132. Study of the dosimetric robustness of PVA-GTA based Fricke gels against manufacture parameters. (December 2018)
- Record Type:
- Journal Article
- Title:
- 132. Study of the dosimetric robustness of PVA-GTA based Fricke gels against manufacture parameters. (December 2018)
- Main Title:
- 132. Study of the dosimetric robustness of PVA-GTA based Fricke gels against manufacture parameters
- Authors:
- Gallo, S.
Gambarini, G.
Ianni, L.
Veronese, I. - Abstract:
- Abstract: Purpose: Fricke gel dosimeters (FGDs) based on poly-vinyl alcohol (PVA) as gelling agent and glutaraldehyde (GTA) as cross-linker, were developed with the aim to overcome the drawbacks affecting the FGDs prepared with traditional natural gel matrices like gelatin or agarose[1] . Here, we investigate the dosimetric robustness of PVA-GTA FGDs against parameters influencing their preparation, like pH and temperature of gelling. Materials and Methods: PVA-GTA matrices undergo gelling by heating instead of cooling. Gelling temperatures from 6 °C to 40 °C were considered. FGDs with PVA and GTA concentrations of 10% w/w and 1% w/w respectively, were arranged preparing Fricke solutions with different amounts of sulfuric acid in the interval 18–100 mM. FGDs in spectrophotometry cuvettes (10 mm optical path) were uniformly irradiated with a 137Cs source. The optical absorbance (OA) properties and dose-response in the interval 0–35 Gy were investigated. Furthermore, FGDs in form of thin layers (3 mm optical path, area 10 × 5 cm 2 ) were irradiated with 80 kV X-rays producing a steep dose gradient. Light transmittance images were acquired before irradiation and at consecutive times up to 6 h post-irradiation to derive the Fe3+ diffusion coefficient. Results: OA spectra and dose-response curves of FGDs were independent of the gelling temperature. A sensitivity of approximately 0.073 Gy-1 was obtained. By contrast, as in traditional FGDs, sulfuric acid concentrationAbstract: Purpose: Fricke gel dosimeters (FGDs) based on poly-vinyl alcohol (PVA) as gelling agent and glutaraldehyde (GTA) as cross-linker, were developed with the aim to overcome the drawbacks affecting the FGDs prepared with traditional natural gel matrices like gelatin or agarose[1] . Here, we investigate the dosimetric robustness of PVA-GTA FGDs against parameters influencing their preparation, like pH and temperature of gelling. Materials and Methods: PVA-GTA matrices undergo gelling by heating instead of cooling. Gelling temperatures from 6 °C to 40 °C were considered. FGDs with PVA and GTA concentrations of 10% w/w and 1% w/w respectively, were arranged preparing Fricke solutions with different amounts of sulfuric acid in the interval 18–100 mM. FGDs in spectrophotometry cuvettes (10 mm optical path) were uniformly irradiated with a 137Cs source. The optical absorbance (OA) properties and dose-response in the interval 0–35 Gy were investigated. Furthermore, FGDs in form of thin layers (3 mm optical path, area 10 × 5 cm 2 ) were irradiated with 80 kV X-rays producing a steep dose gradient. Light transmittance images were acquired before irradiation and at consecutive times up to 6 h post-irradiation to derive the Fe3+ diffusion coefficient. Results: OA spectra and dose-response curves of FGDs were independent of the gelling temperature. A sensitivity of approximately 0.073 Gy-1 was obtained. By contrast, as in traditional FGDs, sulfuric acid concentration significantly affected the OA spectra as well as the sensitivity and linearity of the PVA-GTA FGDs. Both gelling temperature gradient and pH did not influence the Fe3+ diffusion coefficient, assessed equal to approximately 0.22 mm 2 /h, i.e. more than two times lower than in traditional FGDs. Conclusions: The robustness of PVA-GTA-FGDs against preparation parameters represent a significant advantage over traditional FGDs. In particular, the response independence of the gelling temperature may enable the manufacture of large FGD phantoms without any gradient in sensitivity. … (more)
- Is Part Of:
- Physica medica. Volume 56(2018)Supplement 2
- Journal:
- Physica medica
- Issue:
- Volume 56(2018)Supplement 2
- Issue Display:
- Volume 56, Issue 2 (2018)
- Year:
- 2018
- Volume:
- 56
- Issue:
- 2
- Issue Sort Value:
- 2018-0056-0002-0000
- Page Start:
- 146
- Page End:
- 147
- Publication Date:
- 2018-12
- Subjects:
- Medical physics -- Periodicals
Biophysics -- Periodicals
Biophysics -- Periodicals
Imagerie médicale -- Périodiques
Radiothérapie -- Périodiques
Rayons X -- Sécurité -- Mesures -- Périodiques
Physique -- Périodiques
Médecine -- Périodiques
610.153 - Journal URLs:
- http://www.sciencedirect.com/science/journal/11201797 ↗
http://www.clinicalkey.com/dura/browse/journalIssue/11201797 ↗
http://www.clinicalkey.com.au/dura/browse/journalIssue/11201797 ↗
http://www.elsevier.com/journals ↗
http://www.physicamedica.com ↗ - DOI:
- 10.1016/j.ejmp.2018.04.143 ↗
- Languages:
- English
- ISSNs:
- 1120-1797
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6475.070000
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