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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Development of a novel analytical method for determination of chondroitin sulfate using an in-capillary enzyme reaction
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Development of a novel analytical method for determination of chondroitin sulfate using an in-capillary enzyme reaction

机译:开发一种利用毛细管内酶反应测定硫酸软骨素的新型分析方法

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A novel analytical method for determination of total amount of chondroitin sulfate (CS) based on its conversion to desulfated chondro-disaccharide via an enzyme-catalyzed reaction, was developed. Using the in-capillary enzyme reaction, the method was also applied to the successful construction of an on-line analytical system. Within this system, electrophoretic migration was used to mix zones containing the enzyme mixture (chondroitinase ABC, chondro-4-sulfatase, chondro-6-sulfatase and 2-o-sulfatase) and the substrate (CS). The reaction was then allowed to proceed in the presence of a weak electric field and, finally, the product (desulfated chondro-disaccharide) of enzyme reaction migrated to the detector under the influence of an applied electric field. A polyvinyl alcohol-coated capillary was used to reduce protein adsorption. Desulfated chondro-disaccharide was successfully migrated toward the anode in 10 MM Tris-acetate buffer (pH 7.0) under reversed polarity and detected at 232 nm. The established method was validated and demonstrated to be applicable in the determination of total amount of CS in a commercial ophthalmic solution. No interference from the formulation excipients was observed. Good linearity was obtained, with correlation coefficients above 0.999. Recoveries and precisions ranged from 100.0 to 100.5%, and from 0.2 to 0.6% of the relative standard deviation, respectively. Good agreement was obtained between the established method and traditional photometric method based on carbazole reaction. In this study, application of the method to disaccharide compositional analysis was also performed. (C) 2004 Elsevier B.V. All rights reserved.
机译:建立了一种新的测定硫酸软骨素(CS)总量的分析方法,该方法是通过酶催化反应转化为脱硫的软骨二糖。使用毛细管内酶反应,该方法也被用于成功构建在线分析系统。在该系统中,电泳迁移用于混合含有酶混合物(软骨素酶ABC,软骨4硫酸软骨素,软骨6硫酸软骨素和2-o硫酸脂酶)和底物(CS)的区域。然后在弱电场的存在下使反应进行,最后,在施加的电场的影响下,酶反应的产物(脱硫酸的软骨二糖)迁移至检测器。使用聚乙烯醇涂层的毛细管可减少蛋白质的吸附。脱硫的软骨二糖在极性相反的10毫米Tris-乙酸盐缓冲液(pH 7.0)中成功迁移到阳极,并在232 nm处检测到。验证了所建立的方法,并证明该方法可用于测定商业眼科溶液中CS的总量。没有观察到制剂赋形剂的干扰。获得了良好的线性,相关系数高于0.999。回收率和精密度分别为相对标准偏差的100.0%至100.5%和0.2%至0.6%。建立的方法与基于咔唑反应的传统光度法之间取得了很好的一致性。在这项研究中,还进行了该方法在二糖成分分析中的应用。 (C)2004 Elsevier B.V.保留所有权利。

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