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基于顺序注射-酶联免疫吸附测定的在线透明质酸测定系统。

Sequential injection-ELISA based system for online determination of hyaluronan.

作者信息

Hartwell Supaporn Kradtap, Srisawang Boonraksa, Kongtawelert Prachya, Jakmunee Jaroon, Grudpan Kate

机构信息

Department of Chemistry, Faculty of Science, Chiang Mai University, Chiang Mai, Thailand.

出版信息

Talanta. 2005 Apr 15;66(2):521-7. doi: 10.1016/j.talanta.2004.11.032. Epub 2005 Jan 4.

Abstract

Sequential injection-bead-based immunoassay system has been developed. The main purpose is to make immunoassay process more automated by manipulating the precise delivery of micro-volumes of reagents and the precise timing of incubation and washing steps with a computer program that controls the bi-directional syringe pump. The manifold was designed with the aims of reducing back pressure from beads that act as solid surfaces for immobilization of the target substance, reducing dispersion and dilution of the reagent during incubation, and maximizing signal while minimizing incubation time. This was done by introducing air segment to separate the reagent zone from the carrier stream and by using a suitable sensitive detector which, in this case, was an amperometer. In this study, hyaluronan (HA) was used as a target analyte because of its clinical significance as a potential biomarker for liver, bone and cancer diseases. Amount of hyaluronan was determined using competitive enzyme linked immuno sorbent assay (ELISA) based technique where immobilized HA and HA in solution compete to bind with a fixed amount of biotinylated HA-binding proteins (b-HABPs). Upon separation of the two phases, anti-biotin conjugated with enzyme and a suitable substrate were introduced to follow the binding reaction of the immobilized HA and b-HABPs whose degree of binding is indirectly proportional to the amount of HA in solution. A calibration curve was constructed from a series of concentrations of HA standards. Lowest detectable concentration was found to be 1 ng/mL with the dynamic working range of 1-5000 ng/mL and R.S.D. of intra-assay (n=7) and inter-assay (n=3) of various HA concentrations were 4-10% and 9-12%, respectively. Used beads could be reused by washing with 2M guanidine. Total analysis time for this automatic assay was about 30 min as compared to the 5-8h used in conventional batch well ELISA. The system could be applied to assay HA in human serum.

摘要

已开发出基于顺序注射珠的免疫分析系统。其主要目的是通过计算机程序控制双向注射泵来精确输送微升体积的试剂,并精确控制孵育和洗涤步骤的时间,从而使免疫分析过程更加自动化。流路的设计旨在降低作为固定目标物质的固体表面的珠子产生的背压,减少孵育过程中试剂的分散和稀释,并在最短孵育时间的同时最大化信号。这是通过引入空气段将试剂区与载流分开,并使用合适的灵敏检测器(在本研究中为安培计)来实现的。在本研究中,透明质酸(HA)被用作目标分析物,因为它作为肝脏、骨骼和癌症疾病的潜在生物标志物具有临床意义。使用基于竞争酶联免疫吸附测定(ELISA)的技术测定透明质酸的量,其中固定化的HA和溶液中的HA竞争与固定量的生物素化HA结合蛋白(b-HABP)结合。两相分离后,引入与酶偶联的抗生物素和合适的底物,以跟踪固定化的HA和b-HABP的结合反应,其结合程度与溶液中HA的量成反比。根据一系列HA标准浓度构建校准曲线。最低检测浓度为1 ng/mL,动态工作范围为1-5000 ng/mL,不同HA浓度的批内精密度(n=7)和批间精密度(n=3)的相对标准偏差分别为4-10%和9-12%。用过的珠子可用2M胍洗涤后重复使用。与传统批量孔ELISA使用的5-8小时相比,这种自动分析的总分析时间约为30分钟。该系统可应用于人血清中HA的检测。

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