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A new commercial 2D ionising radiation dosimeter (2Day.QA®) was developed. This work aims to introduce the basic functions of 2Day.QA®.The dosimeter is made mainly of a linear polysaccharide consisting of β(1 → 4) linked d-glucose units and radiation active substances, which make it environmentally friendly. For 2Day.QA® irradiation, radiotherapy ionising radiation sources were used. The analysis of 2Day.QA® was performed using three scanners: Vidar® Red LED Dosimetry Pro Advantage™, Vidar® VXR 12-plus™ and HP Scanjet G3010 flatbed scanner. The stability of 2Day.QA® was tested. Exemplary applications of 2DayQA® for QA studies of accelerator light and radiation field coincidence and brachytherapy source position were carried out.The dosimeter responded to the lowest applied dose of 0.95 Gy and saturated at over 94.9 Gy. The quasi-linear dose response is below 20 Gy. Vidar® Red LED Dosimetry Pro Advantage™ has proven to be superior to other scanners at determining dose effects in 2Day.QA®. The stability of the non-irradiated 2Day.QA® is at least 18 months. After 18 months of storage, the dosimeter reacted to irradiation. In the case of the irradiated samples, a slight color drift related to the absorbed dose was observed. Tests of the use of 2Day.QA® to control the quality of the accelerator light and radiation field coincidence and brachytherapy source position have shown that it can be used for such applications.The study reveals the potential of 2Day.QA® for 2D radiation dosimetry and concludes with recommendations for the use of the dosimeter for radiotherapy QA tests.

This work presents an approach to the fast determination of a medical accelerator irradiation isocenter as a quality assurance (QA) procedure in radiotherapy. The isocenter determination tool is the tissue equivalent high-resolution 3D polymer gel dosimeter (PABIGnx) in a dedicated container combined with kilovoltage imaging systems and the polyGeVero-CT software package (v. 1.2, GeVero Co., Poland). Two accelerators were employed: Halcyon and TrueBeam (Varian, USA), both equipped with cone beam computed tomography (CBCT) and iterative reconstruction CBCT (iCBCT) algorithms. The scope of this work includes: (i) the examination of factors influencing image quality (reconstruction algorithms and modes), radiation field parameters (dose and multi-leaf collimator (MLC) gaps), fiducial markers, signal averaging for reconstruction algorithms and the scanning time interval between consecutive scans, (ii) the examination of factors influencing the isocenter determination, image processing (signal averaging, background subtraction, image filtering) and (iii) an isocenter determination report using a 2D and 3D approach. An optimized protocol and isocenter determination conditions were found. The time and effort required to determine the isocenter are discussed.

This work presents the features of the PABIG

Purpose Advanced 3D dosimetry is required for verifications of complex dose distributions in modern radiotherapy. Two 3D polymer gel dosimeters, coupled with magnetic resonance (MR) imaging (3 T MRI) readout and data processing with polyGeVero® software, were tested for the verification of calculated 3D dose distributions by a treatment planning system (TPS) and ArcCHECK®–3DVH®, related to eradication of a lung tumour. Methods N-vinylpyrrolidone-containing 3D polymer gel dosimeters were used: VIC (containing ascorbic acid and copper sulfate pentahydrate) and VIC-T (containing tetrakis(hydroxymethyl)phosphonium chloride). Three remote centers were involved in the dosimeters preparation and irradiation (Poland), and MRI (Austria). Cross beam calibration of the dosimeters and verification of a 3D dose distribution calculated with an Eclipse External Beam TPS and ArcCHECK®–3DVH® were performed. The 3D-to-3D comparisons of the VIC and VIC-T with TPS and ArcCHECK®–3DVH® along with ArcCHECK®–3DVH® versus TPS dose matrixes were performed with the aid of the polyGeVero® by analyzing dose profiles, isodoses lines, gamma index, gamma angle, dose difference, and related histograms. Results The measured MR-relaxation rate (R2 = 1/T2) for the dosimeters relates to the dose, as follows: R2 = 0.0928 ± 0.0008 [Gy−1 s−1] × D [Gy] + 2.985 ± 0.012 [s−1] (VIC) and 0.1839 ± 0.0044 [Gy−1 s−1] × D [Gy] + 2.519 ± 0.053 [s−1] (VIC-T). The 3D-to-3D comparisons revealed a good agreement between the measured and calculated 3D dose distributions. Conclusions VIC and VIC-T with 3T MRI readout and polyGeVero® showed potential for verifications of calculated irradiation plans. The results obtained suggest the implementation of the irradiation plan for eradication of the lung tumour.

This paper aims to explain the phenomenon of laser light trapping (LLT) in a 3D polymer gel dosimeter. A VIC-T polymer gel dosimeter containing 17% N-vinylpyrrolidone, 8% N,N′-methylenebisacrylamide, 12% tert-butyl alcohol, 5% gelatine, 0.02% hydroquinone and 14 mM tetrakis(hydroxymethyl)phosphonium chloride was used in this study. It was exposed to green laser light with a wavelength of 532 nm. A film was recorded during the exposure. After exposure, Raman spectroscopy was used to study the reactions taking place inside the dosimeter. The obtained results were used to explain what the LLT phenomenon is, what are the consequences for the dosimeter in which such a phenomenon occurs, and what dosimeter components play an important role in the occurrence of LLT. In addition, the conditions under which 3D polymer gel dosimeters can be measured using optical computed tomography at short wavelengths of visible laser light are indicated.

In this work we discuss UV and ionising radiation induced processes in the flat foils (films). The foils were made from poly(vinyl alcohol) (PVA) and either 10,12-pentacosadiynoic acid (PDA) or a representative of tetrazolium salts − 2,3,5-triphenyl tetrazolium chloride (TTC). Also, we proposed a very attractive modification of the surfaces of the foils by vapour deposition of parylene C. This lead to an alteration of the UV dose response of the foils and improved their water-resistance thus making them potentially useful for radiation dose measurements when immersed in water. The TTC- and PDA-containing foils were shown to respond to ionising radiation in a high dose range of up to 3 kGy. The PDA foils were of a higher dose sensitivity and much lower dose threshold than those containing TTC. Whereas the TTC-containing foils were of irreversible character, those containing PDA showed high reversibility both to UV and ionising radiation. Basic features of such reversible-foil dosimeters are presented. Additionally, the mechanism of radiation induced changes in the TTC- and PDA-PVA films is analysed by using UV–vis spectrophotometry and Raman spectroscopy techniques.

This work reports on the results obtained for VIC-T dosimeter for radiotherapy dosimetry (17 % (w/v) N-vinylpyrrolidone, 8 % (w/v) N,N′-methylenebisacrylamide, 12 % (w/v) tert-butyl alcohol, 5 % (w/v) gelatine, 0.02 % (w/v) hydroquinone and 14 mM tetrakis (hydroxymethyl) phosphonium chloride (THPC)) measured with a spiral computed tomography (CT). Optimal spiral CT protocol, CT measurements conditions and image processing are provided. Basic features of VIC-T are discussed such as a calibration relation and dose resolution with respect to former N-vinylpyrrolidone containing dosimeters. Both adopted data processing performed with a new polyGeVero®-CT software package and its features are reported.

This work reports on the first results obtained for a new 3D lung mimicking dosimeter. The dosimeter comprises 3% (w/w) acrylamide, 3% (w/w) N,N′-methylenebisacrylamide, 10 mM tetrakis (hydroxymethyl) phosphonium chloride (THPC), 25% (w/w) poly(ethylene oxide)-block-poly (propylene oxide)-block-poly (ethylene oxide) (Pluronic F-127) in presence or absence of sodium chloride. The approach to the manufacturing of the dosimeter both in the presence of air and argon relied on the preparation of a foam using the surface-active properties of Pluronic F-127. The resistance of Pluronic F-127 matrix to irradiation was analysed using differential scanning calorimetry; however, the foam dosimeter after irradiation was measured by using Raman spectroscopy, scanning electron and optical microscopy as well as computed tomography. Preliminary investigation revealed the following: (i) sodium chloride improves the thermal properties of the foam dosimeter in a low temperature region and impacts on the foam density, (ii) the dosimeter prepared in presence and absence of air responds to irradiation, however, its dose response is improved in absence of air, (iii) the preparation method applied allowed for decreasing the density of the dosimeter relative to solid gel dosimeter towards the density of lungs tissue and lungs in exhale. The results obtained pointed to a potential of this new dosimeter in 3D radiotherapy dosimetry related to eradication of lung tumours.

A new radiochromic dosimeter was examined with Raman spectroscopy and an optical approach for assessment of 3D dose distribution integrity. The acronym of the dosimeter is Fricke-XO-Pluronic F-127, where XO denotes xylenol orange; Pluronic F-127 is a copolymer matrix of poly(ethylene oxide)-block-poly(propylene oxide)-block-poly(ethylene oxide), and the dosimeter contains the components of a Fricke dosimetric solution. Two dosimeter samples in cuvettes were partially irradiated such that a radiation dose was absorbed at the bottom of the cuvettes. After irradiation, one sample was stored upside down such that the irradiated part was at the top and another one was stored with the irradiated part at the bottom. Two diffusion coefficients of ferric ion complexes with XO ([XO-Fe]+3) were calculated. They were compared with those for similar dosimeter, however with gelatine matrix instead of Pluronic F-127. The results obtained indicate an impact of the gravitational force on the diffusion of [XO-Fe]+3ions over time after irradiation and thus a possibility of severely undermining the integrity of a dose distribution in irradiated dosimeter. The conclusions drawn suggest the necessity of examination of different 3D Fricke dosimeter compositions for anisotropic diffusion of ferric ions.

This work presents an improvement of the VIPARnd ('nd' stands for 'normoxic, double', or VIP) polymer gel dosimeter. The gel composition was altered by increasing the concentration of the monomeric components, N-vinylpyrrolidone (NVP) and N,N'-methylenebisacrylamide (MBA), in co-solvent solutions. The optimal composition (VIPARCT, where 'CT' stands for computed tomography, or VIC) comprised: 17% NVP, 8% MBA, 12% t-BuOH, 7.5% gelatine, 0.007% ascorbic acid, 0.0008% CuSO4 × 5H2O and 0.02% hydroquinone. The following characteristics of VIC were achieved: (i) linear dose range of 0.9_30 Gy, (ii) saturation for radiation doses of over 50 Gy, (iii) threshold dose of about 0.5 Gy, (iv) dose sensitivity of 0.171 Gy-1 s-1, which is roughly 2.2 times higher than that of VIP (for nuclear magnetic resonance measurements). It was also found that VIC is dose- rate-independent, and its dose response does not alter if the radiation source is changed from electrons to photons for external beam radiotherapy. The gel responded similarly to irradiation with small changes in radiation energy but was sensitive to larger energy changes. The VIC gel retained temporal stability from 20 h until at least 10 d after irradiation, whereas spatial stability was retained from 20 h until at least 6 d after irradiation. The scheme adopted for VIC manufacturing yields repeatable gels in terms of radiation dose response. The VIC was also shown to perform better than VIP using x-ray computed tomography as a readout method; the dose sensitivity of VIC (0.397 HU Gy-1) was 1.5 times higher than that of VIP. Also, the dose resolution of VIC was better than that of VIP in the whole dose range examined.

This work reports on the characteristic of a 3D polymer gel dosimeter with poly(ethylene oxide)-block-poly(propylene oxide)-block-poly(ethylene oxide) (Pluronic F-127) gel matrix. The dosimeter (acronym: VIP3-Pluronic F-127) comprises 4% (w/w) N-vinylpyrrolidone (NVP), 4% (w/w) N,N′-methylenebisacrylamide (MBA), 4% (w/w) tert-butanol, 10 mM tetrakis (hydroxymethyl)phosphonium chloride (THPC) and 25% (w/w) Pluronic F-127. A medical ionizing radiation source was used for irradiation of VIP3-Pluronic F-127 and the dosimeter was measured with a nuclear magnetic resonance (NMR, 0.47 T) relaxometer. The mean dose sensitivity of VIP3-Pluronic F-127 amounted to 0.1873 ± 0.0091 Gy−1 s−1, the intercept was equal to 1.3614 ± 0.0511 s−1, the linear dose response was in the range of 1–20 Gy, the dynamic dose range was of 1–50 Gy and the threshold dose was of ~1 Gy. The manufacturing process of VIP3-Pluronic F-127 was repeatable and the dosimeter was stable for at least 8 days after irradiation (no measurements for longer period were performed). It was also found that the dose response of VIP3-Pluronic F-127 is independent of the radiation dose rate and energy, and type of radiation (photons and electrons). The results obtained indicate that VIP3-Pluronic F-127 is promising as a polymer gel dosimeter for use in radiotherapy dosimetry.

Sophisticated techniques employed in radiotherapy for irradiation of tumours require comprehensive dosimetry allowing for precise, high resolution measurements of radiation dose distribution in three dimensions and verification of treatment planning systems. Polymer gel dosimetry has been shown to be a unique technique for three-dimensional high resolution measurements of absorbed radiation dose distributions. If exposed to ionizing radiation, radical polymerisation and crosslinking of monomeric components take place in a 3D polymer gel dosimeter, leading to the formation of large polymeric structures that scatter visible light. This feature allows for optical observation of the effects of the absorbed dose and its distribution. Presently, magnetic resonance imaging is employed the most often for analysis of 3D polymer gel dosimeters. However, much attention is also being given to the development of optical computed tomography since this technique is hoped to serve as a substitute for expensive and not easily available magnetic resonance imaging. The optical scanner presented in this work consists of a laser diode, a scanning system and a signal detector. A 3D polymer gel dosimeter is measured in an immersion liquid in order to reduce deflection of the light from the dosimeter phantom. The very first results were obtained with the newly constructed scanner for PABIGnx 3D polymer gel dosimeter, which was inhomogeneously irradiated with 192Ir brachytherapy source. The results have been contrasted with those for magnetic resonance imaging and are presented in this work together with the description of the optical scanner. Currently, optimization of the optical scanner is performed.

This work discusses the substitution of a gelatine physical gel matrix with a matrix made of poly(ethylene oxide)-block-poly(propylene oxide)-block-poly(ethylene oxide) (Pluronic F-127) in five 3D radiotherapy polymer gel dosimeters: MAGAT, PAGAT, NIPAM, VIPARnd (VIP) and VIPARCT (VIC). The current research outcomes showed that not each polymer gel dosimeter could be manufactured with Pluronic F-127. Two of the polymer gel dosimeters (PAGAT and VIP) containing the Pluronic F-127 matrix allowed for some proper dose response for radiotherapy dosimetry (a response to a dose range of e.g. 0‒50 Gy). The new best performing Pluronic-based polymer gel dosimeters were characterised by improved nuclear magnetic resonance properties, when being compared to gels with gelatine matrix at the same monomer content. These are: (i) a ~33% higher dose sensitivity; (ii) a comparable or slightly higher linear and dynamic dose range and (iii) a lower (new VIP composition, VIP3) or equivocal (new PAGAT composition, PAGAT2-Pluronic) dose threshold. However, there might be optimised gelatine based polymer dosimeters demonstrating even better sensitivity. UV-vis spectrophotometry measurements revealed that Pluronic matrices ensure six-times lower (VIP3-Pluronic) and eight-times lower (PAGAT2-Pluronic) absorbance (at 400 nm) of non-irradiated gels compared to gelatine matrices, which makes the new polymer gel dosimeters optically improved in comparison to their corresponding gelatine-based compositions. The differences in absorption reduce for higher wavelengths. Differential scanning calorimetry measurements revealed the following temperature stability ranges for the gels: (i) VIP with gelatine matrix: 0 °C‒26 °C, (ii) VIP3 with Pluronic matrix: 13.8 °C-55.2 °C, (iii) PAGAT2 with gelatine matrix: 0 °C-80 °C and (iv) PAGAT2 with Pluronic matrix: 21.4 °C-55.2 °C. In conclusion, Pluronic F-127 is an attractive co-polymer to serve as a substitute for the gelatine matrix in some 3D polymer gel dosimeters.

This work is a follow-up study for a recently-proposed 3D radiochromic gel dosimeter that contains a tetrazolium salt and a physical gel matrix made of poly(ethylene oxide)-block-poly(propylene oxide)-block-poly(ethylene oxide) (Pluronic F-127). Several tetrazolium salts were examined in this work, including tetrazolium violet, blue tetrazolium chloride, nitro blue tetrazolium chloride (NBT), tetranitro blue tetrazolium chloride (tNBT) and thiazolyl blue tetrazolium bromide (TBTB). The salt-containing gel dosimeters were compared with the first Pluronic gel composition that contained 2,3,5-triphenyltetrazolium chloride (TTC) as the radiation-sensitive component (dose sensitivity of 0.0023 (Gy cm)−1). The Pluronic gels with NBT and tNBT outperformed the other gels, including the TTC-containing gel, with respect to their dose sensitivity and low dose-response. The NBT gels were found to have better stability over time than tNBT gels. Sensitization of the gels to ionizing radiation was examined by addition of tert-butyl alcohol and sodium formate. The best composition was 0.0818% NBT (1 mM), 25% Pluronic F-127 and 0.136 × 10−2% sodium formate. This gel dosimeter was insensitive to changes in dose rate for photons of different energies. The mean dose sensitivity amounted to 0.0047 ± 0.1 × 10−4 (Gy cm)−1. A diversion in the dose-response was observed for the gel irradiated with electrons. Additional characteristics of the NBT gel were a linear-dose range and a dynamic-dose range between

This work reports results related to the manufacturing and optimisation of a leuco crystal violet (LCV)-Pluronic F-127 radiochromic gel dosimeter suitable for 3D radiotherapy dosimetry. A feature of this gel is that the natural gelatine polymer, which is most often used as a matrix in 3D dosimeters, is substituted with Pluronic F-127 synthetic copolymer (poly(ethylene oxide)-block-poly(propylene oxide)-block-poly(ethylene oxide). Pluronic F-127 ensures a higher transparency than gelatine, which may be beneficial for optical computed tomography readout, and improves the thermal properties in the temperature range above ~30 °C at which the gelatine physical gel converts to a solution. The optimal composition obtained comprises 2 mM LCV, 4 mM 4-(1,1,3,3-tetramethylbutyl)phenyl-polyethylene glycol (Triton X-100), 17 mM trichloroacetic acid (TCAA) and 25% Pluronic F-127. Its main dose-response features are 4‒150 Gy linear dose range (150 Gy was the maximal dose applied to gels in this work), 0.0070 Gy-1 cm-1 dose sensitivity (derived from absorbance (600 nm) = f (dose) for 6 MeV electrons, 0.88(3) Gy s-1 and 0.0156 Gy-1 cm-1 derived from optical density (Δµ) = f (dose) for 6 MV x-rays, 0.1010 Gy s-1), low initial colour (initial absorbance = 0.0429) and a diffusion coefficient of crystal violet (CV) in LCV-Pluronic of 0.054 ± 0.023 mm2 h-1. Raman spectroscopy was used to characterize LCV-Pluronic chemical changes after irradiation. Differential scanning calorimetry (DSC) revealed that LCV-Pluronic is stable in temperatures between approximately 11 °C and 56 °C. Irradiation of LCV-Pluronic gel impacts on its first sol-gel transition temperature and the thermal effect of this process-both increased with absorbed dose, which might be related to the degradation of Pluronic. LCV-Pluronic is a promising 3D dosimeter for ionising radiation applications. Further work is needed to improve LCV-Pluronic response in the low dose region, and characterize potential effects of pH, temperature during irradiation, and radiation quality/dose rate on dose response characteristics.

A co-polymer of poly(ethylene oxide)-block-poly(propylene oxide)-block-poly(ethylene oxide) (Pluronic F-127, PEO-PPO-PEO) was proposed as a physical gel matrix, substituting gelatine for three-dimensional polymer gel dosimeters and as a matrix for the preparation of new radiochromic gel dosimeters. Two polymer gel dosimeters and seven radiochromic gel dosimeters were obtained with this new matrix. In this review we summarise the main advantages of using Pluronic F-127 for manufacturing radiation dosimeters and the best performing new Pluronic dosimeters.

NVP-containing three-dimensional polymer gel dosimeters for radiotherapy dosimetry have been developed for more than 20 years. There have been 11 main modifications of the originally proposed VIPAR polymer gel dosimeter that altogether have amounted to 12 gel dosimeter formulae. This communication is to summarise the main chemical changes made to the VIPAR dosimeter over these years of research. The newest NVP-polymer gel dosimeters are also introduced.

This work reports on the impact of tetrakis(hydroxymethyl)phosphonium chloride (THPC) on the properties of a VIC gel dosimeter (VIC is an abbreviated acronym of VIPARCT). THPC was used as a substitute oxygen scavenger in VIC (17% N-vinylpyrrolidone, 8% N,N'-methylenebisacrylamide, 12% tert-butyl alcohol, 7.5% gelatine, 0.02% hydroquinone and an oxygen scavenger of 0.007% ascorbic acid and 0.0008% CuSO4 × 5H2O). THPC reduced the gelation time of VIC from hours to minutes. The best composition (VIC-T) contained 14 mM THPC and a reduced gelatine concentration (5%) with respect to VIC, which allowed for gelation in about 3 min. VIC-T was characterised by the same dose sensitivity (0.176 ± 0.003 Gy-1 s-1 for VIC-T and 0.171 ± 0.002 Gy-1 s-1 for VIC), dose threshold (0.5 Gy) and dynamic dose range (0.5‒50 Gy) as VIC, and a lower linear dose range (20 Gy for VIC-T, 30 Gy for VIC) (0.47 T NMR measurements). VIC-T was stable for at least 10 days after irradiation, and 3D dose distribution was stable for over 4 months after irradiation. The dose response of VIC-T was independent of the radiation dose rate, type and energy of radiation for 6 and 15 MV photons and 12 MeV electrons. This is an improvement with respect to VIC which showed a different dose response for 6 MV photons than for 12 MeV electrons and 15 MV photons. Raman spectroscopy showed similarity in the rate of radiation-induced conversion of monomers in VIC and VIC-T, indicating interaction of THPC with gelatine in VIC-T, and showed ageing of gelatine in both dosimeters. Differential scanning calorimetry showed VIC-T stability at 0 °C-80 °C (VIC: 0 °C‒29.5 °C). The chemical polymerisation and crosslinking of gelatine with THPC is reported, the mechanism of which was analysed in detail. A comparison of N-vinylpyrrolidone-containing dosimeters is presented in this work.

The new polymer gel dosimeter, based on the modification of the VIPAR gel composition, is described for the purpose of radiation dose distribution measurement in radiotherapy. It features increased concentration of the two VIPAR substrates: N-vinylpyrrolidone (8%) and gelatine (7.5%) (N,N'-methylenebisacrylamide was maintained at 4%), and the addition of copper sulphate (0.0008%) and ascorbic acid (0.007%) in order to facilitate the preparation through elimination of the need for deoxygenation of the gel. Following the exposure to ionizing radiation, polymerisation and cross-linking of the new gel monomers occurs retaining the spatial distribution of absorbed dose and causing opacity of the gel. Quantitative parameters of the new gel dose response were studied using magnetic resonance imaging to relate polymerisation induced physicochemical changes of the gel to dose. The dose threshold is found significantly lower than that of the original VIPAR gel. The linear part of measured spin-spin relaxation rate R 2 (D) (=1/T 2 (D)) reaches up to 35 Gy. Its slope and an intercept are slightly higher relative to the original VIPAR. The efficiency of the new polymer gel-magnetic resonance imaging dosimeter was also tested for dose verification of a 3D dose distribution planned by a commercially available treatment planning software (Eclipse External Beam v.6.5) and delivered by a 6 MV medical linear accelerator. The new polymer gel is proposed to be called, VIPAR nd (after VIPAR-normoxic-double).

The subject of this work is polyGeVero(®) software (GeVero Co., Poland), which has been developed to fill the requirements of fast calculations of 3D dosimetry data with the emphasis on polymer gel dosimetry for radiotherapy. This software comprises four workspaces that have been prepared for: (i) calculating calibration curves and calibration equations, (ii) storing the calibration characteristics of the 3D dosimeters, (iii) calculating 3D dose distributions in irradiated 3D dosimeters, and (iv) comparing 3D dose distributions obtained from measurements with the aid of 3D dosimeters and calculated with the aid of treatment planning systems (TPSs). The main features and functions of the software are described in this work. Moreover, the core algorithms were validated and the results are presented. The validation was performed using the data of the new PABIG(nx) polymer gel dosimeter. The polyGeVero(®) software simplifies and greatly accelerates the calculations of raw 3D dosimetry data. It is an effective tool for fast verification of TPS-generated plans for tumor irradiation when combined with a 3D dosimeter. Consequently, the software may facilitate calculations by the 3D dosimetry community. In this work, the calibration characteristics of the PABIG(nx) obtained through four calibration methods: multi vial, cross beam, depth dose, and brachytherapy, are discussed as well.

The polyGeVero® software package was elaborated for calculations of 3D dosimetry data such as the polymer gel dosimetry. It comprises four workspaces designed for: i) calculating calibrations, ii) storing calibrations in a database, iii) calculating dose distribution 3D cubes, iv) comparing two datasets e.g. a measured one with a 3D dosimetry with a calculated one with the aid of a treatment planning system. To accomplish calculations the software was equipped with a number of tools such as the brachytherapy isotopes database, brachytherapy dose versus distance calculation based on the line approximation approach, automatic spatial alignment of two 3D dose cubes for comparison purposes, 3D gamma index, 3D gamma angle, 3D dose difference, Pearson's coefficient, histograms calculations, isodoses superimposition for two datasets, and profiles calculations in any desired direction. This communication is to briefly present the main functions of the software and report on the speed of calculations performed by polyGeVero®.

Implementation of polymer gel dosimetry in radiotherapy departments calls for: easily manufactured gel dosimeters of required physical-chemical properties, set-up procedures of irradiation, adaptation of three-dimensional scanning procedures and instruments as well as fast tool for calculation of 3D absorbed dose distribution in the polymer gel dosimeters and comparison with another treatment planning system calculated dose distribution. These challenges resulted in several propositions in polymer gel dosimetry area. In this work, however, a summary of results on construction of polymer gel dosimetry software facilitating usually laborious 3D dose distributions data processing is provided.