TY - JOUR
T1 - Spatial dose distributions in solid tumors from 186Re transported by liposomes using HS radiochromic media
AU - Medina, Luis A.
AU - Goins, Beth
AU - Rodríguez-Villafuerte, Mercedes
AU - Bao, Ande
AU - Martínez-Davalos, Arnulfo
AU - Awasthi, Vibhudutta
AU - Galván, Olga O.
AU - Santoyo, Cristina
AU - Phillips, William T.
AU - Brandan, María Ester
N1 - Funding Information:
Acknowledgements Luis A. Medina acknowledges the National Institute of Cancerology (Mexico) for hospitality during the development of this study, and the Instituto de Ciencias Nucleares, UNAM, for the calibration of the films. The authors would like to thank Dr. Mohan Natarajan and Xiangpeng Zheng for help with SCC-4 cell culture, Anuradha Soundararajan, Cristina Zavaleta and Maxwell Amurao for help during the image acquisition, and José-Manuel Lárraga for assistance with the Monte Carlo simulations. The authors would also like to thank Dr. Cathy Cutler at the University of Missouri Research Reactor for sponsoring our research under the Reactor Sharing Grant (US Department of Energy grant DE-FG07-02ID14380). This work was also supported in part by DGAPA-UNAM grants IN-108906 and IN-110204.
PY - 2007/7
Y1 - 2007/7
N2 - Purpose: A procedure for the measurement of spatial dose rate distribution of beta particles emitted by 186Re-liposomes in tumoral tissue, using HS GafChromic films, is presented. Methods: HNSCC xenografts were intratumorally injected with 3.7 or 11.1 MBq of 186Re-liposomes, and planar gamma camera images were acquired to determine the liposome retention in the tumor. After imaging, rats were sacrificed and tumors were excised and processed in slices; HS film sections were placed between slices and the tumor lobe was reassembled. Tumors and films were kept in the dark at 4°C for 18 h. After irradiation, films were removed and response was read using a transmission scanner. Films were analyzed to determine two-dimensional spatial dose rate distributions and cumulative dose volume histograms. Dose rate distributions were quantified using a 60Co calibration curve, the 186Re physical half-life, and a perturbation factor that takes into account the effect of the film protective layer. Results: Dose rate distributions are highly heterogeneous with maximal dose rates about 0.4 Gy h-1 in tumors injected with 3.7 MBq and 1.3 Gy h-1 in tumors injected with 11.1 MBq. Dose volume histograms showed dose distributed in more than 95% and 80% of the tumor when injected with the lower and the higher activity, respectively. Conclusion: The described procedures and techniques have shown the potential and utility of HS GafChromic film for determination of dose rate distributions in solid tumors injected intratumorally with 186Re-liposomes. The film's structure and the liposomes' biodistribution must be taken into account to obtain quantitative dose measurements.
AB - Purpose: A procedure for the measurement of spatial dose rate distribution of beta particles emitted by 186Re-liposomes in tumoral tissue, using HS GafChromic films, is presented. Methods: HNSCC xenografts were intratumorally injected with 3.7 or 11.1 MBq of 186Re-liposomes, and planar gamma camera images were acquired to determine the liposome retention in the tumor. After imaging, rats were sacrificed and tumors were excised and processed in slices; HS film sections were placed between slices and the tumor lobe was reassembled. Tumors and films were kept in the dark at 4°C for 18 h. After irradiation, films were removed and response was read using a transmission scanner. Films were analyzed to determine two-dimensional spatial dose rate distributions and cumulative dose volume histograms. Dose rate distributions were quantified using a 60Co calibration curve, the 186Re physical half-life, and a perturbation factor that takes into account the effect of the film protective layer. Results: Dose rate distributions are highly heterogeneous with maximal dose rates about 0.4 Gy h-1 in tumors injected with 3.7 MBq and 1.3 Gy h-1 in tumors injected with 11.1 MBq. Dose volume histograms showed dose distributed in more than 95% and 80% of the tumor when injected with the lower and the higher activity, respectively. Conclusion: The described procedures and techniques have shown the potential and utility of HS GafChromic film for determination of dose rate distributions in solid tumors injected intratumorally with 186Re-liposomes. The film's structure and the liposomes' biodistribution must be taken into account to obtain quantitative dose measurements.
KW - HS Gafchromic film
KW - Intratumoral dosimetry
KW - Liposomes
KW - MC simulation
KW - Radionuclide therapy
KW - Re
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U2 - 10.1007/s00259-006-0297-x
DO - 10.1007/s00259-006-0297-x
M3 - Article
C2 - 17287961
AN - SCOPUS:34250305570
SN - 1619-7070
VL - 34
SP - 1039
EP - 1049
JO - European Journal of Nuclear Medicine
JF - European Journal of Nuclear Medicine
IS - 7
ER -