注射用散中亚胺培南含量的微生物测定方法

S. S. Oliveira, F. S. Barbosa, L. Pezzi, E. Schapoval, A. Mendez
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引用次数: 1

摘要

本工作描述了用柱板法定量测定注射用粉末中亚胺培南的微生物学方法的建立和验证。目的是获得一种低成本和合适的方法,可以替代已经描述的物理化学技术,有助于这种抗生素的质量控制。首先,对分析条件进行优化,对微生物、接种浓度、样品和标准浓度的最佳范围进行测试,以提供充分的抑制晕测量。以表皮葡萄球菌ATCC 12228为试验微生物,接种量为2.0%。验证方案遵循官方指南,评价参数为线性度、精密度(中间精密度和可重复性)和准确度。在0.5 ~ 2.0µg mL-1范围内的标准曲线r值均大于0.999,方差分析证实与线性无偏离(p值< 0.05)。该方法重复性RSD值为0.28 ~ 0.64,中间精密度RSD值为2.49。实验进行了3天,每天进行3次分析,共8个板。平均含量为101.05%。采用回收率试验评价准确度,标准回收率为101.70 ~ 107.90%,平均回收率为104.86%,满意。因此,所建立的微生物学方法是经过验证的,适合用于该药的定量测定,可用于质量控制常规。
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MICROBIOLOGICAL ASSAY FOR QUANTITATIVE DETERMINATION OF IMIPENEM IN POWDER FOR INJECTION
This work describes the development and validation of a microbiological method using the cylinder-plate assay for quantitative determination of imipenem in powder for injection. The aim was to obtain a low-cost and suitable methodology that can be alternative to physicochemical techniques already described, contributing for the quality control of this antibiotic. Firstly, the analytical conditions were optimized, testing the microorganism, inoculum concentration and best range of sample and standard concentrations, in a way that provides the adequate measurement of the inhibition halos. Staphylococcu s epidermidis ATCC 12228 was selected as test microorganism, as well as 2.0 % of inoculum concentration. The validation protocol followed the official guidelines, and the parameters evaluated were linearity, precision (intermediate precision and repeatability) and accuracy. All standard curves ranging 0.5-2.0 µg mL-1 showed r values higher than 0.999, and ANOVA confirmed that were no deviation from linearity (p-value < 0.05). The method also proved to be precise with RSD (relative standard deviation) values ranging 0.28-0.64 for repeatability and 2.49 for intermediate precision. It was performed three days of experiments, being three assays of eight plates a day. The drug mean content was 101.05%. Accuracy was assessed by recovery test, with standard recovery percentage of 101.70-107.90% (mean recovery = 104.86%), which was considered satisfactory. Therefore, the proposed microbiological method was considered validated and suitable for application in quantitative determination of this drug, being useful for quality control routine.
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