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新型合成三恶烷抗疟化合物97/63在大鼠体内的药代动力学研究及生物利用度

Pharmacokinetic study and bioavailability of a novel synthetic trioxane antimalarial compound 97/63 in rats.

作者信息

Kushwaha Hari Narayan, Mohan Neel Kamal, Sharma Ashok Kumar, Singh Shio Kumar

机构信息

Pharmacokinetics and Metabolism Division, CSIR-Central Drug Research Institute, Lucknow 226001, India.

Medicinal and Process Chemistry Division, CSIR-Central Drug Research Institute, Lucknow 226001, India.

出版信息

Malar Res Treat. 2014;2014:759392. doi: 10.1155/2014/759392. Epub 2014 Sep 11.

Abstract

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.

摘要

印度勒克瑙中央药物研究所研发的三恶烷抗疟药97/63(IND191710,2004)在大鼠体内进行了静脉注射和口服给药后的单剂量药代动力学研究。血清样本通过高效液相色谱-紫外检测法进行分析。在配备保护柱的反相-18柱上,使用乙腈∶磷酸盐缓冲液(70∶30% v/v)进行分离,紫外检测器波长设定为244 nm。血清样本用正己烷萃取。无滞后时间和一级消除速率的二室模型被认为最能拟合所生成的口服和静脉给药数据。该方法灵敏度高,定量限为10 ng mL⁻¹。回收率>74%。单次口服(72 mg kg⁻¹)和静脉注射(18 mg kg⁻¹)剂量后的末端半衰期和曲线下面积(AUC)分别为10.61 h、10.57 h和1268.97 ng h mL⁻¹、2025.75 ng h mL⁻¹。口服给药后,97/63迅速吸收,1小时时达到最大浓度229.24 ng mL⁻¹。97/63的生物利用度约为16%。药物生物利用度较低可能是由于溶解度差和首过代谢,可通过97/63的前药形成来改善。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73d5/4180634/4c151598451d/MRT2014-759392.001.jpg

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