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气相色谱法和火焰离子化检测器(GC-FID)同时测定不同剂型中的硝酸咪康唑和甲硝唑

Simultaneous Determination of Miconazole Nitrate and Metronidazole in Different Pharmaceutical Dosage Forms by Gas Chromatography and Flame Ionization Detector (GC-FID).

作者信息

Ashour Safwan, Kattan Nuha

机构信息

Bioanalytical Laboratory, Department of Chemistry, Faculty of Science, University of Aleppo, Aleppo, Syria.

出版信息

Int J Biomed Sci. 2010 Mar;6(1):13-8.

Abstract

A simple, rapid and precise gas chromatographic method has been developed for the simultaneous determination of miconazole nitrate (MIZ) and metronidazole (MNZ) in tablets and ovules, using a capillary column AE.SE-54 (15 m × 0.53 mm, i.d.) and nitrogen as a carrier gas at a flow rate of 9 mL min(-1). The oven temperature was programmed at 140°C for 3 min, with a rise of 40°C min(-1) up to 180°C (held for 2 min) and then increased to a final temperature of 250°C. The injector and detector port temperatures were maintained at 260°C. Detection was carried out using flame ionization detector. Results of assay and recovery studies were statistically evaluated for its accuracy and precision. The retention times were about 3.50 and 12.90 min for MNZ and MIZ, respectively. Linearity ranges were 50.0-6030.0 and 62.5-2000.0 μg mL(-1) for MNZ and MIZ, with limit of detection values of 2.5 and 3.1 μg mL(-1), respectively. Correlation coefficients (R(2)) of the regression equations were greater than 0.999 in all cases. No interference from any components of pharmaceutical dosage forms or degradation products was observed. According to the validation results, the proposed method was found to be specific, accurate, precise and could be applied to the simultaneous quantitative analysis of MIZ and MNZ in tablets and ovules.

摘要

已开发出一种简单、快速且精确的气相色谱法,用于同时测定片剂和栓剂中的硝酸咪康唑(MIZ)和甲硝唑(MNZ)。使用毛细管柱AE.SE - 54(15 m×0.53 mm,内径),以氮气作为载气,流速为9 mL min(-1)。柱温程序设定为在140°C保持3 min,然后以40°C min(-1)的速率升至180°C(保持2 min),再升至最终温度250°C。进样口和检测器端口温度保持在260°C。采用火焰离子化检测器进行检测。对含量测定和回收率研究的结果进行统计学评估,以确定其准确性和精密度。MNZ和MIZ的保留时间分别约为3.50和12.90 min。MNZ和MIZ的线性范围分别为50.0 - 6030.0和62.5 - 2000.0 μg mL(-1),检测限分别为2.5和3.1 μg mL(-1)。所有情况下回归方程的相关系数(R(2))均大于0.999。未观察到药物剂型的任何成分或降解产物产生干扰。根据验证结果,该方法具有特异性、准确性、精密度,可用于片剂和栓剂中MIZ和MNZ的同时定量分析。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c1e/3614734/f6e1936ebafe/IJBS-06-013-g001.jpg

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