117]. SIR-spheres are comprised of a proprietary biocompatible microsphere that is coated with a cross-linked cation exchange polystyrene resin. 89Y is integrated into and immobilised within the resin matrix via ion exchange of sodium for yttrium followed by its precipitation as a phosphate salt. This prevents 90Y leaching out of the microspheres, following neutron activation, to a level that would be deemed to be physiological important in vivo [118].

Click to view original image

Figure 7 Schematic of SIRT and the use of radioactive microspheres for the treatment of liver cancer. Microspheres are administered via a catheter into the hepatic vasculature. Microspheres emit beta radiation to the tumour cells whilst having an embolic effect to further induce tumour apoptosis. Reproduced with permission from [119].

Traditional melt-quenching technique involving 89Y, aluminium oxide and silicon dioxide is used, followed by flame-spheroidisation for Therasphere glass microsphere manufacture [115]. The yttrium alumina silicate glass microspheres are composed of 17.1 mol% Y2O3, 18.9 mol% Al2O3 and 64.0 mol% SiO2 and range from 20-30 µm in diameter (see Table 2). The microspheres are non-toxic, non-biodegradable and chemically resistant to body fluids [120]. These glass microspheres undergo neutron bombardment which causes 89Y to be transduced into the β-emitter 90Y whilst the other elements within the glass remain non-radioactive. The 90Y-doped aluminosilicate glass microspheres demonstrate high chemical durability, which is essential for neutron activation and prevention of 90Y leakage [121]. Since the yttrium is incorporated in the glass structure and not a surface coating, it can only leach out of the glass and the target organ if the microspheres degrade in vivo during the time its radioactive [122]. The half-life of 90Y isotope is 2.7 days meaning that the radioactivity of the microspheres declines to a negligible level within 21 days from initial neutron bombardment [123].

Table 2 Characteristics of commercially available 90Y containing microspheres used in Selective Internal Radiation Therapy. Adapted from [124].

Phosphate-based glass microspheres have also been investigated for radiotherapy applications. The use of phosphate based glasses is advantageous due to their relatively low melting point to allow ease of manufacture and post processing techniques into different practical morphologies. Alteration to the composition of phosphate glasses have been shown to control their degradation rate over several orders of magnitude, ranging from minutes, days, months to years [125]. This makes them attractive resorbable materials to be implanted into the body that can be tailored to degrade in vivo at a rate that is optimum for a specific clinical application. Non-degradability is the main disadvantage of currently available silicate glass microspheres for SIRT as the glass microspheres would remain in the body as an impurity in the target area after radioactive decay of 90Y [126].

31P can also be neutron activated into the β-emitter 32P, which has a half-life 14.3 days [126]. 32P could potentially provide localised radiotherapy and enable the possibility of being incorporated into the glass structure of the microspheres simultaneously with another radionuclide such as 90Y. Masakazu et al. studied the effect of phosphorous ion implantation into a number of yttrium containing silica glasses to examine the possibility of enhancing their radiotherapeutic effect due to the longer half-life of 32P. Whilst high chemical durability was obtained, phosphorous can be a problem for some silicate glasses as it plays an integral role in nucleation of crystalline phases [127]. Sene et al. investigated the effect of phosphate glass microspheres (P2O5-Al2O3-SiO2-MgO) for radiotherapy application and found that the glass composition 42P2O5-12Al2O3-4SiO2-44MgO (in weight%) showed the best chemical durability and resistance to crystallisation, displaying the feasibility of using phosphate-based glass microspheres for radiotherapy applications [128]. The high durability of ceramic yttrium phosphate microspheres, composed of Y2O3 and YPO4, have also been explored as potential materials capable of delivering radiotherapy [126]. Glass microspheres made from alumina borate glass doped with rhenium have also been considered for in vivo radioembolisation therapy since rhenium is composed of two isotopes (185Re and 187Re) that can be converted to beta-emitting 186Re and 188Re radioisotope respectively, after neutron bombardment (see Table 3) [129].

Prior to microsphere administration during SIRT, a diagnostic angiography is conducted to assess the vasculature of the liver and tumour. Technetium-99m macroaggregated albumin (99mTc-MAA) particles, that are comparable in size to the 90Y microspheres, are injected as a scout dose and their distribution within the liver studied. Due to 99mTc emitting readily detectable gamma rays, single-photon emission CT (SPECT) can be used to estimate the dose to the tumour and surrounding parenchyma and to evaluate the potential of pulmonary and extrahepatic shunting [130]. Although 99mTc-MAA SPECT dosimetry is accurate for SIRT, alternate methods are being developed that can combine the therapeutic radiotherapy with the ability to simultaneously achieve diagnostic information at the tumour site. This theranostics based approach could provide real time information on the biodistribution of radiotherapeutic agents within a tumour, help determine the optimal dose and monitor the response to treatment [131].

Barros Filho et al. explored the use of holmium doped phosphate-based glass microspheres as alternative materials for SIRT that could also provide theranostic potential [132]. Traditional melt-quenching method was used to prepare these glasses followed by flame spheroidisation or gravitational falling within a furnace was performed to obtain microspheres of the desired geometry (see Table 3). Neutron activated 166Ho is comparable to 90Y in that it is a β-emitter, with a mean tissue penetration of around 2.5 mm, although it has a significantly reduced half-life of 26.8 hours [133]. The advantage of using 166Ho is that it is also a gamma emitter, meaning that it can be detected using SPECT, as well as its paramagnetic properties allowing for Magnetic Resonance Imaging [35,134]. These clinical imaging techniques could facilitate the real time visualisation of the holmium-doped microspheres during and post-treatment and can be used to quantitatively measure 166Ho distribution in vivo [133,135].

Radioactive 166Ho loaded poly(L-lactic acid) (PLLA) microspheres (166Ho-PLLA) (QuiremSpheres®, Quirem Medical B.V., The Netherlands) have been developed as an alternative to glass microspheres for SIRT [136,137]. The use of 166Ho-PLLA has the potential to eliminate the need of a scout dose, such 99mTc-MAA, followed by a therapeutic dose since the 166Ho-PLLA microspheres are capable of performing both roles concurrently. The diagnostic feature of 166Ho-PLLA could enable monitoring of intrahepatic behaviour of the microspheres during and post treatment [138]. Knowledge of the amount of microspheres that reach the cancerous and normal liver tissue of each patient allows clinicians to adjust the treatment plan accordingly and identify tumours that may be receiving an inadequate dose [139]. Poly(lactic acid) microspheres that contain 30 weight% rhenium for liver cancer treatment have also been investigated. Polymers susceptibility to degradation due to the use of high neutron fluxes during neutron activation and the difficulty in achieving a high enough activity to produce a therapeutic effect must be circumvented when developing microspheres for SIRT [140].

Currently, research has predominantly focused on glasses containing only a single radioactive element that can be used to deliver in situ radiation to cancerous tissue. It is feasible that glasses could be prepared containing multiple elements that can become radionuclides following neutron activation of the glass. The radionuclides could simultaneously irradiate the target tissue and the differences in half-lives and emission energies could be utilised to optimise the radiation delivered to the tumour, dependent on it its size and location [141].

Table 3 Materials used to fabricate microspheres and investigated for in situ delivery of radiation therapy.

6. Bone Cements and Radiotherapy for the Treatment of Spinal Metastases

Vertebral metastases are a common manifestation of many cancers and the proximity of vertebral metastases to the spinal cord can result in debilitating pain as well as severe neurological complications in the event of vertebral collapse. In cases of metastatic spinal cord compressions, the treatment regimens must address the tumour itself as well as restoring the structural integrity of the vertebrae [147]. Vertebroplasty or kyphoplasty is performed in such instances and are surgical procedures involving the injection of a bone cement into the vertebral body to restore strength. This is conventionally followed by multiple session of external beam radiation therapy to control and arrest tumour growth as well as providing pain relief. Despite advances in conformal EBRT, concerns about the safety of this technique arise due to potential irradiation of adjacent radiosensitive spinal cord tissue [148]. An alternative approach that has been considered is the incorporation of radionuclides into the bone cement.

Polymethylmethacrylate (PMMA) is the most commonly used material to form bone cement due to its good mechanical properties and its ability to be administered via a minimally invasive percutaneous procedure [149]. Donanzam et al. investigated combining PMMA with calcium phosphate ceramics that contained β-emitting radionuclides integrated within their structure as novel biomaterial to treat spinal metastases [150]. Calcium phosphate based biomaterials have been extensively studied for bone repair and regeneration due to their bioactivity, osteoconductive properties and similarity of their chemical composition to that of bone [151]. They offer flexibility in their composition and synthesis by techniques such as sol-gel and melt quenching. In their work, Donanzam et al. formed composite PMMA with multiphasic calcium phosphates that incorporated either holmium or samarium. Upon neutron activation the radioisotopes 166Ho and 153Sm were produced with activates calculated to be 32.5 and 14.5 MBq/mg, which was considered to be clinically suitable for site specific radiotherapy. PMMA injection itself was believed to have antitumour effects which were driven by the exothermic reaction of its polymerisation in vivo. The hyperthermia induced death of the tumour cells and its neovascular network can arrest tumour growth in addition to the bone cement inhibiting the region in which the tumour can grow into. The synergistic effect of PMMA cement and radiotherapy is anticipated to lead to a more efficacious treatment [152]. Other radionuclides such as 32P, 188Re and 153Sa have also been investigated as radionuclides that could augment the symptomatic relief provided by vertebroplasty to patients with vertebral metastases [153,154]. Although preliminary studies, biomaterials such as these provide a novel approach to integrate radiotherapy with vertebroplasty to form a convenient, single treatment procedure with enhanced clinical benefits over a sustained period [155].

The incorporation of radionuclides onto or within the structure of various biomaterials can facilitate the targeted and sustained delivery of radiotherapy to cancerous tissue. Each radionuclide has their own characteristic energy spectrum and particle emission [153]. The different particle energies and half-lives can be utilised to increase the spatial-temporal localisation of radiation and be used to customise the length and intensity of the absorbed radiation dose received (see Table 4). Sophisticated software and modelling programs can be used to predict the dose distribution from the radionuclide source, or combination of different sources, and can evaluate the suitability of potential new treatment methods.

Table 4 Characteristics of β-emitting radionuclides that have been investigated for the in situ delivery of radiation therapy. Mev, mega-electronvolts; keV, kilo-electronvolts.

7. Utilising Biomaterials for Targeted Drug Delivery during Radiotherapy

The synergistic effect of chemotherapy and radiotherapy has the potential to enhance cancer treatment efficacy and a consequential reduction in the treatment time for patients. Chemotherapy is commonly employed as an adjuvant therapy prior and following radiotherapy to enhance its tumorcidal ability. Chemotherapy is predominantly administered systemically and is often non-selective, which can cause radiosensitivity of healthy tissue and therefore limits drug dosage and potential efficacy [160]. Strategies involving the use of biomaterials have been adopted capable of delivering chemotherapeutics in a site-specific manner to increase the efficacy of radiotherapy.

Gliomas are the most prevalent form of brain tumour and require intratumoral delivery of chemotherapeutics during radiotherapy in order to reduce toxicity to surrounding critical tissue and to circumvent the blood brain barrier [161]. Liang et al. investigated the use of oxidised hyaluronic acid/adipic acid dihydrazide (oxi-HA/ADH) hydrogel as a biocompatible, thermogelling material to be used for the targeted, sustained delivery of the antineoplastic agent carboplatin [162]. The oxi-HA/ADH hydrogel was injected intratumorally in a cool liquid form, where it then configured into a gel-like matrix at body temperature within 1 to 8 minutes depending on operational temperatures. The hydrophilic carboplatin was administered with the hydrogel and retained in the matrix structure following crosslinking. The naturally occurring hyaluronidase enzymes can gradually degrade the hydrogel facilitating the sustained release of carboplatin. Carboplatin forms inter-strand and intra-strand cross links with purine bases of DNA causing inhibition of DNA repair and therefore augmented radiation-induced DNA damage and subsequent apoptosis [163].

Biomaterials that are responsive to radiation are being developed for novel approaches such as drug delivery vehicles at sites being irradiated. Fan et al. synthesised a gamma radiation-responsive amphiphilic polymer with tellurium-containing side-chains (PEG-b-PAA-g-Te) for targeted drug delivery [164]. Tellurium-containing compounds have been explored as anticancer agents since they are capable of increasing intracellular oxidative stress, generating ROS and converting less-reactive-ROS into higher reactive species [165]. The PEG-b-PAA-g-Te polymer coordinated with anticancer agent cisplatin and was self-assembled in an aqueous solution. This resulted in cisplatin being retained in the hydrophobic core of the polymer nanoparticles. The coordination of the two anticancer agents provisionally reduced their cytotoxic effects and thereby reduced to an extent some of the adverse off-target effects associated when administered. A low dosage of gamma radiation caused the tellurium side-chain of the polymer to become oxidised. This oxidation increased the hydrophilicity of the polymer and caused the nanoparticles to disassemble. The oxidation and subsequent disassembly caused weakening of the coordination between cisplatin and the tellurium, resulting in both compounds being exposed and able to elicit their cytotoxic tumour effects [164]. Cisplatin inhibits DNA replication and repair during the S phase of cell cycle and can therefore enhance radiation-induced apoptosis of irradiated cancer cells [166]. The material is responsive to the radiation and can enhance the delivery of anticancer agents in a site-specific manner whilst sparing the tissue that is not-being irradiated to reduce off target effects.

It has been well established that elevated levels of ROS are produced within cells following targeted radiation of cancerous tissue which is succeeded by intracellular reoxygenation post irradiation [35]. Utilising the high oxidative reactivity of ROS has been explored as an internal stimulus to selectively enhance drug delivery within irradiated tumours. Liu et al. developed ROS-responsive poly(tehiodiethylene adipate) (PSDEA) and PEG-PSDEA-PEG polymers as a drug delivery system to synergistically enhance the efficacy of radiotherapy by local ROS-activated chemotherapy [167]. The PSDEA and PEG-PSDEA-PEG polymers were synthesised into drug loaded nanoparticles via a nanoprecipitation method and self-assembly. This resulted in the encapsulation of hydrophobic anticancer camptothecin analogue, SN38, within the polymer nanoparticles, by hydrophobic association, thereby enhancing the stability of the drug under physiological conditions. The hydrophobic sulphide residues of the polymer chains were found to undergo ROS-mediated oxidation into hydrophilic sulfoxide groups. As a result, polymer nanoparticles experienced structural changes such as swelling and partial dissociation which caused significant unloading of SN38 from the nanoparticles (see Figure 8). In vivo studies showed that tumour growth was significantly inhibited in mice that received dual treatment modality of local X-ray irradiation in conjunction with intratumoral injection of SN38-loaded polymer nanoparticles when compared to either single treatment modality. This nanoparticle biomaterial system improves selective drug delivery by utilising nanoparticles preferential accumulation within tumours and alleviated issues associated with hydrophobic drug delivery [168]. Materials that respond to the local changes that radiotherapy, delivered internally or external, can induce to liberate drugs from their structure in a controllable manner can increase the spatio-temporal delivery of chemotherapeutics that have the ability to significantly improve the efficacy of radiotherapy.

Click to view original image

Figure 8 Schematic of the fabrication and mechanism by which ROS-responsive polymer nanoparticles can selectively release SN38 to synergistically enhance the efficacy of radiotherapy by local ROS-activated chemotherapy. Reproduced with permission from Copyright (2018) American Chemical Society [167].

Biomaterials can be used to augment current methods of radiation delivery and in many instances their use can be integrated in current treatment procedures. These biomaterial devices can be placed in close proximity to cancerous regions allowing the in situ delivery of radiation in a targeted manner. Novel biomaterials continue to be developed that can enhance the synergistic effect of other treatment modalities, such as chemotherapy and immunotherapy, and that can respond to various stimuli to deliver therapeutic payloads to target tissue to improve treatment efficacy.

8. Conclusions

The majority of improvements in EBRT have been as a result of technological advances in imaging modalities used to plan procedures and equipment to accurately deliver the radiation dose. Despite the ability to control their intensity and to modulate the shape of several beams from multiple angles, externally administered radiation has to pass through tissue to reach its target which can limit application and utility for treatment of certain cancers. Internal radiation is advantageous in that much larger localised doses of therapeutic radiation can be delivered using shorter range radionuclides. Polymer based materials, such as PEG hydrogels, have been explored to displace adjacent healthy tissue to prevent radiation-induced toxicities and as drug delivery vehicles to locally administer chemotherapeutics to enhance radiotherapy. Glass-based biomaterials doped with radionuclides, such as 90Y and 166Ho, have been developed and processed into microspheres capable of selectively irradiating tumours following their implantation into the body. These alpha, beta or gamma producing radionuclides have been chemically incorporated into glass compositions and the ability to process glass into desired sizes and practical morphologies facilitates their transport and delivery to specific target locations to provide in situ radiotherapy. Theranostic materials capable of providing diagnostic information whilst simultaneously delivering a therapeutic effect to enhance radiotherapy continue to be developed. Enhancing conventionally employed biomaterials, such as PMMA bone cements, to also deliver radiation has the potential to improve cancer treatment efficacy. New biomaterials continue to be developed to enhance the synergistic effect of other treatment modalities, such as chemotherapy and immunotherapy, by responding to radiation-induced stimuli and providing localised delivery of therapeutic payloads.


This work was supported by the Engineering and Physical Sciences Research Council (EPSRC) Thematic Studentship Centre for Doctoral Training in Bioinstructive Materials for Healthcare Applications [EP/R512321/1] through a doctoral training grant.

Author Contributions

BM: Writing-original draft preparation, Reviewing and Editing; AA: Writing-original draft preparation, IA, AT and RL: Conceptualisation, writing-reviewing and editing.


This work was supported by the Engineering and Physical Sciences Research Council (EPSRC) Thematic Studentship Centre for Doctoral Training in Bioinstructive Materials for Healthcare Applications [EP/R512321/1] through a doctoral training grant.

Competing Interests

The authors have declared that no competing interests exist.


  1. Atun R, Jaffray DA, Barton MB, Bray F, Baumann M, Vikram B, et al. Expanding global access to radiotherapy. Lancet Oncol. 2015; 16: 1153-1186. [CrossRef]
  2. Baskar R, Lee KA, Yeo R, Yeoh KW. Cancer and radiation therapy: Current advances and future directions. Int J Med Sci. 2012; 9: 193-199. [CrossRef]
  3. Wang JS, Wang Hj, Qian Hl. Biological effects of radiation on cancer cells. Mil Med Res. 2018; 5: 20. [CrossRef]
  4. Srinivas US, Tan BWQ, Vellayappan BA, Jeyasekharan AD. ROS and the DNA damage response in cancer. Redox Biol. 2019; 25: 101084. [CrossRef]
  5. Jackson SP, Bartek J. The DNA-damage response in human biology and disease. Nature. 2009; 461: 1071-1078. [CrossRef]
  6. Gregoire V. Tumor control probability (TCP) and normal tissue complication probability (NTCP) in head and neck cancer. Rays. 2005; 30: 105-108.
  7. Tang Q, Zhao F, Yu X, Wu L, Lu Z, Yan S. The role of radioprotective spacers in clinical practice: A review. Quant Imaging Med Surg. 2018; 8: 514-524. [CrossRef]
  8. Joubert A, Vogin G, Devic C, Granzotto A, Viau M, Maalouf M, et al. Radiation biology: Major advances and perspectives for radiotherapy. Cancer Rad. 2011; 15: 348-354. [CrossRef]
  9. Donahoe LL, Cho BJ, de Perrot M. Induction radiotherapy and mesothelioma surgery. Shanghai Chest. 2018; 2. [CrossRef]
  10. Baskar R, Dai J, Wenlong N, Yeo R, Yeoh KW. Biological response of cancer cells to radiation treatment. Front Mol Biosci. 2014; 1: 24. [CrossRef]
  11. Gaede S, Lock MI. Advances in external beam stereotactic body radiotherapy: Principle concerns in implementing a liver radiation program. Chin Clin Oncol. 2017; 6: S13. [CrossRef]
  12. Xu XG, Bednarz B, Paganetti H. A review of dosimetry studies on external-beam radiation treatment with respect to second cancer induction. Phys Med Biol. 2008; 53: R193-R241. [CrossRef]
  13. Ma CM, Maughan RL. Within the next decade conventional cyclotrons for proton radiotherapy will become obsolete and replaced by far less expensive machines using compact laser systems for the acceleration of the protons. Med Phys. 2006; 33: 571-573. [CrossRef]
  14. McDonald R, Chow E, Lam H, Rowbottom L, Soliman H. International patterns of practice in radiotherapy for bone metastases: A review of the literature. J Bone Oncol. 2014; 3: 96-102. [CrossRef]
  15. Chino F, Stephens SJ, Choi SS, Marin D, Kim CY, Morse MA, et al. The role of external beam radiotherapy in the treatment of hepatocellular cancer. Cancer. 2018; 124: 3476-3489. [CrossRef]
  16. Rehman Ju, Zahra, Ahmad N, Khalid M, Noor ul Huda Khan Asghar HM, Gilani ZA, et al. Intensity modulated radiation therapy: A review of current practice and future outlooks. J Radiat Res Appl Sc. 2018; 11: 361-367. [CrossRef]
  17. Shirato H, Le QT, Kobashi K, Prayongrat A, Takao S, Shimizu S, et al. Selection of external beam radiotherapy approaches for precise and accurate cancer treatment. J Radiat Res. 2018; 59: i2-i10. [CrossRef]
  18. Garibaldi C, Jereczek-Fossa BA, Marvaso G, Dicuonzo S, Rojas DP, Cattani F, et al. Recent advances in Radiat Oncol. Ecancermedicalscience. 2017; 11: 785. [CrossRef]
  19. Verbruggen A, Coenen HH, Deverre JR, Guilloteau D, Langstrom B, Salvadori PA, et al. Guideline to regulations for radiopharmaceuticals in early phase clinical trials in the EU. Eur J Nucl Med Mol. 2008; 35: 2144-2151. [CrossRef]
  20. Furubayashi N, Negishi T, Ura S, Hirai Y, Nakamura M. Palliative effects and adverse events of strontium-89 for prostate cancer patients with bone metastasis. Mol Clin Oncol. 2015; 3: 257-263. [CrossRef]
  21. Nicolas GP, Morgenstern A, Schottelius M, Fani M. New developments in peptide receptor radionuclide therapy. J Nucl Med. 2018; 60: 167-171. [CrossRef]
  22. Larson SM, Carrasquillo JA, Cheung NK, Press OW. Radioimmunotherapy of human tumours. Nat Rev Cancer. 2015; 15: 347-360. [CrossRef]
  23. Harrison MR, Wong TZ, Armstrong AJ, George DJ. Radium-223 chloride: A potential new treatment for castration-resistant prostate cancer patients with metastatic bone disease. Cancer Manag Res. 2013; 5: 1-14. [CrossRef]
  24. Bedard G, Chow E. The failures and challenges of bone metastases research in Radiat Oncol. J Bone Oncol. 2013; 2: 84-88. [CrossRef]
  25. Skowronek J. Current status of brachytherapy in cancer treatment - short overview. J Contemp Brachytherapy. 2017; 9: 581-589. [CrossRef]
  26. Faugeras L, Pirson AS, Donckier J, Michel L, Lemaire J, Vandervorst S, et al. Refractory thyroid carcinoma: Which systemic treatment to use? Ther Adv Med Oncol. 2018; 10: 1758834017752853. [CrossRef]
  27. Taheri M, Azizmohammadi Z, Ansari M, Dadkhah P, Dehghan K, Valizadeh R, et al. 153Sm-EDTMP and 177Lu-EDTMP are equally safe and effective in pain palliation from skeletal metastases. Nuklearmedizin. 2018; 57: 174-180. [CrossRef]
  28. Vinjamuri S, Gilbert TM, Banks M, McKane G, Maltby P, Poston G, et al. Peptide receptor radionuclide therapy with (90)Y-DOTATATE/(90)Y-DOTATOC in patients with progressive metastatic neuroendocrine tumours: assessment of response, survival and toxicity. Br J Cancer. 2013; 108: 1440-1448. [CrossRef]
  29. Ghilezan M, Martinez AA. Chapter 14 - Brachytherapy. In: Gunderson LL, Tepper JE, editors. Clinical Radiat Oncol (Third Edition). Philadelphia: W.B. Saunders; 2012; p. 259-286. [CrossRef]
  30. Chassagne D, Dutreix A, Almond P, Burgers JMV, Busch M, Joslin CA. Report 38. J Int Comm Rad Units Meas. 2016; os20: NP. Available from: [CrossRef]
  31. Mendez LC, Morton GC. High dose-rate brachytherapy in the treatment of prostate cancer. Transl Androl Urol. 2018; 7: 357-370. [CrossRef]
  32. Mukherjee A, Sarma HD, Saxena S, Kumar Y, Chaudhari P, Goda JS, et al. Bioevaluation of (125) I Ocu-Prosta seeds for application in prostate cancer brachytherapy. Indian J Med Res. 2014; 139: 555-560.
  33. Trindade BM, Christóvão MT, Trindade DdFM, Falcão PL, Campos TPRd. Dosimetria comparativa de braquiterapia de próstata com sementes de I-125 e Pd-103 via SISCODES/MCNP. Radiologia Brasileira. 2012; 45: 267-272. [CrossRef]
  34. Dieterich S, Ford E, Pavord D, Zeng J. Chapter 8 - Brachytherapy. In: Dieterich S, Ford E, Pavord D, Zeng J, editors. Rep Pract Oncol Radiother. Philadelphia: Elsevier. 2016; p. 108-122. [CrossRef]
  35. Dayal R, Singh A, Pandey A, Mishra K. Reactive oxygen species as mediator of tumor radiosensitivity. J Cancer Res Ther. 2014; 10: 811-818. [CrossRef]
  36. Lehmann T, Sloboda R, Usmani N, Tavakoli M. Model-based needle steering in soft tissue via lateral needle actuation. IEEE Robot Autom Lett. 2018; 3: 3930-3936. [CrossRef]
  37. Tanderup K, Viswanathan AN, Kirisits C, Frank SJ. Magnetic resonance image guided brachytherapy. Semin Radiat Oncol. 2014; 24: 181-191. [CrossRef]
  38. Aronowitz JN. Afterloading: The technique that rescued brachytherapy. Int J Radiat Oncol Biol Phys. 2015; 92: 479-487. [CrossRef]
  39. Zhou J, Zamdborg L, Sebastian E. Review of advanced catheter technologies in radiation oncology brachytherapy procedures. Cancer Manag Res. 2015; 7: 199-211. [CrossRef]
  40. Paterson DB, Pearson SM, Wilson AN. Intracavitary vaginal brachytherapy using a custom balloon applicator. J Med Radiat Sci. 2017; 64: 310-314. [CrossRef]
  41. Cohen GN, Episcopia K, Lim SB, LoSasso TJ, Rivard MJ, Taggar AS, et al. Intraoperative implantation of a mesh of directional palladium sources (CivaSheet): Dosimetry verification, clinical commissioning, dose specification, and preliminary experience. Brachytherapy. 2017; 16: 1257-1264. [CrossRef]
  42. Rivard MJ. A directional (103)Pd brachytherapy device: Dosimetric characterization and practical aspects for clinical use. Brachytherapy. 2017; 16: 421-432. [CrossRef]
  43. Zhen H, Turian JV, Sen N, Luu MB, Abrams RA, Wang D. Initial clinical experience using a novel Pd-103 surface applicator for the treatment of retroperitoneal and abdominal wall malignancies. Adv Radiat Oncol. 2018; 3: 216-220. [CrossRef]
  44. Aima M, DeWerd LA, Mitch MG, Hammer CG, Culberson WS. Dosimetric characterization of a new directional low-dose rate brachytherapy source. Med Phys. 2018; 45: 3848-3860.. [CrossRef]
  45. Aima M, Reed JL, DeWerd LA, Culberson WS. Air-kerma strength determination of a new directional (103)Pd source. Med Phys. 2015; 42: 7144-7152. [CrossRef]
  46. Sano K, Kanada Y, Kanazaki K, Ding N, Ono M, Saji H. Brachytherapy with intratumoral injections of radiometal-labeled polymers that thermoresponsively self-aggregate in tumor tissues. J Nucl Med. 2017; 58: 1380-1385. [CrossRef]
  47. de la Rosa VR. Poly(2-oxazoline)s as materials for biomedical applications. J Mater Sci Mater Med. 2014; 25: 1211-1225. [CrossRef]
  48. Luxenhofer R, Han Y, Schulz A, Tong J, He Z, Kabanov AV, et al. Poly(2-oxazoline)s as polymer therapeutics. Macromol Rapid Commun. 2012; 33: 1613-1631. [CrossRef]
  49. Kanazaki K, Sano K, Makino A, Homma T, Ono M, Saji H. Polyoxazoline multivalently conjugated with indocyanine green for sensitive in vivo photoacoustic imaging of tumors. Sci Rep. 2016; 6: 33798. [CrossRef]
  50. Khorshidi A, Ahmadinejad M, Hamed Hosseini S. Evaluation of a proposed biodegradable 188re source for brachytherapy application: A review of dosimetric parameters. Medicine. 2015; 94: e1098. [CrossRef]
  51. Lepareur N, Lacoeuille F, Bouvry C, Hindre F, Garcion E, Cherel M, et al. Rhenium-188 labeled radiopharmaceuticals: Current clinical applications in oncology and promising perspectives. Front Med. 2019; 6: 132. [CrossRef]
  52. Lambert B, Bacher K, Defreyne L, Gemmel F, Van Vlierberghe H, Jeong JM, et al. 188Re-HDD/lipiodol therapy for hepatocellular carcinoma: A phase I clinical trial. J Nucl Med. 2005; 46: 60-66. [CrossRef]
  53. Jürgens S, Herrmann WA, Kühn FE. Rhenium and technetium based radiopharmaceuticals: Development and recent advances. J Organomet Chem. 2014; 751: 83-89. [CrossRef]
  54. Nowicki ML, Cwikla JB, Sankowski AJ, Shcherbinin S, Grimmes J, Celler A, et al. Initial study of radiological and clinical efficacy radioembolization using 188Re-human serum albumin (HSA) microspheres in patients with progressive, unresectable primary or secondary liver cancers. Med Sci Monit. 2014; 20: 1353-1362. [CrossRef]
  55. Sedda AF, Rossi G, Cipriani C, Carrozzo AM, Donati P. Dermatological high-dose-rate brachytherapy for the treatment of basal and squamous cell carcinoma. Clin Exp Dermatol. 2008; 33: 745-749. [CrossRef]
  56. Kim J, Narayan RJ, Lu X, Jay M. Neutron-activatable needles for radionuclide therapy of solid tumors. J Biomed Mater Res A. 2017; 105: 3273-3280. [CrossRef]
  57. Hamoudeh M, Kamleh MA, Diab R, Fessi H. Radionuclides delivery systems for nuclear imaging and radiotherapy of cancer. Adv Drug Deliv Rev. 2008; 60: 1329-1346. [CrossRef]
  58. Kulkarni M, Mazare A, Schmuki P. Biomaterial surface modification of titanium and titanium alloys for medical applications. Nanomedicine. 2014; p. 111-136.
  59. Leinweber G, Barry DP, Trbovich MJ, Burke JA, Drindak NJ, Knox HD, et al. Neutron capture and total cross-section measurements and resonance parameters of gadolinium. Nucl Sci Eng. 2006; 154: 261-279. [CrossRef]
  60. Clarke M, Collins R, Darby S, Davies C, Elphinstone P, Evans V, et al. Effects of radiotherapy and of differences in the extent of surgery for early breast cancer on local recurrence and 15-year survival: An overview of the randomised trials. Lancet. 2005; 366: 2087-2106. [CrossRef]
  61. Njeh CF, Saunders MW, Langton CM. Accelerated partial breast irradiation (APBI): A review of available techniques. Radiat Oncol. 2010; 5: 90. [CrossRef]
  62. Guidolin K, Lock M, Vogt K, McClure JA, Winick-Ng J, Vinden C, et al. Recurrence and mortality after breast-conserving surgery without radiation. Curr Oncol. 2019; 26: 380-388. [CrossRef]
  63. Bennion NR, Baine M, Granatowicz A, Wahl AO. Accelerated partial breast radiotherapy: A review of the literature and future directions. Gland Surg. 2018; 7: 596-610. [CrossRef]
  64. Dickler A, Patel RR, Wazer D. Breast brachytherapy devices. Expert Rev Med Devices. 2009; 6: 325-333. [CrossRef]
  65. Barde M, Davis M, Rangari S, Mendis HC, De La Fuente L, Auad ML. Development of antimicrobial-loaded polyurethane films for drug-eluting catheters. J Appl Polym Sci. 2018; 135: 46467. [CrossRef]
  66. Scanderbeg D, Yashar C, White G, Rice R, Pawlicki T. Evaluation of three APBI techniques under NSABP B-39 guidelines. J Appl Clin Med Phys. 2009; 11: 3021. [CrossRef]
  67. Tesavibul P, Felzmann R, Gruber S, Liska R, Thompson I, Boccaccini AR, et al. Processing of 45S5 Bioglass® by lithography-based additive manufacturing. Mater Lett. 2012; 74: 81-84. [CrossRef]
  68. Manoharan SR, Rodriguez RR, Bobba VS, Chandrashekar M. Dosimetry evaluation of SAVI-based HDR brachytherapy for partial breast irradiation. J Med Phys. 2010; 35: 131-136. [CrossRef]
  69. Beriwal S, Coon D, Kim H, Haley M, Patel R, Das R. Multicatheter hybrid breast brachytherapy: A potential alternative for patients with inadequate skin distance. Brachytherapy. 2008; 7: 301-304. [CrossRef]
  70. Yashar C, Mahmood U. Strut-adjusted volume implant: A targeted radiation treatment in breast cancer. Future Oncol. 2010; 6: 1813-1816. [CrossRef]
  71. Edmundson GK, Vicini FA, Chen PY, Mitchell C, Martinez AA. Dosimetric characteristics of the MammoSite RTS, a new breast brachytherapy applicator. Int J Radiat Oncol Biol Phys. 2002; 52: 1132-1139. [CrossRef]
  72. Ojeda-Fournier H, Olson LK, Rochelle M, Hodgens BD, Tong E, Yashar CM. Accelerated partial breast irradiation and posttreatment imaging evaluation. RadioGraphics. 2011; 31: 1701-1716. [CrossRef]
  73. Bensaleh S, Bezak E, Borg M. Review of MammoSite brachytherapy: Advantages, disadvantages and clinical outcomes. Acta Oncol. 2009; 48: 487-494. [CrossRef]
  74. Dickler A, Dowlatshahi K. Xoft Axxent electronic brachytherapy. Expert Rev Med Devices. 2009; 6: 27-31. [CrossRef]
  75. Schmid MP, Berger D, Heilmann M, Bor J, Wisgrill B, Azizi-Semrad U, et al. Inflatable multichannel rectal applicator for adaptive image-guided endoluminal high-dose-rate rectal brachytherapy: Design, dosimetric characteristics, and first clinical experiences. J Contemp Brachytherapy. 2017; 9: 359-363. [CrossRef]
  76. Ouyang Z, Mainali MK, Sinha N, Strack G, Altundal Y, Hao Y, et al. Potential of using cerium oxide nanoparticles for protecting healthy tissue during accelerated partial breast irradiation (APBI). Phys Med. 2016; 32: 631-635. [CrossRef]
  77. Azzam EI, Jay-Gerin JP, Pain D. Ionizing radiation-induced metabolic oxidative stress and prolonged cell injury. Cancer Lett. 2012; 327: 48-60. [CrossRef]
  78. Wason MS, Colon J, Das S, Seal S, Turkson J, Zhao J, et al. Sensitization of pancreatic cancer cells to radiation by cerium oxide nanoparticle-induced ROS production. Nanomedicine. 2013; 9: 558-569. [CrossRef]
  79. Wason MS, Lu H, Yu L, Lahiri SK, Mukherjee D, Shen C, et al. Cerium Oxide nanoparticles sensitize pancreatic cancer to radiation therapy through oxidative activation of the JNK apoptotic pathway. Cancers. 2018; 10. [CrossRef]
  80. Rao AD, Feng Z, Shin EJ, He J, Waters KM, Coquia S, et al. A novel absorbable radiopaque hydrogel spacer to separate the head of the pancreas and duodenum in radiation therapy for pancreatic cancer. Int J Radiat Oncol Biol Phys. 2017; 99: 1111-1120. [CrossRef]
  81. Padmanabhan R, Pinkawa M, Song DY. Hydrogel spacers in prostate radiotherapy: A promising approach to decrease rectal toxicity. Future Oncol. 2017; 13: 2697-2708. [CrossRef]
  82. Noyes WR, Hosford CC, Schultz SE. Human collagen injections to reduce rectal dose during radiotherapy. Int J Radiat Oncol Biol Phys . 2012; 82: 1918-1922. [CrossRef]
  83. Kishi K, Iida T, Ojima T, Sonomura T, Shirai S, Nakai M, et al. Esophageal gel-shifting technique facilitating eradicative boost or reirradiation to upper mediastinal targets of recurrent nerve lymph node without damaging esophagus. J Radiat Res. 2013; 54: 748-754. [CrossRef]
  84. Schutzer ME, Orio PF, Biagioli MC, Asher DA, Lomas H, Moghanaki D. A review of rectal toxicity following permanent low dose-rate prostate brachytherapy and the potential value of biodegradable rectal spacers. Prostate Cancer Prostatic Dis. 2015; 18: 96-103. [CrossRef]
  85. Pinkawa M, Corral NE, Caffaro M, Piroth MD, Holy R, Djukic V, et al. Application of a spacer gel to optimize three-dimensional conformal and intensity modulated radiotherapy for prostate cancer. Radiother Oncol. 2011; 100: 436-441. [CrossRef]
  86. Song DY, Herfarth KK, Uhl M, Eble MJ, Pinkawa M, van Triest B, et al. A multi-institutional clinical trial of rectal dose reduction via injected polyethylene-glycol hydrogel during intensity modulated radiation therapy for prostate cancer: analysis of dosimetric outcomes. Int J Radiat Oncol Biol Phys. 2013; 87: 81-87. [CrossRef]
  87. Susil RC, McNutt TR, DeWeese TL, Song D. Effects of prostate-rectum separation on rectal dose from external beam radiotherapy. Int J Radiat Oncol Biol Phys. 2010; 76: 1251-1258. [CrossRef]
  88. Bair RJ, Bair E, Viswanathan AN. A radiopaque polymer hydrogel used as a fiducial marker in gynecologic-cancer patients receiving brachytherapy. Brachytherapy. 2015; 14: 876-880. [CrossRef]
  89. Vanneste BGL, Pijls-Johannesma M, Van De Voorde L, van Lin EN, van de Beek K, van Loon J, et al. Spacers in radiotherapy treatment of prostate cancer: Is reduction of toxicity cost-effective? Radiother Oncol. 2015; 114: 276-281. [CrossRef]
  90. Levy Y, Paz A, Yosef RB, Corn BW, Vaisman B, Shuhat S, et al. Biodegradable inflatable balloon for reducing radiation adverse effects in prostate cancer. J Biomed Mater Res B Appl Biomater. 2009; 91: 855-867. [CrossRef]
  91. Haim Zada M, Kumar A, Elmalak O, Markovitz E, Icekson R, Domb AJ. In vitro and in vivo degradation behavior and the long-term performance of biodegradable PLCL balloon implants. Int J Pharm. 2020; 574: 118870. [CrossRef]
  92. Basu A, Haim-Zada M, Domb AJ. Biodegradable inflatable balloons for tissue separation. Biomaterials. 2016; 105: 109-116. [CrossRef]
  93. Gez E, Cytron S, Ben Yosef R, London D, Corn BW, Alani S, et al. Application of an interstitial and biodegradable balloon system for prostate-rectum separation during prostate cancer radiotherapy: A prospective multi-center study. Radiat Oncol. 2013; 8: 96. [CrossRef]
  94. Serrano NA, Kalman NS, Anscher MS. Reducing rectal injury in men receiving prostate cancer radiation therapy: Current perspectives. Cancer Manag Res. 2017; 9: 339-350. [CrossRef]
  95. Elsayed H, Bolling T, Moustakis C, Muller SB, Schuller P, Ernst I, et al. Organ movements and dose exposures in teletherapy of prostate cancer using a rectal balloon. Strahlenther Onkol. 2007; 183: 617-624. [CrossRef]
  96. Parsai EI, Jahadakbar A, Lavvafi H, Elahinia M. A novel and innovative device to retract rectum during radiation therapy of pelvic tumors. J Appl Clin Med Phys. 2019; 20: 194-199. [CrossRef]
  97. Elahinia M. Shape memory alloy actuators: Design, fabrication and experimental evaluation. 2nd ed. New Jersey: Wiley; 2016. [CrossRef]
  98. Ngwa W, Boateng F, Kumar R, Irvine DJ, Formenti S, Ngoma T, et al. Smart radiation therapy biomaterials. Int J Radiat Oncol Biol Phys. 2017; 97: 624-637. [CrossRef]
  99. Moreau M, Yasmin-Karim S, Kunjachan S, Sinha N, Gremse F, Kumar R, et al. Priming the abscopal effect using multifunctional smart radiotherapy biomaterials loaded with immunoadjuvants. Front Oncol. 2018; 8: 56. [CrossRef]
  100. Kumar R, Belz J, Markovic S, Jadhav T, Fowle W, Niedre M, et al. Nanoparticle-based brachytherapy spacers for delivery of localized combined chemoradiation therapy. Int J Radiat Oncol Biol Phys. 2015; 91: 393-400. [CrossRef]
  101. Mi Y, Shao Z, Vang J, Kaidar-Person O, Wang AZ. Application of nanotechnology to cancer radiotherapy. Cancer Nanotechnol. 2016; 7: 11. [CrossRef]
  102. Lawrence TS, Blackstock AW, McGinn C. The mechanism of action of radiosensitization of conventional chemotherapeutic agents. Semin Radiat Oncol. 2003; 13: 13-21. [CrossRef]
  103. Stuart MA, Huck WT, Genzer J, Muller M, Ober C, Stamm M, et al. Emerging applications of stimuli-responsive polymer materials. Nat Mater. 2010; 9: 101-113. [CrossRef]
  104. Ngwa W, Kumar R, Sridhar S, Korideck H, Zygmanski P, Cormack RA, et al. Targeted radiotherapy with gold nanoparticles: Current status and future perspectives. Nanomedicine. 2014; 9: 1063-1082. [CrossRef]
  105. Wang H, Mu X, He H, Zhang XD. Cancer radiosensitizers. Trends Pharmacol Sci. 2018; 39: 24-48. [CrossRef]
  106. Boateng F, Ngwa W. Delivery of Nanoparticle-based radiosensitizers for radiotherapy applications. Int J Mol Sci. 2019; 21. [CrossRef]
  107. Islam MT, Felfel RM, Abou Neel EA, Grant DM, Ahmed I, Hossain KMZ. Bioactive calcium phosphate-based glasses and ceramics and their biomedical applications: A review. J Tissue Eng. 2017; 8: 2041731417719170. [CrossRef]
  108. Rabiee SM, Nazparvar N, Azizian M, Vashaee D, Tayebi L. Effect of ion substitution on properties of bioactive glasses: A review. Ceram Int. 2015; 41: 7241-7251. [CrossRef]
  109. Mosconi C, Cappelli A, Pettinato C, Golfieri R. Radioembolization with Yttrium-90 microspheres in hepatocellular carcinoma: Role and perspectives. World J Hepatol. 2015; 7: 738-752. [CrossRef]
  110. Baino F, Hamzehlou S, Kargozar S. Bioactive Glasses: Where Are We and Where Are We Going? J Funct Foods. 2018; 9: 25. [CrossRef]
  111. Nijsen JF, van het Schip AD, Hennink WE, Rook DW, van Rijk PP, de Klerk JM. Advances in nuclear oncology: microspheres for internal radionuclide therapy of liver tumours. Curr Med Chem. 2002; 9: 73-82. [CrossRef]
  112. Edeline J, Gilabert M, Garin E, Boucher E, Raoul JL. Yttrium-90 microsphere radioembolization for hepatocellular carcinoma. Liver Cancer. 2015; 4: 16-25. [CrossRef]
  113. Molvar C, Lewandowski R. Yttrium-90 radioembolization of hepatocellular carcinoma-performance, technical advances, and future concepts. Seminars Int Radiol. 2015; 32: 388-397. [CrossRef]
  114. Popperl G, Helmberger T, Munzing W, Schmid R, Jacobs TF, Tatsch K. Selective internal radiation therapy with SIR-Spheres in patients with nonresectable liver tumors. Cancer Biother Radiopharm. 2005; 20: 200-208. [CrossRef]
  115. Westcott MA, Coldwell DM, Liu DM, Zikria JF. The development, commercialization, and clinical context of yttrium-90 radiolabeled resin and glass microspheres. Adv Radiat Oncol. 2016; 1: 351-364. [CrossRef]
  116. Van Der Gucht A, Jreige M, Denys A, Blanc-Durand P, Boubaker A, Pomoni A, et al. Resin versus glass microspheres for 90Y transarterial radioembolization: Comparing survival in unresectable hepatocellular carcinoma using pretreatment partition model dosimetry. J. Nucl. Med. 2017; 58: 1334-1340. [CrossRef]
  117. Hendlisz A, Van den Eynde M, Peeters M, Maleux G, Lambert B, Vannoote J, et al. Phase III trial comparing protracted intravenous fluorouracil infusion alone or with yttrium-90 resin microspheres radioembolization for liver-limited metastatic colorectal cancer refractory to standard chemotherapy. J Clin Oncol. 2010; 28: 3687-3694. [CrossRef]
  118. Gray BNC, AU), inventor; Sirtex Medical Limited (North Ryde, AU), assignee. Polymer based radionuclide containing particulate material. United States; 2014.
  119. De La Vega JC, Esquinas PL, Rodríguez-Rodríguez C, Bokharaei M, Moskalev I, Liu D, et al. Radioembolization of hepatocellular carcinoma with built-in dosimetry: First in vivo results with uniformly-sized, biodegradable microspheres labeled with 188Re. Theranostics. 2019; 9: 868-883. [CrossRef]
  120. Christie JK, Tilocca A. Short-range structure of yttrium alumino-silicate glass for cancer radiotherapy: Car–parrinello molecular dynamics simulations. Adv Eng Mater. 2010; 12: B326-B330. [CrossRef]
  121. Erbe EM, Day DE. Chemical durability of Y2O3-Al2O3-SiO2 glasses for the in vivo delivery of beta radiation. J Biomed Mater Res. 1993; 27: 1301-1308. [CrossRef]
  122. Christie JK, Malik J, Tilocca A. Bioactive glasses as potential radioisotope vectors for in situ cancer therapy: investigating the structural effects of yttrium. Phys. Chem. Chem. Phys. 2011; 13: 17749-17755. [CrossRef]
  123. Kennedy A, Brown DB, Feilchenfeldt J, Marshall J, Wasan H, Fakih M, et al. Safety of selective internal radiation therapy (SIRT) with yttrium-90 microspheres combined with systemic anticancer agents: expert consensus. J Gastrointest Oncol. 2017; 8: 1079-1099. [CrossRef]
  124. Mahnken AH. Current status of transarterial radioembolization. World J Radiol. 2016; 8: 449-459. [CrossRef]
  125. Ahmed I, Lewis M, Olsen I, Knowles JC. Phosphate glasses for tissue engineering: Part 1. Processing and characterisation of a ternary-based P2O5–CaO–Na2O glass system. Biomaterials. 2004; 25: 491-499. [CrossRef]
  126. Kawashita M, Shineha R, Kim HM, Kokubo T, Inoue Y, Araki N, et al. Preparation of ceramic microspheres for in situ radiotherapy of deep-seated cancer. Biomaterials. 2003;24(17):2955-2963. [CrossRef]
  127. Kawashita M, Miyaji F, Kokubo T, Takaoka GH, Yamada I, Suzuki Y, et al. Surface structure and chemical durability of P+-implanted Y2O3–Al2O3–SiO2 glass for radiotherapy of cancer. J Non Cryst Solids. 1999; 255: 140-148. [CrossRef]
  128. Sene FF, Martinelli JR, Okuno E. Synthesis and characterization of phosphate glass microspheres for radiotherapy applications. J Non Cryst Solids. 2008; 354: 4887-4893. [CrossRef]
  129. Conzone SD, Hafeli UO, Day DE, Ehrhardt GJ. Preparation and properties of radioactive rhenium glass microspheres intended for in vivo radioembolization therapy. J Biomed Mater Res. 1998; 42: 617-625. [CrossRef]
  130. Garin E, Rolland Y, Laffont S, Edeline J. Clinical impact of (99m)Tc-MAA SPECT/CT-based dosimetry in the radioembolization of liver malignancies with (90)Y-loaded microspheres. Eur J Nucl Med Mol Imaging. 2016; 43: 559-575. [CrossRef]
  131. Degrauwe N, Hocquelet A, Digklia A, Schaefer N, Denys A, Duran R. Theranostics in interventional oncology: Versatile carriers for diagnosis and targeted image-guided minimally invasive procedures. Front Pharmacol. 2019; 10: 450. [CrossRef]
  132. Barros Filho EC, Martinelli JR, Squair PL, Osso Junior JA, Sene FF, editors. Development and evaluation of holmium doped phosphate glass microspheres for selective internal radiotherapy. INAC 2013: International nuclear atlantic conference; 2013; Brazil.
  133. Bult W, Kroeze SG, Elschot M, Seevinck PR, Beekman FJ, de Jong HW, et al. Intratumoral administration of holmium-166 acetylacetonate microspheres: Antitumor efficacy and feasibility of multimodality imaging in renal cancer. PLoS One. 2013; 8: e52178. [CrossRef]
  134. Zielhuis SW, Nijsen JF, de Roos R, Krijger GC, van Rijk PP, Hennink WE, et al. Production of GMP-grade radioactive holmium loaded poly(L-lactic acid) microspheres for clinical application. Int J Pharm. 2006; 311: 69-74. [CrossRef]
  135. Smits ML, Elschot M, van den Bosch MA, van de Maat GH, van het Schip AD, Zonnenberg BA, et al. In vivo dosimetry based on SPECT and MR imaging of 166Ho-microspheres for treatment of liver malignancies. J Nucl Med. 2013; 54: 2093-2100. [CrossRef]
  136. van Roekel C, Smits MLJ, Prince JF, Bruijnen RCG, van den Bosch M, Lam M. Quality of life in patients with liver tumors treated with holmium-166 radioembolization. Clin Exp Metastasis 2020; 37: 95-105. [CrossRef]
  137. van de Maat GH, Seevinck PR, Elschot M, Smits ML, de Leeuw H, van Het Schip AD, et al. MRI-based biodistribution assessment of holmium-166 poly(L-lactic acid) microspheres after radioembolisation. Eur Radiol. 2013; 23: 827-835. [CrossRef]
  138. Smits ML, Nijsen JF, van den Bosch MA, Lam MG, Vente MA, Huijbregts JE, et al. Holmium-166 radioembolization for the treatment of patients with liver metastases: Design of the phase I HEPAR trial. J Exp Clin Cancer Res. 2010; 29: 70. [CrossRef]
  139. Radosa CG, Radosa JC, Grosche-Schlee S, Zophel K, Plodeck V, Kuhn JP, et al. Holmium-166 Radioembolization in hepatocellular carcinoma: Feasibility and safety of a new treatment option in clinical practice. Cardiovasc Intervent Radiol. 2019; 42: 405-412. [CrossRef]
  140. Hafeli UO, Roberts WK, Pauer GJ, Kraeft SK, Macklis RM. Stability of biodegradable radioactive rhenium (Re-186 and Re-188) microspheres after neutron-activation. Appl Radiat Isot. 2001; 54: 869-879. [CrossRef]
  141. Day DE. Glasses for radiotherapy. In: Baskar R, Lee KA, editors. Bio-Glasses. 63. NJ, USA: John Wiley & Sons. 2012; p.203-228. [CrossRef]
  142. Christie JK, Tilocca A. Molecular dynamics simulations and structural descriptors of radioisotope glass vectors for in situ radiotherapy. J Phys Chem B. 2012; 116: 12614-12620. [CrossRef]
  143. Ghahramani MR, Garibov AA, Agayev TN. Production and quality control of radioactive yttrium microspheres for medical applications. Appl Radiat Isot. 2014; 85: 87-91. [CrossRef]
  144. Miyazaki T, Tanaka T, Shirosaki Y, Kawashita M. Yttrium phosphate microspheres with enriched phosphorus content prepared for radiotherapy of deep-seated cancer. Ceram Int. 2014; 40: 15259-15263. [CrossRef]
  145. Kawashita M, Takayama Y, Kokubo T, Takaoka GH, Araki N, Hiraoka M. Enzymatic preparation of hollow yttrium oxide microspheres for in situ radiotherapy of deep-seated cancer. J Am Ceram Soc. 2006; 89: 1347-1351. [CrossRef]
  146. Poorbaygi H, Reza Aghamiri SM, Sheibani S, Kamali-asl A, Mohagheghpoor E. Production of glass microspheres comprising 90Y and 177Lu for treating of hepatic tumors with SPECT imaging capabilities. Appl Radiat Isot. 2011; 69: 1407-1414. [CrossRef]
  147. Zhao H, Shi Q, Sun ZY, Gu QL, Ni L, Yang HL. The importance of percutaneous vertebroplasty and radiation therapy for pathological vertebral compression fractures secondary to multiple myeloma. Arch Orthop Trauma Surg. 2012; 132: 1669-1670. [CrossRef]
  148. Li Y, Qing Y, Zhang Z, Li M, Xie J, Wang G, et al. Clinical efficacy of percutaneous vertebroplasty combined with intensity-modulated radiotherapy for spinal metastases in patients with NSCLC. Onco Targets Ther. 2015; 8: 2139-2145. [CrossRef]
  149. Vaishya R, Chauhan M, Vaish A. Bone cement. J Clin Orthop Trauma. 2013; 4: 157-163. [CrossRef]
  150. Donanzam BA, Campos TP, Dalmazio I, Valente ES. Synthesis and characterization of calcium phosphate loaded with Ho-166 and Sm-153: A novel biomaterial for treatment of spine metastases. J Mater Sci Mater Med. 2013; 24: 2873-2880. [CrossRef]
  151. Eliaz N, Metoki N. Calcium phosphate bioceramics: A review of their history, structure, properties, coating technologies and biomedical applications. Materials. 2017; 10. [CrossRef]
  152. Yang HL, Sun ZY, Wu GZ, Chen KW, Gu Y, Qian ZL. Do vertebroplasty and kyphoplasty have an antitumoral effect? Med Hypotheses. 2011; 76: 145-146. [CrossRef]
  153. Kaneko TS, Sehgal V, Skinner HB, Al-Ghazi MS, Ramsinghani NS, Marquez Miranda M, et al. Radioactive bone cement for the treatment of spinal metastases: A dosimetric analysis of simulated clinical scenarios. Phys Med Biol. 2012; 57: 4387-4401. [CrossRef]
  154. Cardoso ER, Ashamalla H, Weng L, Mokhtar B, Ali S, Macedon M, et al. Percutaneous tumor curettage and interstitial delivery of samarium-153 coupled with kyphoplasty for treatment of vertebral metastases. J Neurosurg Spine. 2009; 10: 336-342. [CrossRef]
  155. Montano CJ, de Campos TPR. Radioactive cement of pmma and HAP-Sm-153, Ho-166, OR RE-188 for bone metastasis treatment. Acta Ortop Bras. 2019; 27: 64-68. [CrossRef]
  156. Cheng Y, Kiess AP, Herman JM, Pomper MG, Meltzer SJ, Abraham JM. Phosphorus-32, a clinically available drug, inhibits cancer growth by inducing DNA double-strand breakage. PLoS One. 2015; 10: e0128152. [CrossRef]
  157. Muller C, Bunka M, Haller S, Koster U, Groehn V, Bernhardt P, et al. Promising prospects for 44Sc-/47Sc-based theragnostics: Application of 47Sc for radionuclide tumor therapy in mice. J Nucl Med. 2014; 55: 1658-1664. [CrossRef]
  158. Hao G, Mastren T, Hassan G, Silvers W, Oz O, Sun X. Reintroduction of copper-67 to radioimmunotherapy and evaluation of its imaging potential. J Nucl Med. 2017; 58: 940.
  159. Hindie E, Zanotti-Fregonara P, Quinto MA, Morgat C, Champion C. Dose deposits from 90Y, 177Lu, 111In, and 161Tb in micrometastases of various sizes: Implications for radiopharmaceutical therapy. J Nucl Med. 2016; 57: 759-764. [CrossRef]
  160. Dong HM, Wang Q, Wang WL, Wang G, Li XK, Li GD, et al. A clinical analysis of systemic chemotherapy combined with radiotherapy for advanced gastric cancer. Medicine (Baltimore). 2018; 97: e10786. [CrossRef]
  161. Lawrie TA, Evans J, Gillespie D, Erridge S, Vale L, Kernohan A, et al. Long-term side effects of radiotherapy, with or without chemotherapy, for glioma. Cochrane Database Syst Rev. 2018. [CrossRef]
  162. Liang HT, Lai XS, Wei MF, Lu SH, Wen WF, Kuo SH, et al. Intratumoral injection of thermogelling and sustained-release carboplatin-loaded hydrogel simplifies the administration and remains the synergistic effect with radiotherapy for mice gliomas. Biomaterials. 2018; 151: 38-52. [CrossRef]
  163. Wilson GD, Bentzen SM, Harari PM. Biologic basis for combining drugs with radiation. Seminars Radiat Oncol. 2006; 16: 2-9. [CrossRef]
  164. Fan F, Gao S, Ji S, Fu Y, Zhang P, Xu H. Gamma radiation-responsive side-chain tellurium-containing polymer for cancer therapy. Mater. Chem Front. 2018; 2: 2109-2115. [CrossRef]
  165. Seng HL, Tiekink ERT. Anti-cancer potential of selenium- and tellurium-containing species: Opportunities abound! Appl Organomet Chem. 2012; 26: 655-662. [CrossRef]
  166. Dasari S, Tchounwou PB. Cisplatin in cancer therapy: Molecular mechanisms of action. Eur J Pharmacol. 2014; 740: 364-378. [CrossRef]
  167. Liu TI, Yang YC, Chiang WH, Hung CK, Tsai YC, Chiang CS, et al. Radiotherapy-controllable chemotherapy from reactive oxygen species-responsive polymeric nanoparticles for effective local dual modality treatment of malignant tumors. biomacromolecules. 2018; 19: 3825-3839. [CrossRef]
  168. Tao W, He Z. ROS-responsive drug delivery systems for biomedical applications. Asian J Pharm Sci. 2018; 13: 101-112. [CrossRef]
Download PDF
0 0