Development and validation of transient isotachophoretic capillary zone electrophoresis for determination of peptides

被引:17
|
作者
Waterval, JCM [1 ]
la Porte, CJL [1 ]
van't Hof, R [1 ]
Teeuwsen, J [1 ]
Bult, A [1 ]
Lingeman, H [1 ]
Underberg, WJM [1 ]
机构
[1] Univ Utrecht, Fac Pharm, Dept Pharmaceut Anal, NL-3508 TB Utrecht, Netherlands
关键词
transient isotachophoresis; stacking; peptides;
D O I
10.1002/elps.1150191820
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Although capillary zone electrophoresis (CZE) is known for its high resolution power and low mass detection limits, the concentration detection limits are rather poor when ultraviolet absorbance detection is used. To overcome this limitation, several on-column transient isotachophoresis (tITP) protocols have been developed and validated for the determination of both cationic and anionic model peptides, separately. Using this preconcentration method, up to 72% of the capillary can be filled with sample solution, without any loss in resolution. Thus, without any modification of the hardware set-up, the sensitivity is increased about two orders of magnitude. For the model cationic peptides (gonadorelin, angiotensin II) good linearity and reproducibility is observed in the 20 to 100 ng/mL concentration range. For the anionic peptides (N-t-Boc-Pentagastrin and two related peptides), a tITP method was developed using a dynamically coated capillary. The coating was prepared by adding Fluorad FC-135(R) to the leading electrolyte buffer. In this way a positively charged bilayer was formed on the inside of the capillary, producing an electroosmotic flow towards the outlet using reversed polarity conditions. In this way, acceptable analysis times were achieved. Using the developed tITP method, up to 72% of the capillary can be filled with sample solution as well. The anionic peptides are separated even better than when using CZE conditions. Linearity and reproducibility in the 20-100 ng/mL range proved to be excellent.
引用
收藏
页码:3171 / 3177
页数:7
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