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首页> 外文期刊>Journal of Chromatographic Science >Determination and Pharmacokinetic Study of Pirfenidone in Rat Serum by High-Performance Thin-Layer Chromatography
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Determination and Pharmacokinetic Study of Pirfenidone in Rat Serum by High-Performance Thin-Layer Chromatography

机译:高效薄层色谱法测定大鼠血清中吡非尼酮的药动学

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摘要

A rapid, sensitive and selective high-performance thin-layer chromatography (HPTLC) method was developed and validated for the determination and pharmacokinetics of pirfenidone in rat serum. One-step protein precipitation by methanol is reported, and serum samples were separated by HPTLC using a simple mobile phase of toluene-methanol in the ratio of 8:2. The retardation factor of pirfenidone in the serum sample was 0.45 with the detection performed at 315 nm. The calibration curve was linear over the range of 100-1,200 ng/spot with a lower limit of quantitation of 40 ng/spot. The mean recovery of pirfenidone in serum was in the range of 70.6-75.8%, and intra-day and inter-day precision were both <14.1%. This method was successfully applied to the pharmacokinetic study of pirfenidone in rats on oral administration of the drug at a dose of 15.0 mg/kg.
机译:建立了一种快速,灵敏和选择性的高性能薄层色谱法(HPTLC),并已用于大鼠血清中吡非尼酮的测定和药代动力学验证。据报道,甲醇会一步沉淀蛋白质,使用简单的甲苯-甲醇流动相(比率为8:2)通过HPTLC分离血清样品。血清样品中吡非尼酮的阻滞因子为0.45,检测波长为315 nm。校准曲线在100-1,200 ng / spot范围内呈线性,定量下限为40 ng / spot。血清中吡非尼酮的平均回收率在70.6-75.8%范围内,日内和日间精度均<14.1%。该方法已成功应用于吡非尼酮以15.0 mg / kg的口服剂量在大鼠体内进行药代动力学研究。

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