Evaluation of deoxyribonucleic acid toxicity induced by the radiopharmaceutical 99mTechnetium-Methylenediphosphonic acid and by stannous chloride in Wistar rats

Mattos, JC; Matos, VC; Rodrigues, MP; Oliveira, MB; Dantas, FJ; Santos-Filho, SD; Bernardo-Filho, M; Caldeira-De-Araujo, A

HERO ID

3491604

Reference Type

Journal Article

Year

2012

Language

English

PMID

23117436

HERO ID 3491604
In Press No
Year 2012
Title Evaluation of deoxyribonucleic acid toxicity induced by the radiopharmaceutical 99mTechnetium-Methylenediphosphonic acid and by stannous chloride in Wistar rats
Authors Mattos, JC; Matos, VC; Rodrigues, MP; Oliveira, MB; Dantas, FJ; Santos-Filho, SD; Bernardo-Filho, M; Caldeira-De-Araujo, A
Journal Molecules
Volume 17
Issue 11
Page Numbers 12974-12983
Abstract Radiopharmaceuticals are employed in patient diagnostics and disease treatments. Concerning the diagnosis aspect, technetium-99m (99mTc) is utilized to label radiopharmaceuticals for single photon computed emission tomography (SPECT) due to its physical and chemical characteristics. 99mTc fixation on pharmaceuticals depends on a reducing agent, stannous chloride (SnCl(2)) being the most widely-utilized. The genotoxic, clastogenic and anegenic properties of the 99mTc-MDP(methylene diphosphonate used for bone SPECT) and SnCl(2) were evaluated in Wistar rat blood cells using the Comet assay and micronucleus test. The experimental approach was to endovenously administer NaCl 0.9% (negative control), cyclophosphamide 50 mg/kg b.w. (positive control), SnCl(2) 500 μg/mL or 99mTc-MDP to animals and blood samples taken immediately before the injection, 3, and 24 h after (in the Comet assay) and 36 h after, for micronucleus test. The data showed that both SnCl(2) and 99mTc-MDP-induced deoxyribonucleic acid (DNA) strand breaks in rat total blood cells, suggesting genotoxic potential. The 99mTc-MDP was not able to induce a significant DNA strand breaks increase in in vivo assays. Taken together, the data presented here points to the formation of a complex between SnCl(2) in the radiopharmaceutical 99mTc-MDP, responsible for the decrease in cell damage, compared to both isolated chemical agents. These findings are important for the practice of nuclear medicine.
Doi 10.3390/molecules171112974
Pmid 23117436
Is Certified Translation No
Dupe Override No
Is Public Yes
Language Text English