Hao Haiping, Wang Guangji, Li Peng, Li Jing, Ding Zuoqi
Key Laboratory of Drug Metabolism and Pharmacokinetics E04#, China Pharmaceutical University, 1 Shennong Road, Nanjing 210038, China.
J Pharm Biomed Anal. 2006 Feb 13;40(2):382-8. doi: 10.1016/j.jpba.2005.07.029. Epub 2005 Sep 19.
A rapid and sensitive method for the simultaneous determination of cryptotanshinone and its active metabolite tanshinone IIA in rat plasma was developed and well validated, using high-performance liquid chromatographic separation with tandem mass spectrometric detection. This method entailed a single step of liquid-liquid extraction with ethyl acetate from a small volume of plasmas. The analytes and internal standard diazepam were baseline separated on a Shim-pack VP-ODS analytical column. Detection was performed on a triple quadrupole tandem mass spectrometer equipped with electrospray ionization source operated under selected reaction monitoring (SRM) mode. The method was linear in the concentration range of 1-100 ng/ml for both tanshinone IIA and cryptotanshinone. The intra- and inter-day precisions (R.S.D.%) were within 10.2% for both analytes. Deviation of the assay accuracies was within +/-12.0% for both analytes. Both analytes were proved to be stable during all sample storing, preparation and analytic procedures. The method was successfully applied to a pharmacokinetic study after an oral administration of cryptotanshinone to rats with a dose of 20 mg/kg. With the lower limits of quantification at 1.0 ng/ml for tanshinone IIA and 0.2 ng/ml for cryptotanshinone, this method was proved to be sensitive enough and reproducible for the pharmacokinetics study of both tanshinones.
建立了一种快速灵敏的同时测定大鼠血浆中隐丹参酮及其活性代谢物丹参酮ⅡA的方法,并进行了充分验证,该方法采用高效液相色谱分离-串联质谱检测。此方法只需用乙酸乙酯从少量血浆中进行一步液-液萃取。分析物和内标地西泮在Shim-pack VP-ODS分析柱上实现基线分离。检测在配备电喷雾电离源的三重四极杆串联质谱仪上进行,采用选择反应监测(SRM)模式。该方法对丹参酮ⅡA和隐丹参酮在1-100 ng/ml浓度范围内呈线性。两种分析物的日内和日间精密度(相对标准偏差,R.S.D.%)均在10.2%以内。两种分析物的测定准确度偏差均在±12.0%以内。两种分析物在所有样品储存、制备和分析过程中均被证明是稳定的。该方法成功应用于给大鼠口服20 mg/kg剂量隐丹参酮后的药代动力学研究。由于丹参酮ⅡA的定量下限为1.0 ng/ml,隐丹参酮的定量下限为0.2 ng/ml,该方法被证明对两种丹参酮的药代动力学研究足够灵敏且可重复。