Stroink Thom, Schravendijk Pim, Wiese Gerard, Teeuwsen Jan, Lingeman Henk, Waterval Joop C M, Bult Auke, de Jong Gerhardus J, Underberg Willy J M
Department of Biomedical Analysis, Faculty of Pharmaceutical Sciences, Utrecht University, Utrecht, The Netherlands.
Electrophoresis. 2003 Mar;24(6):1126-34. doi: 10.1002/elps.200390132.
Since biologically active peptides usually exhibit their effects in low concentrations, the development of sensitive analytical methods has become a challenge. In this paper, a multidimensional system is presented, consisting of a size-exclusion chromatographic (SEC) separation followed by a trapping procedure on a 4 mm x 3 mm ID reversed-phase C18 (RP18) column with subsequent elution of the trapped fraction and separation by capillary zone electrophoresis (CZE). The system has been tested with mixtures of six enkephalins and albumin, mimicking biological matrices such as plasma and cerebrospinal fluid. After separation of albumin from the enkephalins in the SEC dimension a heart-cut of 200 micro L, containing the enkephalin peak, is taken, concentrated on the RP18 microcolumn and, after elution with a 20 micro L plug of 80% acetonitrile, electrokinetically injected into the CZE system, where stacking and separation is achieved. While validation shows generally good linearity and reproducibility, the quantitation limit with UV detection is acceptable (2.5 micro g/ mL with an injection volume of 50 micro L).
由于生物活性肽通常在低浓度下发挥作用,因此开发灵敏的分析方法成为一项挑战。本文介绍了一种多维系统,该系统由尺寸排阻色谱(SEC)分离、在内径4 mm×3 mm的反相C18(RP18)柱上进行捕集步骤、随后洗脱捕集的馏分并通过毛细管区带电泳(CZE)分离组成。该系统已用六种脑啡肽和白蛋白的混合物进行了测试,模拟了血浆和脑脊液等生物基质。在SEC维度中从脑啡肽中分离出白蛋白后,取200微升包含脑啡肽峰的中心切割馏分,浓缩在RP18微柱上,并用20微升80%乙腈塞洗脱后,电动注入CZE系统,在该系统中实现堆积和分离。虽然验证显示总体线性和重现性良好,但紫外检测的定量限是可接受的(进样体积50微升时为2.5微克/毫升)。