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A Rapid Validated RP-HPLC Method for the Simultaneous Determination of Cleaning Validation and Cross-Contamination of 12 Beta-Lactam Compounds

机译:快速有效的RP-HPLC方法用于同时测定12种β-内酰胺化合物的清洁验证和交叉污染

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摘要

The present work reports a rapid reversed-phase high-performance liquid chromatography (RP-HPLC) method for the simultaneous determination of 12 beta-lactam components for cleaning validation and cross-contamination. A strategic experimental approach was implemented for the method development. The desired chromatographic separation was achieved on a Symmetry C18 (4.6 X 75 mm, 3.5 μm) column using gradient elution. The optimized mobile phase consisted of the buffer tetrabutylammonium hydroxide pH-6.8 and acetonitrile. The eluted compounds were monitored at 215 nm and 254 nm wavelength using a photodiode array detector. The developed method separated 12-beta-lactam compounds from each other within a run time of 50 min. The method is effective for the determination of cross-contamination of penicillin and cephalosporin production blocks. The present method is specific and a lower limit of quantification was determined on the basis of the signal-to-noise ratio method; it is 1 μg/mL for all components. The developed RP-HPLC method was validated according to the International Conference on Harmonization (ICH) guidelines.
机译:本工作报告了一种快速反相高效液相色谱(RP-HPLC)方法,用于同时测定12种β-内酰胺成分,以进行清洁验证和交叉污染。为该方法的开发实施了战略实验方法。使用梯度洗脱在Symmetry C18(4.6 X 75 mm,3.5μm)色谱柱上实现所需的色谱分离。优化的流动相由缓冲液四丁基氢氧化铵pH-6.8和乙腈组成。使用光电二极管阵列检测器在215 nm和254 nm波长处监测洗脱的化合物。所开发的方法在50分钟的运行时间内将12-β-内酰胺化合物彼此分离。该方法对于测定青霉素和头孢菌素生产区的交叉污染是有效的。本方法是特定的,并且基于信噪比方法确定了定量的下限。所有成分均为1μg/ mL。根据国际协调会议(ICH)指南验证了开发的RP-HPLC方法。

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