Gao Sijia, Zhou Xuelin, Lang Liwei, Liu Honghong, Li Jianyu, Li Haotian, Wei Shizhang, Wang Dan, Xu Zhuo, Cai Huadan, Zhao Yanling, Zou Wenjun
College of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu 611137, China.
Department of Pharmacy, The Fifth Medical Center of PLA General Hospital, Beijing 100039, China.
Int J Anal Chem. 2019 Dec 9;2019:3497045. doi: 10.1155/2019/3497045. eCollection 2019.
This study aimed to develop a selective, simple, and sensitive HPLC-MS/MS method for the simultaneous determination of schisandrin and promethazine (PMZ) with its metabolite in rat plasma, which was further used for a pharmacokinetic herb-drug interaction study. HPLC-MS/MS analyses were performed on an Agilent Technologies 1290 LC and a 6410 triple quadrupole mass spectrometer. The following parameters, the lower limit of quantification (LLOQ), calibration curve, accuracy, precision, stability, matrix effect, and recovery, were validated. The linear range of the developed method for PMZ, its metabolite promethazine sulfoxide (PMZSO), and schisandrin in rat plasma was 0.5-200 ng/mL ( > 0.995), with an LLOQ of 0.5 ng/mL, which completely met the determination requirements of biosamples. The intra- and interday precision (RSD, %) was below 13.31% (below 16.67% for the LLOQ) in various plasma, whose accuracy (bias, %) was from -8.52% to 11.40%, which were both within an acceptable range. This method was successfully applied to a pharmacokinetic herb-drug interaction study after oral administration of PMZ with or without water extract. The results demonstrated that coadministration with the water extract might affect the pharmacokinetic behaviors of PMZ. In turn, when taken together with PMZ, the pharmacokinetic parameters of schisandrin, the main active component of , were also affected. The method established in the current study was selective, simple, sensitive, and widely available with good linearity, high accuracy and precision, and a stable sample preparation process. Moreover, this analytical method provides a significant approach for the investigation of herb-drug interaction between and PMZ. The potential pharmacokinetic herb-drug interaction of PMZ- and schisandrin-containing preparations should be noted.
本研究旨在建立一种选择性高、操作简便且灵敏的高效液相色谱-串联质谱(HPLC-MS/MS)方法,用于同时测定大鼠血浆中五味子醇甲和异丙嗪(PMZ)及其代谢物,该方法进一步用于药代动力学的草药-药物相互作用研究。HPLC-MS/MS分析在安捷伦科技1290液相色谱仪和6410三重四极杆质谱仪上进行。对以下参数进行了验证:定量下限(LLOQ)、校准曲线、准确度、精密度、稳定性、基质效应和回收率。所建立方法在大鼠血浆中对PMZ及其代谢物异丙嗪亚砜(PMZSO)和五味子醇甲的线性范围为0.5 - 200 ng/mL(r > 0.995),LLOQ为0.5 ng/mL,完全满足生物样品的测定要求。在不同血浆中,日内和日间精密度(RSD,%)均低于13.31%(LLOQ时低于16.67%),其准确度(偏差,%)为 - 8.52%至11.40%,均在可接受范围内。该方法成功应用于口服PMZ加或不加[具体草药]水提取物后的药代动力学草药-药物相互作用研究。结果表明,与[具体草药]水提取物合用可能会影响PMZ的药代动力学行为。反过来,当与PMZ一起服用时,[具体草药]的主要活性成分五味子醇甲的药代动力学参数也会受到影响。本研究建立的方法具有选择性、操作简便、灵敏且通用性好,线性良好、准确度和精密度高,样品制备过程稳定。此外,该分析方法为研究[具体草药]与PMZ之间的草药-药物相互作用提供了重要途径。应注意含PMZ和五味子醇甲制剂潜在的药代动力学草药-药物相互作用。