...
首页> 外文期刊>Planta medica: Natural products and medicinal plant research >Pharmacokinetic study of borneol and menthol in rats after oral administration of qingyan drop pills.
【24h】

Pharmacokinetic study of borneol and menthol in rats after oral administration of qingyan drop pills.

机译:青岩滴丸口服后冰片和薄荷醇在大鼠体内的药代动力学研究。

获取原文
获取原文并翻译 | 示例
           

摘要

Both borneol and menthol are bioactive substances derived from Chinese herbal medicines. In order to understand the pharmacokinetics of borneol and menthol in Qingyan drop pills, a rapid, sensitive, and simple gas chromatographic (GC) method with flame ionization detection (FID) was developed for the simultaneous determination of borneol and menthol in rat plasma. Sample preparations were carried out by liquid-liquid extraction (LLE) with an internal standard solution of naphthalene. The analytes and internal standard (IS, naphthalene) were separated well on an HP-1 capillary column. The pharmacokinetic parameters were estimated by a compartmental method using the Phoenix WinNonlin software program (Version 6.0). The standard curves were linear over a wide concentration range of 2.5-50.0 ng/microL ( R = 0.9963), 8.7-62.2 ng/microL ( R = 0.9994) for both borneol and menthol in plasma, respectively. The limits of quantification (LOQ) of borneol and menthol in plasma were 2.4 ng/microL and 5.0 ng/microL, respectively. The intra-day precisions for borneol and menthol were < or = 10.0 % R. S. D. at the LOQ and < or = 6.0 % at higher concentrations. The average value of CMAX was 18.97 +/- 2.71 ng/microL with a TMAX at 20.00 +/- 0.00 min for borneol after oral administration of the drop pills; for menthol, the average value of CMAX was 79.02 +/- 11.40 ng/microL with a TMAX at 25.00 +/- 4.40 min. This validated assay method was successfully applied to a pharmacokinetic study of borneol and menthol after oral administration of Qingyan drop pills in rat. The results showed that the kinetics of borneol and menthol can be described by an open one-compartment model. The pharmacokinetic parameters provide some information for clinical administration of Qingyan drop pills.
机译:冰片和薄荷醇都是源自中草药的生物活性物质。为了了解冰片和薄荷醇在青岩滴丸中的药代动力学,开发了一种快速,灵敏,简单的气相色谱(GC)火焰火焰电离检测(FID)方法,用于同时测定大鼠血浆中的冰片和薄荷醇。样品制备是通过萘的内标液通过液-液萃取(LLE)进行的。分析物和内标物(IS,萘)在HP-1毛细管柱上分离良好。使用Phoenix WinNonlin软件程序(6.0版)通过隔室方法估计药代动力学参数。对于血浆中的冰片和薄荷醇,标准曲线在2.5-50.0 ng / microL(R = 0.9963),8.7-62.2 ng / microL(R = 0.9994)的宽浓度范围内均呈线性。血浆中冰片和薄荷醇的定量限(LOQ)分别为2.4 ng / microL和5.0 ng / microL。冰片和薄荷醇的日内精确度在LOQ时为R. S. D.≤10.0%,在较高浓度时为<或= 6.0%。口服滴丸后的冰片的CMAX平均值为18.97 +/- 2.71 ng / microL,TMAX为20.00 +/- 0.00 min;对于薄荷醇,CMAX的平均值为79.02 +/- 11.40 ng / microL,TMAX值为25.00 +/- 4.40 min。该验证的测定方法已成功应用于大鼠口服清咽滴丸后冰片和薄荷醇的药代动力学研究。结果表明,冰片和薄荷醇的动力学可以用开放的一室模型描述。药代动力学参数为青岩滴丸的临床给药提供了一些信息。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号