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Dive into the research topics where Tina Gorjiara is active.

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Featured researches published by Tina Gorjiara.


Medical Physics | 2011

Investigation of radiological properties and water equivalency of PRESAGE ® dosimeters

Tina Gorjiara; Robin Hill; Zdenka Kuncic; J Adamovics; Stephen Bosi; Jung-Ha Kim; Clive Baldock

PURPOSE PRESAGE is a dosimeter made of polyurethane, which is suitable for 3D dosimetry in modern radiation treatment techniques. Since an ideal dosimeter is radiologically water equivalent, the authors investigated water equivalency and the radiological properties of three different PRESAGE formulations that differ primarily in their elemental compositions. Two of the formulations are new and have lower halogen content than the original formulation. METHODS The radiological water equivalence was assessed by comparing the densities, interaction probabilities, and radiation dosimetry properties of the three different PRESAGE formulations to the corresponding values for water. The relative depth doses were calculated using Monte Carlo methods for 50, 100, 200, and 350 kVp and 6 MV x-ray beams. RESULTS The mass densities of the three PRESAGE formulations varied from 5.3% higher than that of water to as much as 10% higher than that of water for the original formulation. The probability of photoelectric absorption in the three different PRESAGE formulations varied from 2.2 times greater than that of water for the new formulations to 3.5 times greater than that of water for the original formulation. The mass attenuation coefficient for the three formulations is 12%-50% higher than the value for water. These differences occur over an energy range (10-100 keV) in which the photoelectric effect is the dominant interaction. The collision mass stopping powers of the relatively lower halogen-containing PRESAGE formulations also exhibit marginally better water equivalency than the original higher halogen-containing PRESAGE formulation. Furthermore, the depth dose curves for the lower halogen-containing PRESAGE formulations are slightly closer to that of water for a 6 MV beam. In the kilovoltage energy range, the depth dose curves for the lower halogen-containing PRESAGE formulations are in better agreement with water than the original PRESAGE formulation. CONCLUSIONS Based on the results of this study, the new PRESAGE formulations with lower halogen content are more radiologically water equivalent overall than the original formulation. This indicates that the new PRESAGE formulations are better suited to clinical applications and are more accurate dosimeters and phantoms than the original PRESAGE formulation. While correction factors are still needed to convert the dose measured by the dosimeter to an absorbed dose in water in the kilovoltage energy range, these correction factors are considerably smaller for the new PRESAGE formulations compared to the original PRESAGE and the existing polymer gel dosimeters.


Physics in Medicine and Biology | 2011

Radiological characterization and water equivalency of genipin gel for x-ray and electron beam dosimetry.

Tina Gorjiara; Robin Hill; Zdenka Kuncic; Stephen Bosi; J.B. Davies; Clive Baldock

The genipin radiochromic gel offers enormous potential as a three-dimensional dosimeter in advanced radiotherapy techniques. We have used several methods (including Monte Carlo simulation), to investigate the water equivalency of genipin gel by characterizing its radiological properties, including mass and electron densities, photon interaction cross sections, mass energy absorption coefficient, effective atomic number, collisional, radiative and total mass stopping powers and electron mass scattering power. Depth doses were also calculated for clinical kilovoltage and megavoltage x-ray beams as well as megavoltage electron beams. The mass density, electron density and effective atomic number of genipin were found to differ from water by less than 2%. For energies below 150 keV, photoelectric absorption cross sections are more than 3% higher than water due to the strong dependence on atomic number. Compton scattering and pair production interaction cross sections for genipin gel differ from water by less than 1%. The mass energy absorption coefficient is approximately 3% higher than water for energies <60 keV due to the dominance of photoelectric absorption in this energy range. The electron mass stopping power and mass scattering power differ from water by approximately 0.3%. X-ray depth dose curves for genipin gel agree to within 1% with those for water. Our results demonstrate that genipin gel can be considered water equivalent for kilovoltage and megavoltage x-ray beam dosimetry. For megavoltage electron beam dosimetry, however, our results suggest that a correction factor may be needed to convert measured dose in genipin gel to that of water, since differences in some radiological properties of up to 3% compared to water are observed. Our results indicate that genipin gel exhibits greater water equivalency than polymer gels and PRESAGE formulations.


Medical Physics | 2012

Water and tissue equivalence of a new PRESAGE® formulation for 3D proton beam dosimetry : a Monte Carlo study

Tina Gorjiara; Zdenka Kuncic; Simon J. Doran; J Adamovics; Clive Baldock

PURPOSE To evaluate the water and tissue equivalence of a new PRESAGE(®) 3D dosimeter for proton therapy. METHODS The GEANT4 software toolkit was used to calculate and compare total dose delivered by a proton beam with mean energy 62 MeV in a PRESAGE(®) dosimeter, water, and soft tissue. The dose delivered by primary protons and secondary particles was calculated. Depth-dose profiles and isodose contours of deposited energy were compared for the materials of interest. RESULTS The proton beam range was found to be ≈27 mm for PRESAGE(®), 29.9 mm for soft tissue, and 30.5 mm for water. This can be attributed to the lower collisional stopping power of water compared to soft tissue and PRESAGE(®). The difference between total dose delivered in PRESAGE(®) and total dose delivered in water or tissue is less than 2% across the entire water∕tissue equivalent range of the proton beam. The largest difference between total dose in PRESAGE(®) and total dose in water is 1.4%, while for soft tissue it is 1.8%. In both cases, this occurs at the distal end of the beam. Nevertheless, the authors find that PRESAGE(®) dosimeter is overall more tissue-equivalent than water-equivalent before the Bragg peak. After the Bragg peak, the differences in the depth doses are found to be due to differences in primary proton energy deposition; PRESAGE(®) and soft tissue stop protons more rapidly than water. The dose delivered by secondary electrons in the PRESAGE(®) differs by less than 1% from that in soft tissue and water. The contribution of secondary particles to the total dose is less than 4% for electrons and ≈1% for protons in all the materials of interest. CONCLUSIONS These results demonstrate that the new PRESAGE(®) formula may be considered both a tissue- and water-equivalent 3D dosimeter for a 62 MeV proton beam. The results further suggest that tissue-equivalent thickness may provide better dosimetric and geometric accuracy than water-equivalent thickness for 3D dosimetry of this proton beam.


6th International Conference on 3D Radiation Dosimetry, IC3DDose 2010 | 2010

Study of dosimetric water equivalency of PRESAGE® for megavoltage and kilovoltage x-ray beams

Tina Gorjiara; Robin Hill; Jung-Ha Kim; Zdenka Kuncic; J Adamovics; Clive Baldock

PRESAGE is a dosimeter that is suitable for 3D dosimetry. To be used as an ideal dosimeter, however, it should present radiologically water equivalent properties. In this work, we have investigated the radiological properties of three different PRESAGE® formulations. The radiological water equivalence was assessed by comparing the photon cross sections and radiation dosimetry properties of the three different PRESAGE® formulations with the corresponding values for water. Relative depth doses were calculated using Monte Carlo methods for 75, 125, 180 and 280 kVp and 6 MV x-ray beams. Based on the results of this study, the PRESAGE® formulations with lower halogen content are more dosimetrically water equivalent.


Medical Physics | 2012

Water and tissue equivalence of a new PRESAGE{sup Registered-Sign} formulation for 3D proton beam dosimetry: A Monte Carlo study

Tina Gorjiara; Zdenka Kuncic; Simon J. Doran; J Adamovics

PURPOSE To evaluate the water and tissue equivalence of a new PRESAGE(®) 3D dosimeter for proton therapy. METHODS The GEANT4 software toolkit was used to calculate and compare total dose delivered by a proton beam with mean energy 62 MeV in a PRESAGE(®) dosimeter, water, and soft tissue. The dose delivered by primary protons and secondary particles was calculated. Depth-dose profiles and isodose contours of deposited energy were compared for the materials of interest. RESULTS The proton beam range was found to be ≈27 mm for PRESAGE(®), 29.9 mm for soft tissue, and 30.5 mm for water. This can be attributed to the lower collisional stopping power of water compared to soft tissue and PRESAGE(®). The difference between total dose delivered in PRESAGE(®) and total dose delivered in water or tissue is less than 2% across the entire water∕tissue equivalent range of the proton beam. The largest difference between total dose in PRESAGE(®) and total dose in water is 1.4%, while for soft tissue it is 1.8%. In both cases, this occurs at the distal end of the beam. Nevertheless, the authors find that PRESAGE(®) dosimeter is overall more tissue-equivalent than water-equivalent before the Bragg peak. After the Bragg peak, the differences in the depth doses are found to be due to differences in primary proton energy deposition; PRESAGE(®) and soft tissue stop protons more rapidly than water. The dose delivered by secondary electrons in the PRESAGE(®) differs by less than 1% from that in soft tissue and water. The contribution of secondary particles to the total dose is less than 4% for electrons and ≈1% for protons in all the materials of interest. CONCLUSIONS These results demonstrate that the new PRESAGE(®) formula may be considered both a tissue- and water-equivalent 3D dosimeter for a 62 MeV proton beam. The results further suggest that tissue-equivalent thickness may provide better dosimetric and geometric accuracy than water-equivalent thickness for 3D dosimetry of this proton beam.


6th International Conference on 3D Radiation Dosimetry (IC3DDose 2010) | 2010

Water equivalency evaluation of PRESAGE® dosimeters for dosimetry of Cs-137 and Ir-192 brachytherapy sources

Tina Gorjiara; Robin Hill; Zdenka Kuncic; Clive Baldock

A major challenge in brachytherapy dosimetry is the measurement of steep dose gradients. This can be achieved with a high spatial resolution three dimensional (3D) dosimeter. PRESAGE® is a polyurethane based dosimeter which is suitable for 3D dosimetry. Since an ideal dosimeter is radiologically water equivalent, we have investigated the relative dose response of three different PRESAGE® formulations, two with a lower chloride and bromide content than original one, for Cs-137 and Ir-192 brachytherapy sources. Doses were calculated using the EGSnrc Monte Carlo package. Our results indicate that PRESAGE® dosimeters are suitable for relative dose measurement of Cs-137 and Ir-192 brachytherapy sources and the lower halogen content PRESAGE® dosimeters are more water equivalent than the original formulation.


Physics in Medicine and Biology | 2015

Issues involved in the quantitative 3D imaging of proton doses using optical CT and chemical dosimeters

Simon J. Doran; Tina Gorjiara; Andrzej Kacperek; J Adamovics; Zdenka Kuncic; Clive Baldock

Abstract Dosimetry of proton beams using 3D imaging of chemical dosimeters is complicated by a variation with proton linear energy transfer (LET) of the dose–response (the so-called ‘quenching effect’). Simple theoretical arguments lead to the conclusion that the total absorbed dose from multiple irradiations with different LETs cannot be uniquely determined from post-irradiation imaging measurements on the dosimeter. Thus, a direct inversion of the imaging data is not possible and the proposition is made to use a forward model based on appropriate output from a planning system to predict the 3D response of the dosimeter. In addition to the quenching effect, it is well known that chemical dosimeters have a non-linear response at high doses. To the best of our knowledge it has not yet been determined how this phenomenon is affected by LET. The implications for dosimetry of a number of potential scenarios are examined. Dosimeter response as a function of depth (and hence LET) was measured for four samples of the radiochromic plastic PRESAGE®, using an optical computed tomography readout and entrance doses of 2.0 Gy, 4.0 Gy, 7.8 Gy and 14.7 Gy, respectively. The dosimeter response was separated into two components, a single-exponential low-LET response and a LET-dependent quenching. For the particular formulation of PRESAGE® used, deviations from linearity of the dosimeter response became significant for doses above approximately 16 Gy. In a second experiment, three samples were each irradiated with two separate beams of 4 Gy in various different configurations. On the basis of the previous characterizations, two different models were tested for the calculation of the combined quenching effect from two contributions with different LETs. It was concluded that a linear superposition model with separate calculation of the quenching for each irradiation did not match the measured result where two beams overlapped. A second model, which used the concept of an ‘effective dose’ matched the experimental results more closely. An attempt was made to measure directly the quench function for two proton beams as a function of all four variables of interest (two physical doses and two LET values). However, this approach was not successful because of limitations in the response of the scanner.


6th International Conference on 3D Radiation Dosimetry, IC3DDose 2010 | 2010

An evaluation of Genipin gel as a water equivalent dosimeter for megavoltage electron beams and kilovoltage x-ray beams

Tina Gorjiara; Robin Hill; Zdenka Kuncic; Stephen Bosi; Clive Baldock

Genipin gel is a radiochromic gel with the potential to be used as a three dimensional (3D) dosimeter. An ideal dosimeter should present radiologically water equivalent properties. In this work, we have evaluated the water equivalency of genipin gel by calculating its radiological properties, such as mass and electron density, effective atomic number, fractional interaction probabilities, mass energy absorption coefficient and mass stopping powers as well as depth doses for kilovoltage x-ray and megavoltage electron beams. Based on the results of this study, we conclude that genipin gel is a water equivalent dosimeter.


7th International Conference on 3D Radiation Dosimetry (IC3DDose) | 2015

The quenching effect in PRESAGE® dosimetry of proton beams: Is an empirical correction feasible?

Simon J. Doran; Tina Gorjiara; J Adamovics; Zdenka Kuncic; Andrzej Kacperek; Clive Baldock

Chemical dosimeters, including PRESAGE® as used in optical CT, exhibit significant quenching effects in response to proton irradiation and this may limit their widespread uptake. This study performs careful measurements of the observed quenching of a recently developed variant of PRESAGE® in a 60 MeV proton beam and uses them to attempt an empirical correction of a simple superposition of two unmodulated beams.


7th International Conference on 3D Radiation Dosimetry (IC3DDose) | 2013

Monte Carlo water-equivalence study of two PRESAGE® formulations for proton beam dosimetry

Tina Gorjiara; Zdenka Kuncic; J Adamovics; Clive Baldock

PRESAGE® is a radiochromic solid dosimeter which shows promising potential for 3D proton beam dosimetry. Since an idea dosimeter should be water-equivalent, total depth dose distributions in two PRESAGE® formulations irradiated by a 62 MeV proton beam were compared with that in water using GEANT4 Monte Carlo simulations. The dose delivered by secondary particles was also calculated. Our results show that after water-equivalent depth scaling, PRESAGE® can be considered water equivalent for dosimetry of a 62 MeV clinical proton beam.

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Andrzej Kacperek

Clatterbridge Cancer Centre NHS Foundation Trust

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B Healy

Princess Alexandra Hospital

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Brendan Hill

Queensland University of Technology

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