Pharmacokinetics of Gentiopicroside in Total Iridoid Glucosides Extracted from in Rats
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Pharmacokinetics of Gentiopicroside in Total Iridoid Glucosides Extracted from in Rats
Chinese Journal of Experimental Traditional Medical FormulaeVol. 18, Issue 22, Pages: 176-179(2012)
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Published:2012
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CUI Chun-li, TANG Zhi-shu, GUO Dong-yan, et al. Pharmacokinetics of Gentiopicroside in Total Iridoid Glucosides Extracted from in Rats[J]. Chinese journal of experimental traditional medical formulae, 2012, 18(22): 176-179.
DOI:
CUI Chun-li, TANG Zhi-shu, GUO Dong-yan, et al. Pharmacokinetics of Gentiopicroside in Total Iridoid Glucosides Extracted from in Rats[J]. Chinese journal of experimental traditional medical formulae, 2012, 18(22): 176-179.DOI:
Pharmacokinetics of Gentiopicroside in Total Iridoid Glucosides Extracted from in Rats
Objective:To establish a rapid RP-HPLC method for the determination and to study the pharmacokinetics of gentiopicroside after ig the total iridoid glucosides (TIG) extracted from Gentiana macophlla in rats and to assess the effect of other component in the TIG extracted from Gentiana macophlla. Method: The rats were orally treated with the TIG extracted from Gentiana macophlla. Plasma in centrifuge tube heparinized was separated by centifugation at 4 000 r·min-1 for 10 min
and five times acetonitrile in volume was added to deposit proteins. After centrifugalized
the concentration of gentiopicroside in plasma was determined by RP-HPLC. The pharmacokinetic parameters were calculated with Kinetic software. Result: A good linear relationship was obtained between the peak area and the concentration of gentiopicroside from 33.5 to 4 020.0 μg·L-1
and the lowest limit of detection of gentiopicroside in plasma was 6.7 μg·L-1. The mean extraction recoveries were 80.82%
97.38% and 89.10% for high
middle
low concentrations of the samples respectively. The concentration-time profiles of gentiopicroside were fit with noncompartment model. The main pharmacokinetics parameters t1/2
Tmax
Cmax
MRT
HVD
AUC(0~∞)
CL(s) were relatively stable. Conclusion: The method applied for determination of gentiopicroside content in blood was quick
simple
accurate
sensitive and feasible for the study of the gentiopicroside pharmacokinetics in rats.
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Related Author
GE Wei-hong1
GUO Jian-you2
CAI Jin-na3
XUE Jian-guo3
LIU Yue-qing3
DENG Ya-li
ZHOU Li-ling
FENG Su-xiang
Related Institution
Institute of Medicinal Plant,Yunnan Academy of Agricultural Sciences
College of Life Science,Yunnan University
Institute of Chinese Materia Medica,China Academy of TCM
中国中医研究院中药研究所 北京100700
Affiliated Hospital of Nanjing University of Chinese Medicine