白芍、雷公藤总苷与塞来昔布在Beagle犬体内的相互作用

IF 1.9 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Zhifei Zhang, Huijun Wang, Xinli Ren, Xiaotong Li, Xinyu Peng, Xiangjun Qiu
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引用次数: 0

摘要

背景与目的:芍药总苷(TGP)胶囊、雷公藤糖苷片(TGT)和塞来昔布是临床治疗类风湿性关节炎(RA)的常用药物。建立了塞来昔布在beagle犬体内的超高效液相色谱-质谱联用分析方法,基于药代动力学研究了TGP和TGT与塞来昔布的药物相互作用。方法:采用乙腈沉淀法处理血浆样品。采用梯度洗脱法分离塞来昔布和呋塞米(内标,IS),在正离子下采用多反应监测模式进行检测。用于定量分析的离子反应:塞来昔布为m/z 379.82→315.82,IS为m/z 328.74→204.88。hdi实验采用三阶段实验设计。在第一阶段,6只比格犬口服6.67 mg/kg塞来昔布。第二期给药TGP 20 mg/kg,每天2次,连续7 d,然后口服塞来昔布。第三期口服TGT 1.5 mg/kg,每天2次,连续7 d,然后口服塞来昔布。检测塞来昔布在三个时期的浓度,并根据药代动力学评价hdi。结果:塞来昔布在10 ~ 2000 ng/mL范围内线性良好。准确度、精密度、回收率、基质效应、稳定性均达到标准要求。当塞来昔布与TGPC或TGT合用时,塞来昔布的主要药动学参数发生变化,Cmax、AUC(0-t)和AUC(0-∞)升高,t½延长,CL和Vd降低。结论:建立了一种新的超高效液相色谱-质谱联用方法,可用于比格犬血浆中塞来昔布的测定。TGP和TGT可抑制比格犬对塞来昔布的代谢,从而影响塞来昔布的药动学参数,增加塞来昔布的血浆暴露量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Herb-Drug Interaction of Total Glucosides of Paeony and Tripterygium Glycoside with Celecoxib in Beagle Dogs by UPLC-MS/MS.

Background and objective: Total glucosides of paeony (TGP) capsules, tripterygium glycoside tablets (TGT), and celecoxib are commonly used drugs in clinical practice for the treatment of Rheumatoid arthritis (RA). An UPLC-MS/MS method for the analysis of celecoxib in beagle dogs was developed, the herb-drug interactions (HDIs) between TGP and TGT with celecoxib were studied based on pharmacokinetics.

Methods: The method of acetonitrile precipitation was applied to process plasma samples. Celecoxib and furosemide (internal standard, IS) was separated by gradient elution, and detected using multiple reaction monitoring mode under the positive ion. The ion reactions used for quantitative analysis were m/z 379.82 → 315.82 for celecoxib, and m/z 328.74 → 204.88 for IS. HDIs experiments adopt a three-stage experimental design. In the first period, six beagle dogs was orally administered 6.67 mg/kg celecoxib. In the second period, TGP 20 mg/kg was given orally twice a day for 7 consecutive days, then celecoxib was orally administered. And, in the third period, TGT 1.5 mg/kg was orally given, twice a day for 7 consecutive days, then celecoxib was orally administered. The concentration of celecoxib in the three periods was detected, and HDIs were evaluated based on pharmacokinetics.

Results: Celecoxib exhibited good linearity in the range of 10-2000 ng/mL. The accuracy, precision, recoveries, matrix effects, and stability all met the standards. When celecoxib was used in combination with TGPC or TGT, the main pharmacokinetic parameters of celecoxib changed, Cmax, AUC(0-t) and AUC(0-∞) increased, t½ was prolonged, and CL and Vd decreased.

Conclusion: A novel UPLC-MS/MS approach was successfully performed and applied to measure celecoxib in beagle dog plasma. TGP and TGT could inhibit the metabolism of celecoxib in beagle dogs, thereby affecting the pharmacokinetic parameters of celecoxib and increasing plasma exposure to celecoxib.

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来源期刊
CiteScore
3.70
自引率
0.00%
发文量
64
审稿时长
>12 weeks
期刊介绍: Hepatology International is a peer-reviewed journal featuring articles written by clinicians, clinical researchers and basic scientists is dedicated to research and patient care issues in hepatology. This journal focuses mainly on new and emerging diagnostic and treatment options, protocols and molecular and cellular basis of disease pathogenesis, new technologies, in liver and biliary sciences. Hepatology International publishes original research articles related to clinical care and basic research; review articles; consensus guidelines for diagnosis and treatment; invited editorials, and controversies in contemporary issues. The journal does not publish case reports.
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