梁新丽 廖正根 王光发 赵国巍 戴春兰 张晓辉. 白芷提取物与延胡索总碱配伍对延胡索乙素在大鼠体内药代动力学的影响J. 药学学报, 2009,44(6): 645-650.
引用本文: 梁新丽 廖正根 王光发 赵国巍 戴春兰 张晓辉. 白芷提取物与延胡索总碱配伍对延胡索乙素在大鼠体内药代动力学的影响J. 药学学报, 2009,44(6): 645-650.
LIANG Xin-Li, LIAO Zheng-Gen, WANG Guang-Fa, DIAO Guo-Wei, DAI Chun-Lan, ZHANG Xiao-Hui. Influence of combination of extractum Angelicae Dahuricae Siccum and total alkaloids of Rhizoma Corydalis on pharmacokinetics of tetrahydropalmatine in ratsJ. 药学学报, 2009,44(6): 645-650.
Citation: LIANG Xin-Li, LIAO Zheng-Gen, WANG Guang-Fa, DIAO Guo-Wei, DAI Chun-Lan, ZHANG Xiao-Hui. Influence of combination of extractum Angelicae Dahuricae Siccum and total alkaloids of Rhizoma Corydalis on pharmacokinetics of tetrahydropalmatine in ratsJ. 药学学报, 2009,44(6): 645-650.

白芷提取物与延胡索总碱配伍对延胡索乙素在大鼠体内药代动力学的影响

Influence of combination of extractum Angelicae Dahuricae Siccum and total alkaloids of Rhizoma Corydalis on pharmacokinetics of tetrahydropalmatine in rats

  • 摘要:

    建立一种快速灵敏的大鼠体内延胡索乙素 (tetrahydropalmatineTET) 血药浓度的HPLC-FLD检测方法;并研究白芷香豆素 (coumarinCou) 和挥发油 (volatile oilVO) 两种提取物与延胡索总碱 (TA) 配伍对TET在大鼠体内药代动力学的影响。血浆经正己烷-异丙醇 (955) 沉淀蛋白,HPLC-FLD检测,结果血浆中TET的线性范围为2.096167.68 μg·L−1;定量限2.096 μg·L−1;方法准确度94.0%100.0%,提取回收率72.0%81.5%,日内日间精密度均小于7.0%;大鼠灌胃TATA-VOTA-CouTA-VO-Cou后,TET在大鼠体内药代动力学行为均为二室开放模型,与TA组相比,配伍VO() CouTETAUC0−tAUC0−∞MRT0−tMRT0−∞等药代动力学参数有显著差异。建立的大鼠血浆中TET的测定方法具有灵敏、准确、专属性强等特点;CouVOTA配伍,能显著延长TET在大鼠体内滞留时间,减缓体内的消除,提高其生物利用度。

     

    Abstract:

    This paper is aimed to develop a rapid and sensitive HPLC-fluorescence detection (FLD) method for the determination of tetrahydropalmatine (TET) in rats’ plasma.  The influence of combinations of Extractum Angelicae Dahuricae Siccum (coumarin and volatile oil) and total alkaloids (TA) from Rhizoma Corydalis (TA) on pharmacokinetics of TET in rats was studied.  Plasma samples were treated with hexane-isopropanol (955) to precipitate the protein, and were determined by HPLC-fluorescence detection.  The calibration curve was linear in the range of 2.096−167.68 μg·L−1.  The limit of quantification was 2.096 μg·L−1.  The method recovery of TET was 94.0%−100.0%.  The extract recovery was 72.0%−81.5%.  RSDs of intra- and inter-day precisions were all less than 7.0%.  Pharmacokinetics of TET in rats was fitted to two compartments open model after oral administration of TA, TA-volatile oil (VO), TA-coumarin (Cou) and TA-VO-Cou.  Compared with TA, AUC0−t, AUC0−∞, MRT0−t and MRT0−∞ of TET had significant deviation when combined with VO and/or Cou.  The   determination method is sensitive, specific, accurate, and appropriate for determination of TET in vivo.  Coumarin and/or VO combined with TA can prolong the resistance time of TET significantly, delay elimination and     enhance bioavailability of tetrahydropalmatine.

     

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