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一种用于在单波长下同时体外测定阿莫西林和甲硝唑的简单高效液相色谱法的开发与验证。

Development and validation of a simple HPLC method for simultaneous in vitro determination of amoxicillin and metronidazole at single wavelength.

作者信息

Tavakoli Naser, Varshosaz Jaleh, Dorkoosh Farid, Zargarzadeh Mohammad R

机构信息

Faculty of Pharmacy & Pharmaceutical Sciences Research Center, Isfahan University of Medical Sciences, Isfahan, Iran.

出版信息

J Pharm Biomed Anal. 2007 Jan 4;43(1):325-9. doi: 10.1016/j.jpba.2006.06.002. Epub 2006 Jul 21.

Abstract

A simple, rapid, sensitive and robust reversed phase-HPLC method was developed and validated to measure simultaneously the amount of amoxicillin and metronidazole at single wavelength (254 nm) in order to assess drug release profiles and drug-excipients compatibility studies for a new floating-sustained release tablet formulation and its subsequent stability studies. An isocratic elution of filtered sample was performed on C18 column with buffered mobile phase (pH 4.0) and UV detection at 254 nm. Quantification was achieved with reference to the external standards. The linearity for concentrations between 0.15 and 600 microg/ml for amoxicillin and 0.13 and 300 microg/ml for metronidazole were established. Intra and inter-day precision were less than 2.5%. The limits of detection (LOD) and quantification were 0.05 and 0.15 microg/ml for amoxicillin and 0.10 and 0.13 microg/ml for metronidazole. The determination of the two active ingredients was not interfered by the excipients of the products. Samples were stable in the release media (37 degrees C) and the HPLC injector at least for 12 h.

摘要

开发并验证了一种简单、快速、灵敏且稳健的反相高效液相色谱法,用于在单波长(254 nm)下同时测定阿莫西林和甲硝唑的含量,以评估一种新型胃漂浮缓释片剂制剂的药物释放曲线、药物-辅料相容性研究及其后续稳定性研究。将过滤后的样品在C18柱上进行等度洗脱,流动相为缓冲液(pH 4.0),并在254 nm处进行紫外检测。采用外标法进行定量。确定了阿莫西林浓度在0.15至600 μg/ml之间以及甲硝唑浓度在0.13至300 μg/ml之间的线性关系。日内和日间精密度均小于2.5%。阿莫西林的检测限(LOD)和定量限分别为0.05和0.15 μg/ml,甲硝唑的检测限和定量限分别为0.10和0.13 μg/ml。两种活性成分的测定不受产品辅料的干扰。样品在释放介质(37℃)和高效液相色谱进样器中至少稳定12小时。

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