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Development and Validation of a Successful Microbiological Agar Assay for Determination of Ceftriaxone Sodium in Powder for Injectable Solution

机译:成功的微生物琼脂测定法的建立和验证,该测定法可用于注射液粉末中的头孢曲松钠

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Ceftriaxone sodium is a cephalosporin with broad-spectrum antimicrobial activity and belongs to the third generation of cephalosporins. Regarding the quality control of medicines, a validated microbiological assay for the determination of ceftriaxone sodium in powder for injectable solution has not been reported yet. This paper reports the development and validation of a simple, accurate and reproducible agar diffusion method to quantify ceftriaxone sodium in powder for injectable solution. The assay is based on the inhibitory effect of ceftriaxone sodium on the strain of Bacillus subtilis ATCC 9371 IAL 1027 used as test microorganism. The results were treated statistically by analysis of variance and were found to be linear (r = 0.999) in the selected range of 15.0–60.0 μg/mL, precise with a relative standard deviation (RSD) of repeatability intraday = 1.40%, accurate (100.46%) and robust with a RSD lower than 1.28%. The results demonstrated the validity of the proposed bioassay, which allows reliable ceftriaxone sodium quantitation in pharmaceutical samples and therefore can be used as a useful alternative methodology for the routine quality control of this medicine.
机译:头孢曲松钠是具有广谱抗菌活性的头孢菌素,属于第三代头孢菌素。关于药物的质量控制,尚未有用于确定注射液粉末中头孢曲松钠含量的有效微生物测定方法的报道。本文报道了一种简单,准确和可重现的琼脂扩散方法的开发和验证,该方法可定量注射液粉末中的头孢曲松钠。该测定基于头孢曲松钠对用作测试微生物的枯草芽孢杆菌ATCC 9371 IAL 1027菌株的抑制作用。通过方差分析对结果进行统计学处理,发现结果在所选范围15.0–60.0μg/ mL内呈线性(r = 0.999),精确度为日内重复性的相对标准偏差(RSD)= 1.40%,准确度( 100.46%),且RSD低于1.28%。结果证明了所提出的生物测定方法的有效性,该方法可以对药物样品中的头孢曲松钠进行可靠的定量,因此可以用作该药物常规质量控制的有用替代方法。

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