汪晴

个人信息Personal Information

教授

博士生导师

硕士生导师

性别:男

毕业院校:日本国立九州工业大学

学位:博士

所在单位:化工学院

学科:药剂学. 药物工程

办公地点:大连理工大学制药科学与技术学院 G202

联系方式:0411-84986176

电子邮箱:qwang@dlut.edu.cn

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Pharmacokinetics and pharmacodynamics of glycyrrhetinic acid with Paeoniflorin after transdermal administration in dysmenorrhea model mice

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论文类型:期刊论文

发表时间:2016-07-15

发表刊物:PHYTOMEDICINE

收录刊物:SCIE、PubMed、Scopus

卷号:23

期号:8

页面范围:864-871

ISSN号:0944-7113

关键字:Glycyrrhetinic acid; Paeoniflorin; Pharmacokinetics; Pharmacodynamics; Analgesic; Transdermal drug delivery

摘要:Background: Glycyrrhetinic acid (GA) and paeoniflorin (PF) are the main active ingredients in Chinese peony-Liquorice Decoction, a widely used Traditional Chinese Medicine.
   Hypothesis/Purpose: The aim of this work was to investigate the combinatory analgesic effect of GA and PF after percutaneous administration and to define their pharmacokinetic/pharmacodynamic (PK/PD) characteristics.
   Study design and Methods: GA and PF were produced to transdermal patches based on previous research, and the permeation parameters of GA and PF in the patches were investigated with in vitro experiments. Dysmenorrhea model mice were then produced to compare the analgesic effects of the patches with different proportions of GA-PF. In the in vivo assessment, the number of writhes exhibited by the dysmenorrhea mice was recorded at designated time points, and skin, muscle under skin and plasma samples were collected, for assessments of drug distribution, pharmacokinetics parameters and PK/PD characteristics.
   Results and conclusion: In dysmenorrhea mice, GA-PF and meloxicam (the positive control drug) could relieve pain to equal degrees. Specifically, a single dose of the optimized patches (10% GA-10% PF, wt) exerted a steady analgesic effect for 48 h in dysmenorrhea mice, but this effect lagged behind the changes in the plasma concentration. Evaluation with the Bliss Independence criterion revealed that the two ingredients displayed a synergistic effect. Then the PK/PD relationship of GA in this compound preparation was defined with this synergistic effect. The preparation might be suitable for topical spasmolysis and anti-inflammatory therapy. (C) 2016 Elsevier GmbH. All rights reserved.