Gong Leilei, Xu Haiyu, Yuan Huijun, Wang Lan, Yin Xiaojie, Fan Moqi, Cheng Long, Ma Xiaojing, Liang Rixin, Yang Hongjun
Institute of Chinese Materia Medica, China Academy of Chinese Medical Science No. 16 Nanxiaojie, Dongzhimennei Ave. Beijing 100700 P. R. China
School of Traditional Chinese Medicine, Capital Medical University Beijing 100069 P. R. China.
RSC Adv. 2018 Apr 26;8(28):15725-15739. doi: 10.1039/c7ra12659j. eCollection 2018 Apr 23.
Yindanxinnaotong capsule (YDXNT), a traditional Chinese formula, has been used to treat cardio-cerebrovascular diseases for several decades. Previous research has focused on evaluating the pharmacological properties and main compounds of YDXNT and . However, the multiple bioactive compounds remain poorly understood. In the present research, an integrative strategy using UPLC-Q-TOF-MS combined with UPLC-QqQ-MS was employed to detect the absorbed constituents and investigate the pharmacokinetics of main compounds in the plasma after oral administration of YDXNT. UPLC-Q-TOF-MS was developed to detect the absorbed constituents and their metabolites in the plasma after oral administration in rats. A total of 52 constituents, including 44 prototype compounds and 8 metabolites, were identified or tentatively characterized. Then, nine main compounds (quercetin, isorhamnetin, kaempferol, ginkgolide A, ginkgolide B, ginkgolide C, bilobalide, tanshinone IIA, and salvianolic acid B) were chosen to further investigate the pharmacokinetic behavior of YDXNT using UPLC-QqQ-MS. The concentration of nine main constituents were in the range of 27.85-76.54 ng mL. This research provides a systematic approach for rapid qualitative analysis of absorbed constituents and for evaluating the pharmacokinetics of the main ingredients of YDXNT following its oral administration. More importantly, this work provides key information on the identification of bioactive compounds and the clarification of their action mechanisms, as well as on the pharmacological actions of YDXNT.
银丹心脑通软胶囊(YDXNT)是一种传统中药配方,已用于治疗心脑血管疾病数十年。先前的研究主要集中在评估YDXNT的药理特性和主要成分。然而,其多种生物活性成分仍知之甚少。在本研究中,采用超高效液相色谱-四极杆飞行时间质谱联用超高效液相色谱-三重四极杆质谱的综合策略,检测口服YDXNT后血浆中的吸收成分,并研究主要化合物的药代动力学。开发超高效液相色谱-四极杆飞行时间质谱用于检测大鼠口服给药后血浆中的吸收成分及其代谢产物。共鉴定或初步表征了52种成分,包括44种原型化合物和8种代谢产物。然后,选择9种主要化合物(槲皮素、异鼠李素、山奈酚、银杏内酯A、银杏内酯B、银杏内酯C、白果内酯、丹参酮IIA和丹酚酸B),使用超高效液相色谱-三重四极杆质谱进一步研究YDXNT的药代动力学行为。9种主要成分的浓度范围为27.85-76.54 ng/mL。本研究为快速定性分析吸收成分以及评估YDXNT口服后的主要成分药代动力学提供了一种系统方法。更重要的是,这项工作提供了有关生物活性化合物鉴定、作用机制阐明以及YDXNT药理作用的关键信息。