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采用超高效液相色谱-串联质谱法研究比格犬中[具体草药名称]与格列吡嗪的药代动力学相互作用

Pharmacokinetics Study of Herb-Drug Interaction of and Glipizide in Beagle Dogs Using UPLC-MS/MS.

作者信息

Qi He, Wang Wenjiong, Zhang Xianghan, Shang Bingyang

机构信息

Innovation Practice Platform for College Student, College of Basic Medicine and Forensic Medicine, Henan University of Science and Technology, Luoyang, Henan, China.

出版信息

Int J Anal Chem. 2025 Jul 28;2025:7941435. doi: 10.1155/ianc/7941435. eCollection 2025.

DOI:10.1155/ianc/7941435
PMID:40761345
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12321411/
Abstract

Based on the establishment and validation of a UPLC-MS/MS method for detecting glipizide in beagle plasma, the herb-drug interaction (HDI) between berberine and glipizide was studied. After gradient elution separation of glipizide and internal standard, multiple reaction monitoring was used for detection in positive ion mode. The ion reactions used for quantitative analysis were glipizide m/z 446.0 ⟶ 321.0 and IS m/z 307.1 ⟶ 220.0. Six beagle dogs were treated with glipizide alone and berberine intervention, and the pharmacokinetic changes of glipizide were compared. The UPLC-MS/MS method has good linearity and the advantages of being green, simple, sensitive, and fast. After continuous administration of berberine to beagle dogs for 7 days, the pharmacokinetic process of glipizide changed with , AUC and AUC increasing, t prolonging, and CL and Vd decreasing. When using combination therapy, attention should be paid to possible HDI.

摘要

基于建立和验证用于检测比格犬血浆中格列吡嗪的超高效液相色谱-串联质谱(UPLC-MS/MS)方法,研究了黄连素与格列吡嗪之间的药-药相互作用(HDI)。对格列吡嗪和内标进行梯度洗脱分离后,采用多反应监测在正离子模式下进行检测。用于定量分析的离子反应为格列吡嗪m/z 446.0→321.0和内标m/z 307.1→220.0。对6只比格犬分别进行单独给予格列吡嗪和黄连素干预处理,并比较格列吡嗪的药代动力学变化。该UPLC-MS/MS方法具有良好的线性,且具有绿色、简便、灵敏和快速的优点。对比格犬连续7天给予黄连素后,格列吡嗪的药代动力学过程发生改变, 、AUC和AUC增加,t延长,CL和Vd降低。联合治疗时应注意可能存在的药-药相互作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb3d/12321411/7c497a973ea2/IJAC2025-7941435.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb3d/12321411/1492fef3d021/IJAC2025-7941435.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb3d/12321411/7c497a973ea2/IJAC2025-7941435.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb3d/12321411/1492fef3d021/IJAC2025-7941435.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb3d/12321411/7c497a973ea2/IJAC2025-7941435.002.jpg

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本文引用的文献

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Inhibition of N6-methyladenosine methylation of ASC by berberine ameliorates pyroptosis of renal tubular epithelial cells in acute kidney injury.黄连素抑制ASC的N6-甲基腺苷甲基化可改善急性肾损伤中肾小管上皮细胞的焦亡。
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Berberine Ameliorates High-fat-induced Insulin Resistance in HepG2 Cells by Modulating PPARs Signaling Pathway.
小檗碱通过调节过氧化物酶体增殖物激活受体(PPARs)信号通路改善高脂诱导的HepG2细胞胰岛素抵抗。
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