Preparation and Biological Evaluation of 67Gallium- Labeled Iranian Hemiscorpius Lepturus Scorpion Venom

Author:

Jalali Amir1ORCID,Zahmatkesh Mona Haddad2ORCID,Jalilian Amir Reza3ORCID,Borujeni Amir Taheri1,Alirezapour Behrouz4

Affiliation:

1. Department of Toxicology, School of Pharmacy and Toxicology Research Center, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran

2. Department of Nuclear Pharmacy, School of Pharmacy, Guilan University of Medical Sciences, Rasht, Iran

3. Department of Nuclear Sciences and Applications, International Atomic Energy Agency, Vienna International Centre, Vienna, Austria

4. Radiation Application Research School, Nuclear Science and Technology Research Institute (NSTRI), Tehran, Iran

Abstract

Background: The Hemiscorpius lepturus (H. lepturus) is a deadly scorpion species living in the southern Iran. Objective: H. lepturus induces delayed toxicity symptoms and understanding the long term biodistribution/ biokinetic of the venom is of great interest in toxicology. Methods: A Ga-67 labeled venom was prepared using a DOTA -conjugated venom followed by radiolabeling using 67GaCl3 at 40°C for 90 min. The purification of the radiolabeled venom was performed using size exclusion-chromatography (radiochemical purity 71%). The radiolabeled venom was stable in the final solution in the presence of human serum at 37°C for 72 hours. The tissue distribution was studied in blood, heart, liver, spleen, muscle, brain, kidney, intestine and skin tissues at the intervals of 1, 4, 24, 48 and 72 hours using tissue counting and SPECT imaging. Results: The radiolabeled venom mixture obtained with an estimated molar activity of 0.52 MBq/μg. The main accumulation tissues during the first 72 hours were kidneys, blood, liver, intestines, stomach and skin, respectively. Therefore, it is likely that H. lepturus’ clinical effects and renal toxicity are primary and caused by direct effects of the H. lepturus venom. Conclusion: The results have largely shown the direct clinical effects on the studied tissues during the 72-hour period and antivenom administration can strongly alleviate the toxicity effects as early as 72 hours in the management of the patients.

Funder

Ahvaz Jundishapur University of Medical Sciences

Publisher

Bentham Science Publishers Ltd.

Subject

Pharmacology,Radiology Nuclear Medicine and imaging

Reference19 articles.

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3. Alirezapoura,B.; Jalilian, A.R.; Bolourinovin,F.; Moradkhani, S. Production and qua lity control of [67Ga]-DOTA-trastuzumab for radioimmunoscintigraphy. Iranian J. Pharmceutical Res. 2013,12(2),355-366

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