Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/23850
Title: 99mTc-Iabeled field bean protease inhibitor can function as an efficient tumor detecting agent
Authors: Murugesan, S
Banerji, A P
Noronha, O P D
Samuel, A M
Fernandes, A O
Issue Date: Aug-2001
Publisher: NISCAIR-CSIR, India
Abstract: Purified field bean protease inhibitor (FBPI) was labeled with 99mTcO4- to ascertain its ability to locate tumors in tumor-bearing rat models. The labeling was done with Sn2+ as a reducing agent and the yield was 95%. It was stable for 2 hr at ambient temperature. The biodistribution study of the intravenously injected radiolabeled FBPI in normal Wistar rats at various time intervals showed a rapid blood clearance from the systemic circulation (~5hr). The complex was predominantly excreted through the renal and the hepatobiliary systems. In vivo distribution and scintiimaging of 99mTc-FBPI were carried out in rats bearing carcinogen-induced mammary tumor or transplanted C6-gliomas. The results obtained were compared with conventional tumor-seeking radiopharmaceuticals such as 99mTc-(V)dimercaptosuccinic acid (DMSA), 201Thallous chloride (TICI) and 9mTc-Citrate. The tumor to muscle (T/M) ratios obtained with 99mTc-FBPI in rat C6 glioma was nearly 2 to 5-fold higher than obtained with all the three conventional tumor-seeking agents. The T/M ratio obtained with 99mTc-FBPI in rat mammary tumor on the other hand appeared to be 2-3-fold higher than noted with 99mTc(V)-DMSA and 201TICI. The ratio was however comparable with that obtained with 99mTc-Citrate. The study indicated that 999mTc -FBPI has the specific potentials for imaging gliomas and possibly other tumors as well.
Page(s): 742-747
ISSN: 0975-1009 (Online); 0019-5189 (Print)
Appears in Collections:IJEB Vol.39(08) [August 2001]

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