作者: Lesyk Rb , Zimenkovsky Bs , Havrylyuk Dy , Kobylinska Li , Zaichenko Os
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摘要: The aim of this study was to compare the effect new synthetic 4-tiazolidinone derivatives (compounds 3882, 3288 and 3833) doxorubicin (positive control) in free form their complexes with polyethyleneglycol-containing nanoscale polymeric carrier on biochemical indicators hepatotoxicity blood serum rats. activity enzymes considered as markers hepatotoxicity, well as. concentration total protein, urea creatinine were measured It found that after injection investigated compounds activities ofalanine aminotransferase, alkaline phosphatase α-amylase increased comparison control. Doxorubicin accompanied by 4-fold increase γ-glutamyltransferase, ofcompound 3833 led 2.5-fold elevation ofthe enzyme. Complexation ofthese antineoplastic a nanocarrier lowered substantially if compared these infreeform. most evident decrease for α-amylase, γ-glutamyltransferase lactate dehydrogenase activities. normalization concentrations rats treated studied comparing introduction infreeform also detected. Thus, immobilization novel anticancer drugs possessing high general toxicity organism mitigates toxic effect, which is specific hepatodestructive effects drugs.