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纸质出版日期:2014
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刘学伟, 刘爽, 黄树明. 抗老年性痴呆复方开心散有效提取物血清药物化学研究[J]. 中国实验方剂学杂志, 2014,20(6):179-183.
LIU Xue-wei, LIU Shuang, HUANG Shu-ming. Plasma Pharmacochemistry Study of Effective Extracivet from Kai-xinsan on Alzhemer’s Disease[J]. Chinese journal of experimental traditional medical formulae, 2014, 20(6): 179-183.
刘学伟, 刘爽, 黄树明. 抗老年性痴呆复方开心散有效提取物血清药物化学研究[J]. 中国实验方剂学杂志, 2014,20(6):179-183. DOI: 10.11653/syfj2014060179.
LIU Xue-wei, LIU Shuang, HUANG Shu-ming. Plasma Pharmacochemistry Study of Effective Extracivet from Kai-xinsan on Alzhemer’s Disease[J]. Chinese journal of experimental traditional medical formulae, 2014, 20(6): 179-183. DOI: 10.11653/syfj2014060179.
目的:分析开心散60%乙醇提取物(KXS-60%E)体外各成分的归属来源及大鼠灌服KXS-60%E后药物入血成分。方法:应用UPLC-TOF-MS技术建立KXS-60%E体外成分以及大鼠灌服药物后含药血清样品的分析方法,根据各单味药的色谱峰确定全方主要成分的来源归属;对比空白血清、含药血清的成分异同,分析药物的入血成分。结果:通过对比KXS-60%E与各单味药的正负总离子流图,归属了94个主要色谱峰的来源;大鼠口服KXS-60%E后,在血中分析指定了41个入血成分,其中13个为新产生的代谢产物,28个成分为KXS-60%E的原形成分。结论:血中移行成分及其代谢产物是KXS-60%E防治老年性痴呆(AD)的更直接药效物质基础,对其进行深入的研究将有助于阐明开心散防治AD的作用机制。
Objective: To analyse the origin of peaks in Kaixinsan(KXS) extracted by 60% ethano(KXS-60% E)l and the constituents in rat plasma after oral administration of KXS-60% E. Method: A UPLC-TOF-MS method for analyzing the constituents in KXS-60% E and in rat plasma after oral administration of KXS-60% E
has been established.The origin of peaks in KXS-60% E were pointed out compared with each single herb in the formula similarly
the origin of peaks in treated serum after oral KXS-60% E were identified by contrasting the control rat serum. Result: Ninty-four compounds were detected in KXS-60% E in vitro
by compare with control rat plasma
41 peaks were pointed out in treated plasma.Concluding 28 original form in KXS-60% E and 13 metabolites. Conclusion: The constituents absorbed into blood and their metabolites of KXS-60% E were the direct basis of action of the drug
further study on these constituents may clarify the mechanism of KXS prevention and treatment on Alzhemer's disease.
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