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一种用于分析活血止痛橡胶膏中3种生物活性成分的MD-LC-MS/MS方法的建立及其在大鼠体内的药代动力学研究中的应用

Development of a MD-LC-MS/MS Method to Analyze 3 Bioactive Compounds in Huoxuezhitong Rubber Patch and Application to a Pharmacokinetic Study in Rats.

作者信息

Cui Yahua, Yang Chang, Liang Jun, Zhong Linying, Liu Caifeng, Bai Jie, Du Shouying, Liu Daofang

机构信息

School of Chinese Materia Medica, Beijing University of Chinese Medicine, Fangshan District 102488, Beijing, China.

An Hui An Ke Yu Liang Qing Pharmaceutical Co., Ltd, Anqing 246001, Anhui, China.

出版信息

Evid Based Complement Alternat Med. 2019 Jan 17;2019:6173565. doi: 10.1155/2019/6173565. eCollection 2019.

Abstract

Huoxuezhitong rubber patch, a well-known traditional Chinese medicine (TCM) prescription, is utilized to treat pain and inflammation. In this study, a microdialysis-ultra-high-performance liquid chromatography-tandem mass spectrometry (MD-LC-MS/MS) method was designed for the simultaneous determination of active constituents in the rubber patch, such as paeonol (Pae), eugenol (Eug), and piperine (Pip). A microdialysis probe was implanted in the subcutaneous tissue of a rat, which is intended to detect the subcutaneous concentrations of target components. Saline containing 30% ethanol acted as perfusion fluid. Analytes in the microdialysate were completely separated over an ACQITY UPLC RBEH C column (2.1mm×100mm, 1.7m). The mobile phase was composed of 0.01% ammonia aqueous and acetonitrile-0.01% ammonia with gradient elution. The single-run analysis time was 10.0 minutes. The linear regression displayed good linear relationships in the ranges of 0.25-100 ng/mL for paeonol and eugenol and 0.001-5 ng/mL for piperine. The interday and intraday precision of the quality control samples exhibited relative standard deviations (RSD) <13.56%. The accuracy values ranged from -14.92% to 14.00%. The present method was successfully applied in pharmacokinetics studies following dermal administration of Huoxuezhitong rubber patch in rats. Pip's T (488.00±150.73) min was greater than that of Pae (186.67±48.44) min and Eug (240.00±138.56) min, and the rank order of t was Pae > Pip > Eug. The rank order of AUC and C was both Eug > Pae > Pip. MRT of Pip was higher than that of Pae and Eug. Eugenol showed a faster elimination and a shorter half-life. Paeonol showed a stronger drug reservoir function after removing the drug source.

摘要

活血止痛贴是一种著名的中药方剂,用于治疗疼痛和炎症。在本研究中,设计了一种微透析-超高效液相色谱-串联质谱(MD-LC-MS/MS)方法,用于同时测定贴剂中的活性成分,如丹皮酚(Pae)、丁香酚(Eug)和胡椒碱(Pip)。将微透析探针植入大鼠皮下组织,旨在检测目标成分的皮下浓度。含30%乙醇的生理盐水作为灌注液。微透析液中的分析物在ACQITY UPLC RBEH C柱(2.1mm×100mm,1.7μm)上完全分离。流动相由0.01%氨水和乙腈-0.01%氨水组成,采用梯度洗脱。单次分析时间为10.0分钟。线性回归显示,丹皮酚和丁香酚在0.25-100 ng/mL范围内、胡椒碱在0.001-5 ng/mL范围内呈现良好的线性关系。质控样品的日间和日内精密度表现为相对标准偏差(RSD)<13.56%。准确度值范围为-14.92%至14.00%。本方法成功应用于大鼠经皮给予活血止痛贴后的药代动力学研究。胡椒碱的T(488.00±150.73)分钟大于丹皮酚(186.67±48.44)分钟和丁香酚(240.00±138.56)分钟,t的排序为丹皮酚>胡椒碱>丁香酚。AUC和C的排序均为丁香酚>丹皮酚>胡椒碱。胡椒碱的平均滞留时间高于丹皮酚和丁香酚。丁香酚显示出更快的消除和更短的半衰期。去除药物来源后,丹皮酚显示出更强的药物储库功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcda/6354162/9bdba505913c/ECAM2019-6173565.001.jpg

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