Zhang Zhixin, Qin Lingling, Peng Long, Zhang Qingqing, Wang Qing, Lu Zhiwei, Song Yuelin, Gao Xiaoyan
School of Chinese Pharmacy, Beijing University of Chinese Medicine, South of Wangjing Middle Ring Road, Chaoyang District, Beijing 100102, China.
Modern Research Center for Traditional Chinese Medicine, Beijing University of Chinese Medicine, No. 11 North Third Ring Road, Chaoyang District, Beijing 100029, China.
Molecules. 2016 Mar 7;21(3):317. doi: 10.3390/molecules21030317.
Qingkailing injection (QKLI) is a modern Chinese medicine preparation derived from a well-known classical formulation, An-Gong-Niu-Huang Wan. Although the clinical efficacy of QKLI has been well defined, its severe adverse drug reactions (ADRs) were extensively increased. Through thorough attempts to reduce ADR rates, it was realized that the effect-based rational use plays the key role in clinical practices. Hence, the pharmacokinetic-pharmacodynamic (PK-PD) model was introduced in the present study, aiming to link the pharmacokinetic profiles with the therapeutic outcomes of QKLI, and subsequently to provide valuable guidelines for the rational use of QKLI in clinical settings. The PK properties of the six dominant ingredients in QKLI were compared between the normal treated group (NTG) and the pyrexia model group (MTG). Rectal temperatures were measured in parallel with blood sampling for NTG, MTG, model control group (MCG), and normal control group (NCG). Baicalin and geniposide exhibited appropriate PK parameters, and were selected as the PK markers to map the antipyretic effect of QKLI. Then, a PK-PD model was constructed upon the bacalin and geniposide plasma concentrations vs. the rectal temperature variation values, by a two-compartment PK model with a Sigmoid Emax PD model to explain the time delay between the drug plasma concentration of PK markers and the antipyretic effect after a single dose administration of QKLI. The findings obtained would provide fundamental information to propose a more reasonable dosage regimen and improve the level of individualized drug therapy in clinical settings.
清开灵注射液(QKLI)是一种源自著名经典方剂安宫牛黄丸的现代中药制剂。尽管QKLI的临床疗效已得到明确,但它的严重药物不良反应(ADR)却大幅增加。通过全面努力降低ADR发生率,人们认识到基于效应的合理用药在临床实践中起着关键作用。因此,本研究引入了药代动力学 - 药效学(PK - PD)模型,旨在将药代动力学特征与QKLI的治疗效果联系起来,进而为QKLI在临床环境中的合理使用提供有价值的指导。比较了正常治疗组(NTG)和发热模型组(MTG)中QKLI六种主要成分的药代动力学特性。对NTG、MTG、模型对照组(MCG)和正常对照组(NCG)同时进行直肠温度测量和采血。黄芩苷和栀子苷表现出合适的药代动力学参数,并被选为药代动力学标志物来描绘QKLI的解热作用。然后,基于黄芩苷和栀子苷的血浆浓度与直肠温度变化值,通过具有Sigmoid Emax药效学模型的二室药代动力学模型构建了PK - PD模型,以解释单次给药QKLI后药代动力学标志物的药物血浆浓度与解热作用之间的时间延迟。所获得的研究结果将为提出更合理的给药方案和提高临床环境中个体化药物治疗水平提供基础信息。