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用于分析奥美拉唑、替硝唑、多西环素和克拉霉素的反相高效液相色谱/柱前衍生化法

RP-HPLC/pre-column derivatization for analysis of omeprazole, tinidazole, doxycycline and clarithromycin.

作者信息

Darwish Khaled M, Salama Ismail, Mostafa Samia, El-Sadek Mohamed

机构信息

Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Suez Canal University, Ismailia 41552, Egypt.

出版信息

J Chromatogr Sci. 2013 Jul;51(6):566-76. doi: 10.1093/chromsci/bms167. Epub 2012 Oct 18.

Abstract

A validated, reliable and accurate reversed-phase high performance liquid chromatographic method using pre-column derivatization was adopted for the simultaneous determination of two ternary mixtures containing omeprazole, tinidazole and doxycycline hyclate or clarithromycin. Separation was achieved on a C18 column, through a gradient elution system using acetonitrile-methanol-water adjusted to pH = 6.60. Drugs were detected at 277 nm over concentration ranges of 1-112, 5-125, 2.5-550 and 2.5-100 µg/mL for omeprazole, tinidazole, doxycycline hyclate and clarithromycin, respectively. This is the first method that has isolated and identified clarithromycin derivative by infrared and mass spectroscopy. This method is the first study for the simultaneous determination of omeprazole, tinidazole, doxycycline hyclate and clarithromycin in combined mixtures and pharmaceutical formulations.

摘要

采用经过验证的、可靠且准确的柱前衍生反相高效液相色谱法,同时测定含奥美拉唑、替硝唑和盐酸多西环素或克拉霉素的两种三元混合物。在C18柱上进行分离,通过使用pH值调至6.60的乙腈 - 甲醇 - 水的梯度洗脱系统实现。奥美拉唑、替硝唑、盐酸多西环素和克拉霉素的检测波长均为277 nm,浓度范围分别为1 - 112、5 - 125、2.5 - 550和2.5 - 100 μg/mL。这是首次通过红外光谱和质谱分离并鉴定克拉霉素衍生物的方法。该方法是首次对联合混合物和药物制剂中奥美拉唑、替硝唑、盐酸多西环素和克拉霉素进行同时测定的研究。

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