Lanz Christian, Kuhn Martina, Deiss Veronika, Thormann Wolfgang
Department of Clinical Pharmacology, University of Bern, Bern, Switzerland.
Electrophoresis. 2004 Jul;25(14):2309-18. doi: 10.1002/elps.200305859.
Capillary zone electrophoresis (CZE) with a dynamic double coating formed by charged polymeric reagents represents an effective tool for the separation of iron-saturated transferrin (Tf) isoforms and thus the determination of carbohydrate-deficient transferrin (CDT, sum of asialo-, monosialo- and disialo-Tf in relation to total Tf) in human serum. Using the CEofix-CDT reagents, a 50 microm inner diameter (ID) capillary of 60 cm total length and the P/ACE MDQ under optimized instrumental conditions (20 kV and 30 degrees C) is demonstrated to provide outstanding assay precision for the determination of CDT in human serum. For CDT levels of 1.0% and 4.5%, precision relative standard deviation (RSD) values (n = 8) were determined to be < 3.0% and < 1.5%, respectively. During the first year of operation under routine conditions, more than 600 patient samples were analyzed in a total of 62 sets of runs. Except for selected samples of patients with severe liver diseases, interference-free Tf patterns were detected. Asialo-Tf was not detected in control sera and in patient sera with a CDT level < 1.70%, but became detectable in 89.6% of sera with > 2.3% disialo-Tf. Monosialo-Tf was only detected in two sera containing > 13.3% CDT. The optimized CZE assay was applied to confirm positive CDT results produced by an immunoassay during long-term monitoring of a patient which led to the determination of the elimination kinetics of asialo-Tf, disialo-Tf, and CDT after an episode of high alcohol consumption (estimated apparent half lifes of 4.86, 7.24, and 6.74 days, respectively). The optimized CZE assay with an upper reference limit for CDT of 1.70% represents an attractive alternative to high-performance liquid chromatography (HPLC). It features simpler sample preparation, faster analysis time, and higher isoform resolution compared to the most recent HPLC approach and can thus be regarded as a new candidate of a reference method for CDT.
采用带电聚合试剂形成动态双涂层的毛细管区带电泳(CZE)是分离铁饱和转铁蛋白(Tf)异构体以及测定人血清中缺糖转铁蛋白(CDT,即去唾液酸转铁蛋白、单唾液酸转铁蛋白和双唾液酸转铁蛋白之和与总Tf的比值)的有效工具。使用CEofix - CDT试剂,内径50微米、总长60厘米的毛细管以及P/ACE MDQ,在优化的仪器条件(20 kV和30℃)下,已证明可为人血清中CDT的测定提供出色的分析精密度。对于CDT水平为1.0%和4.5%的情况,相对标准偏差(RSD)值(n = 8)分别确定为< 3.0%和< 1.5%。在常规条件下运行的第一年,共62组运行中分析了600多个患者样本。除了患有严重肝脏疾病患者的选定样本外,均检测到无干扰的Tf模式。在对照血清和CDT水平< 1.70%的患者血清中未检测到去唾液酸转铁蛋白,但在双唾液酸转铁蛋白> 2.3%的血清中89.6%可检测到。单唾液酸转铁蛋白仅在两份CDT含量> 13.3%的血清中检测到。优化后的CZE测定法用于确认免疫测定法在对一名患者进行长期监测期间产生的CDT阳性结果,并由此确定了一次高酒精摄入量发作后去唾液酸转铁蛋白、双唾液酸转铁蛋白和CDT的消除动力学(估计表观半衰期分别为4.86、7.24和6.74天)。CDT上限参考值为1.70%的优化CZE测定法是高效液相色谱(HPLC)的一种有吸引力的替代方法。与最新的HPLC方法相比,它具有更简单的样品制备、更快的分析时间和更高的异构体分辨率,因此可被视为CDT参考方法的新候选者。