Human Absorbed Dose Estimation of a New IN-111 Imaging Agent Based on Rat Data
Commenced in January 2007
Frequency: Monthly
Edition: International
Paper Count: 32807
Human Absorbed Dose Estimation of a New IN-111 Imaging Agent Based on Rat Data

Authors: H. Yousefnia, S. Zolghadri

Abstract:

The measurement of organ radiation exposure dose is one of the most important steps to be taken initially, for developing a new radiopharmaceutical. In this study, the dosimetric studies of a novel agent for SPECT-imaging of the bone metastasis, 111In- 1,4,7,10-tetraazacyclododecane-1,4,7,10 tetraethylene phosphonic acid (111In-DOTMP) complex, have been carried out to estimate the dose in human organs based on the data derived from rats. The radiolabeled complex was prepared with high radiochemical purity in the optimal conditions. Biodistribution studies of the complex was investigated in the male Syrian rats at selected times after injection (2, 4, 24 and 48 h). The human absorbed dose estimation of the complex was made based on data derived from the rats by the radiation absorbed dose assessment resource (RADAR) method. 111In-DOTMP complex was prepared with high radiochemical purity of >99% (ITLC). Total body effective absorbed dose for 111In- DOTMP was 0.061 mSv/MBq. This value is comparable to the other 111In clinically used complexes. The results show that the dose with respect to the critical organs is satisfactory within the acceptable range for diagnostic nuclear medicine procedures. Generally, 111In- DOTMP has interesting characteristics and can be considered as a viable agent for SPECT-imaging of the bone metastasis in the near future.

Keywords: In-111, DOTMP, Internal Dosimetry, RADAR.

Digital Object Identifier (DOI): doi.org/10.5281/zenodo.1109770

Procedia APA BibTeX Chicago EndNote Harvard JSON MLA RIS XML ISO 690 PDF Downloads 1911

References:


[1] IAEA-TECDOC-1549, “Criteria for Palliation of Bone Metastases- Clinical Applications,” Austria, Vienna: IAEA; 2007.
[2] A. Lipton, “Pathophysiology of Bone Metastases: How This Knowledge May Lead to Therapeutic Intervention,” J. Support. Oncol. vol. 2, pp. 205-20, 2004.
[3] L. D. Rybak, D. I. Rosenthal, "Radiological imaging for the diagnosis of bone metastases," Q. J. Nucl. Med., vol. 45, pp. 53-64, 2001.
[4] Z.C. Traill, D. Talbot, S. Golding, F.V. Gleeson, "Magnetic resonance imaging versus radionuclide scintigraphy in screening for bone metastases," Clin. Radiol, vol. 54, pp. 448-51, 1999.
[5] G. Zettinig, T. Leitha, B. Niederle, K. Kaserer, A. Becherer, K. Kletter. et al. “FDG positron emission tomographic, radioiodine, and MIBI imaging in a patient with poorly differentiated insular thyroid carcinoma,” Clin. Nucl. Med. Vol. 26, pp. 599–601, 2001.
[6] H. Yousefnia, A.R. Jalilian, S. Zolghadri, A. Mirzaei, A. Bahrami- Samani, M. Mirzaii, M. Ghannadi, “Development of 111In DOTMP for dosimetry of bone pain palliation agents,” J. Radioanal. Nucl. Chem. DOI 10.1007/s10967-014-3911-6.
[7] Zh. Zhou, N.K. Wagh, S.M. Ogbomo, W. Shi, Y. Jia, S.K. Brusnahan et al., "Synthesis and In Vitro and In Vivo Evaluation of Hypoxia- Enhanced 111In-Bombesin Conjugates for Prostate Cancer Imaging., J. Nucl. Med., vol. 54, pp. 1605-12, 2013.
[8] J. Lai, S.M. Quadri, P.E. Borchardt, L. Harris , R. Wucher , E. Askew et al., “Pharmaco-kinetics of radiolabeled polyclonal antiferritin in patients with Hodgkin’s disease,” Clin. Cancer Res, vol. 5, pp. 3315−23, 1999.
[9] M.W. Nijhof, W.J. Oyen, A. Van Kampen, R.A. Claessens, J.W. Van der Meer, F.H. Corstens, “Evaluation of infections of the locomotor system with indium-111-labeled human IgG scintigraphy,” J. Nucl. Med., vol. 38, pp. 1300−05, 1997.
[10] M. G. Stabin, M. Tagesson, S. R. Thomas, M. Ljungberg , S.E .Strand, “Radiation dosimetry in nuclear medicine,” Appl. Radiat. Isot., vol. 50, pp. 73-87, 1996.
[11] M. G. Stabin, “Internal Dosimetry in Nuclear Medicine,” Braz. J. Radiat. Sci., vol. 01, pp. 1-15, 2013.
[12] M.G. Stabin, J.A. Siegel, “Physical Models and Dose Factors for Use in Internal Dose Assessment,” Health. Phys., vol. 85, pp. 294-310, 2003.
[13] IAEA-TECDOC-1401, “Quantifying uncertainty in nuclear analytical measurements,” Austria, Vienna: IAEA; 2004.
[14] R. B. Sparks, B. Aydogan, “Comparison of the effectiveness of some common animal data scaling techniques in estimating human radiation dose,” Sixth International Radiopharmaceutical Dosimetry Symposium, Oak Ridge, TN: Oak Ridge Associated Universities, pp. 705–16, 1996.
[15] H. Yousefnia, S. Zolghadri, A. R. Jalilian, M. Tajik, M. Ghannadi- Maragheh, “Preliminary dosimetric evaluation of 166Ho-TTHMP for human based on biodistribution data in rats,” Appl. Radiat. Isot., vol. 94, pp. 260-5, 2014.
[16] J.J. Bevelacqua, “Internal dosimetry primer,” Radiat. Prot. Manage., vol. 22, pp. 7-17, 2005.
[17] D. J. Brenner, “Effective dose: a flawed concept that could and should be replaced,” British. J. Radiol., vol. 81, pp. 521–3, 2008.
[18] ICRP Publication 103, “The 2007 Recommendations of the International Commission on Radiological Protection,” Ann. ICRP, vol. 37, pp. 2-4, 2007.
[19] United States Pharmacopoeia 28, NF 23, pp. 1009, 2005.
[20] United States Pharmacopoeia 28, NF 23, pp. 1895, 2005.
[21] A.L. Kesner, W.A. Hsueh, J. Czernin, H. Padgett, M.E. Phelps, D.H. Silverman, “Radiation dose estimates for (18F)5-fluorouracil derived from PET-based and tissue-based methods in rats,” Mol. Imaging Biol., vol. 10, pp. 341-8, 2008.
[22] ICRP Publication 62, “Radiological Protection in Biomedical Research,” Ann. ICRP, vol. 22, pp. 3, 1993.
[23] ICRP Publication 53, “Radiation Dose to Patients from Radiopharmaceuticals,” Ann. ICRP, vol. 18, pp. 1-4, 1988.
[24] Radiation Internal Dose Information Center, “Radiation dose estimates to adults and children from various radiopharmaceuticals,” Oak Ridge Institute for Science and Education. Oak Ridge, TN 37831. Available at: orise.orau.gov/files/reacts/pedose.pdf. pp. 14, 1996.