Article ID Journal Published Year Pages File Type
1224559 Journal of Pharmaceutical and Biomedical Analysis 2006 7 Pages PDF
Abstract

A method using reversed-phase high performance liquid chromatography (HPLC) with UV detection has been developed and validated for the trace level (ng/mL) detection and quantitation of ethyl diazoacetate (EDA), a toxic impurity, in sample matrix. Method development included the evaluation of several analytical techniques including LC–MS and GC–MS, which in this case, proved to be unacceptable means of analysis. The chromatographic separation employed in this method utilizes a mobile phase system of acetonitrile and water with analysis carried out using UV detection at 250 nm. The final method showed excellent linearity, accuracy, repeatability, specificity and recovery when evaluated at the quantitation limit (QL) of 6 ng/mL.

Related Topics
Physical Sciences and Engineering Chemistry Analytical Chemistry
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