Capillary electrophoretic determination of acetic acid and trifluoroacetic acid in synthetic peptide samples

被引:14
作者
Hettiarachchi, K [1 ]
Ridge, S [1 ]
机构
[1] SRI Int, Dept Analyt Chem, Biopharmaceut Dev Div, Menlo Park, CA 94025 USA
关键词
acetic acid; trifluoroacetic acid; peptides; opioid peptides; TIPP[psi; orphanin FQ; glutamic acid;
D O I
10.1016/S0021-9673(98)00328-8
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Synthetic peptide samples may contain counter-ions such as acetate or trifluoroacetate as a result of their method of preparation. Furthermore, because acetic acid (HOAc) and trifluoroacetic acid (TFA) are frequently used reagents in peptide synthesis, these acids may be found in synthetic peptide samples as impurities. This paper describes a method validation to determine HOAc and TFA in synthetic peptide samples by capillary electrophoresis (CE) using an internal standard (I.S.) with indirect UV detection. Typical analytical parameters such as precision, linearity, accuracy, specificity, limit of detection and ruggedness were evaluated during the validation. In addition, the contents of HOAc and TFA in two synthetic opioid peptide samples, TIPP[psi] and Orphanin FQ, were determined using the validated method. A unique feature of the method is that it offers determination of both acids in a single assay using a common I.S. The method is very efficient because of relatively short electrophoretic migration times (typically 2 to 8 min) for the acids investigated. This paper also discusses the factors that affect precision in a CE assay. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:153 / 161
页数:9
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