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UHPLC-UV和HPLC-UV法同时测定一线四联抗结核药物的比较研究

Simultaneous Determination of First-Line 4-FDC Antituberculosis Drugs by UHPLC-UV and HPLC-UV: A Comparative Study.

作者信息

Franco Pedro H C, Chellini Paula R, Oliveira Marcone A L, Pianetti Gerson A

机构信息

Universidade Federal de Minas Gerais, Faculdade de Farmácia, Departamento de Produtos Farmacêuticos, Avenida Presidente Antônio Carlos 6627, 31270-901 Belo Horizonte, MG, Brazil.

Universidade Federal de Juiz de Fora, Faculdade de Farmácia, Departamento de Ciências Farmacêuticas, Rua José Lourenço Kelmer, 36036-900 Juiz de Fora, MG, Brazil.

出版信息

J AOAC Int. 2017 Jul 1;100(4):1008-1015. doi: 10.5740/jaoacint.16-0200.

Abstract

Tuberculosis is the second most deadly infectious disease, surpassed only by HIV/AIDS, and has resulted in over 1 billion deaths in the last 200 years. The World Health Organization estimates that in 2014, 9.6 million people were infected by this disease and 1.5 million had died. First-choice treatment consists of fixed-dose combination tablets containing rifampicin, isoniazid, pyrazinamide, and ethambutol hydrochloride (4-FDC). There are pharmacopeial protocols available to test 4-FDC, but they are prolonged, two-step methods. One single-step method in the literature performs the simultaneous determination by HPLC, but requires a long acquisition time. In this context, an ultra-HPLC (UHPLC) method was developed based on the HPLC method with the objective of reducing analysis time. A C18 column (1.9 µm particle size) was used with UV-diode-array detection at 238 and 282 nm. The method was found to be selective, linear, exact, precise, and robust. Samples from two batches were analyzed and the results compared with those obtained by the HPLC method, with no statistically significant differences observed (P > 0.05). This UHPLC method reduced the analysis time from 17 to 4 min, with a more than 90% reduction in sample and reagent consumption and a financial economy of almost 50-fold.

摘要

结核病是第二大致命传染病,仅次于艾滋病毒/艾滋病,在过去200年中已导致超过10亿人死亡。世界卫生组织估计,2014年有960万人感染此病,150万人死亡。一线治疗方案包括含有利福平、异烟肼、吡嗪酰胺和盐酸乙胺丁醇的固定剂量复方片剂(4-FDC)。有药典规程可用于检测4-FDC,但它们是耗时较长的两步法。文献中的一种单步法通过高效液相色谱法(HPLC)进行同时测定,但需要较长的采集时间。在此背景下,基于HPLC法开发了一种超高效液相色谱法(UHPLC),目的是缩短分析时间。使用了粒径为1.9 µm的C18柱,并在238和282 nm处采用紫外二极管阵列检测。该方法具有选择性、线性、准确性、精密度和稳健性。对两批样品进行了分析,并将结果与HPLC法获得的结果进行比较,未观察到统计学上的显著差异(P>0.05)。这种UHPLC法将分析时间从17分钟缩短至4分钟,样品和试剂消耗量减少了90%以上,成本节约了近50倍。

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