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作 者:南峰[1] 徐楠[1] 陈枳潓[1] 向瑾[1] 梁茂植[1] 陶泽婷 叶薇 NAN Feng;XU Nan;CHEN Zhihui;XIANG Jin;LIANG Maozhi;TAO Zeting;YE Wei(GCP Centre, West China Hospital of Sichuan University, Chengdu 610041, Sichuan, China)
机构地区:[1]四川大学华西医院GCP中心
出 处:《中国临床药理学与治疗学》2018年第1期73-77,共5页Chinese Journal of Clinical Pharmacology and Therapeutics
基 金:国家自然科学基金青年基金(30900493)
摘 要:目的:建立快速灵敏的LC-MS/MS法测定人血浆中阿莫西林浓度,并用于两种阿莫西林胶囊的一致性评价。方法:采用岛津公司LCMS-8060型LC-MS/MS仪,以MRM模式测定阿莫西林(m/z 366.00/114.00)的浓度,d4-阿莫西林作内标(m/z 370.10/114.05),离子源为ESI源。色谱柱选用Waters ACQUITY BEH C_(18)(2.1×50mm,1.7μm),梯度洗脱。血浆样本加入内标,经甲醇沉淀蛋白后取上清液进样检测。结果:所建方法经验证,其线性、准确度、精密度、最低定量限、提取回收率、特异性、基质效应、稳定性等各项指标均符合CFDA的指导原则及最新核查标准要求,并较文献报道中的方法有处理简单、灵敏度高、色谱峰形好的优点。结论:所建方法快速、灵敏,适用于人血浆中阿莫西林浓度的检测。用于一致性评价的样本实测,两种制剂生物等效。AIM: To establish a rapid and sensitive LC-MS/MS method for determination of amoxicillin in human plasma and to study the bioavailability of two amoxicillin capsules. METHODS:Shimadzu LCMS-8060 series LC-MS/MS was used.Amoxicillin( m/z 366. 00/114. 00) and d4-amoxicillin( internal standard,m/z 370. 10/114. 05) were monitored by ESI in MRM model. The analysts were eluted on Waters ACQUITY BEH C18 column( 2. 1× 50 mm,1. 7 μm) according to gradient elution program. The plasma samples were mixed with internal standard,then precipitated protein by methanol,the supernatants were detected. RESULTS: The linear,accuracy,precision,LLOQ,extraction recovery,specificity,matrix effect,stability of our method all met the guiding principles and criteria of CFDA. Compared with the literature reports,our method was simple,rapid,sensitive and had better chromatographic peaks. CONCLUSION: The method is rapid,sensitive and suitable for the determination of amoxicillin in human plasma. The test capsule is bioequivalence to the reference capsule.
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