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Pharmacokinetic Study and Bioavailability of a Novel Synthetic Trioxane Antimalarial Compound 97/63 in Rats
Author(s) -
Hari Narayan Kushwaha,
Neel Kamal Mohan,
Ashok Sharma,
Shio Kumar Singh
Publication year - 2014
Publication title -
malaria research and treatment
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.726
H-Index - 15
eISSN - 2090-8075
pISSN - 2044-4362
DOI - 10.1155/2014/759392
Subject(s) - bioavailability , pharmacokinetics , trioxane , chromatography , pharmacology , chemistry , oral administration , prodrug , high performance liquid chromatography , medicine , organic chemistry , copolymer , polymer
Single dose pharmacokinetics study of 97/63 (IND191710, 2004), a trioxane antimalarial developed by Central Drug Research Institute, Lucknow, India, was studied in rats following intravenous and oral administration. Serum samples were analysed by HPLC-UV assay. Separation was achieved on a RP-18 column attached with a guard using acetonitrile : phosphate buffer (70 : 30% v/v) with UV detector at wavelength 244 nm. Serum samples were extracted with n -hexane. Two-compartment model without lag time and first-order elimination rate was considered to be the best fit to explain the generated oral and intravenous data. Method was sensitive with limit of quantification of 10 ng mL −1 . Recovery was >74%. Terminal half-life and area under curve (AUC) after administering single oral (72 mg kg −1 ) and intravenous (18 mg kg −1 ) doses were 10.61 h, 10.57 h, and 1268.97 ng h mL −1 , 2025.75 ng h mL −1 , respectively. After oral dose, 97/63 was rapidly absorbed attaining maximum concentration 229.24 ng mL −1 at 1 h. Bioavailability of 97/63 was ~16%. The lower bioavailability of drug may be due to poor solubility and first-pass metabolism and can be improved by prodrug formation of 97/63.

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