原料和注射制剂中头孢匹罗的微生物测定方法

T. P. Oppe, Júlia Menegola, E. Schapoval
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引用次数: 5

摘要

头孢匹罗是抗广谱革兰氏阴性和革兰氏阳性细菌感染的第四代头孢菌素。本文描述了一种简单、灵敏、特异的琼脂扩散生物测定方法的建立和验证,该方法应用圆筒-平板法定量注射制剂原料和粉末中的头孢匹罗。验证方法具有良好的线性度、精密度、准确度和特异性。本实验以头孢匹罗为试验微生物,考察其对嗜枯病菌ATCC 9341的抑制作用。分析结果采用方差分析进行统计学处理,标准溶液和样品溶液的响应图在0.3 ~ 1.2µg mL-1范围内呈线性关系(r = 0.9948),精确(测定内:RSD = 0.11;测定间:RSD = 0.18),准确度高(平均回收率= 99.41%)。头孢匹罗的初步稳定性研究表明,微生物测定法对存在降解产物的头孢匹罗的测定具有特异性。该方法可用于头孢匹罗制剂剂型和原料的定量,可用于常规质量控制中的药物分析。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
MICROBIOLOGICAL ASSAY FOR THE DETERMINATION OF CEFPIROME IN RAW MATERIAL AND INJECTABLE PREPARATION
Cefpirome is a fourth-generation cephalosporin active against a broad spectrum of gram-negative and gram-positive bacterial infections. The present work describe the development and validation of a simple, sensitive and specific agar diffusion bioassay applying cylinder-plate method for quantification of cefpirome in raw material and powder for injectable preparation. The validation method yielded good results and included linearity, precision, accuracy and specificity. The assay is based on the inhibitory effect of cefpirome upon the strain of Kocuria rizophila ATCC 9341 as the test microorganism. The result of assay were treated statistically by ANOVA and the response graphs for standard and sample solutions were linear (r = 0.9948) in the range of 0.3 – 1.2 µg mL-1, precise (intra-assay: RSD = 0.11; inter-assay: RSD = 0.18) and accurate (mean recovery value = 99.41%). A preliminary stability study of cefpirome showed that the microbiological assay is specific for the determination cefpirome in the presence of its degradation products. The proposed microbiological method allows the quantitation of cefpirome in pharmaceutical dosage form and raw material and can be used for the drug analysis in routine quality control.
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