Dai Tingting, Sun Guoxiang
School of Pharmacy, Shenyang Pharmaceutical University, Shenyang, 110032, Liaoning, China.
Anal Bioanal Chem. 2022 May;414(13):3927-3943. doi: 10.1007/s00216-022-04037-z. Epub 2022 Apr 9.
Zhenju Antihypertensive Tablet is one of the Flos Chrysanthemi Indici preparations (FCIP) with antihypertensive effect. In order to investigate its process in vivo, a method using ultra-high performance liquid chromatography coupled with quadruple Exactive mass spectrometry (UHPLC-Q-Exactive-MS) was established for comprehensive analysis of the absorbed active component and metabolites in rat plasma, urine, and feces after the oral administration of FCIP. As a result, a total of 61 FCIP-related xenobiotics were identified, including 35 in plasma (25 prototypes, 10 metabolites), 40 in urine (23 prototypes, 17 metabolites), and 25 in feces (12 prototypes, 13 metabolites). The metabolism reactions included phase I reactions (such as oxidation, methylation, and reduction) and phase II reactions (such as sulfate conjugation and glucuronide conjugation). Meanwhile, a verified and optimized ultra-performance liquid chromatography with triple quadrupole mass spectrometry (UHPLC-QQQ-MS/MS) method was developed for the simultaneous investigation of the pharmacokinetic profiles of four markers in FCIP. The results showed that all of the four components had good oral absorption effect. This study simultaneously investigated the comprehensive metabolic profiling of FCIP in rat plasma, urine, and feces after the oral administration as well as the four components pharmacokinetic behavior. The results can provide the therapeutic material basis for FCIP.
珍菊降压片是具有降压作用的野菊花制剂之一。为了研究其体内过程,建立了一种超高效液相色谱-四极杆Exactive质谱联用(UHPLC-Q-Exactive-MS)方法,用于口服野菊花制剂后大鼠血浆、尿液和粪便中吸收的活性成分及代谢产物的全面分析。结果共鉴定出61种与野菊花制剂相关的外源性物质,其中血浆中35种(25种原型药、10种代谢产物),尿液中40种(23种原型药、17种代谢产物),粪便中25种(12种原型药、13种代谢产物)。代谢反应包括I相反应(如氧化、甲基化和还原)和II相反应(如硫酸酯结合和葡萄糖醛酸结合)。同时,建立了一种经验证和优化的超高效液相色谱-三重四极杆质谱联用(UHPLC-QQQ-MS/MS)方法,用于同时研究野菊花制剂中4种标志物的药代动力学特征。结果表明,4种成分均具有良好的口服吸收效果。本研究同时考察了口服给药后野菊花制剂在大鼠血浆、尿液和粪便中的综合代谢谱以及4种成分的药代动力学行为。研究结果可为野菊花制剂提供治疗物质基础。