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利用免疫磁珠的顺序注射免疫测定法。

Sequential injection immunoassay utilizing immunomagnetic beads.

作者信息

Pollema C H, Ruzicka J, Christian G D, Lernmark A

机构信息

Department of Chemistry, University of Washington, Seattle 98195.

出版信息

Anal Chem. 1992 Jul 1;64(13):1356-61. doi: 10.1021/ac00037a010.

Abstract

A novel sequential injection immunoassay (SIIA) method is described which utilizes immunomagnetic beads to investigate short-time antibody binding. The method is versatile and flexible and may therefore be adapted to many different applications. Initial results for a competitive assay are also presented. The immunomagnetic bead reactor is created within the flowing stream by retaining immunomagnetic beads with an electromagnet to form an open tube reactor. Thus, the spent beads may be discharged after each analysis. This eliminates the problems of instability of reaction surfaces and eliminates the need for additional time traditionally required for regeneration of the solid-reacting phase in order to not only save time and increase sampling frequency but also to provide each individual sampling cycle with a fresh, uniform portion of beads. The spent beads are collected off line and may be regenerated later. Short-time binding kinetic studies demonstrate linear initial binding under 1 min, which then begins to reach saturation in approximately 10 min. Competitive binding assays of monoclonal mouse IgG (MRC OX-19) to polyclonal sheep anti-mouse IgG immobilized to the immunomagnetic beads show reproducible linear displacement in 30-120-s reactions. Fluorescence detection is utilized with a detection limit of 155 ng/mL, and since the reaction time is typically 2 min or shorter, the sampling frequency is 30 samples/h.

摘要

本文描述了一种新型的顺序注射免疫分析(SIIA)方法,该方法利用免疫磁珠研究短时间内的抗体结合情况。该方法具有通用性和灵活性,因此可适用于许多不同的应用。文中还给出了竞争分析的初步结果。通过用电磁铁保留免疫磁珠在流动流中形成一个开放管式反应器,从而创建免疫磁珠反应器。这样,每次分析后用过的磁珠可以排出。这消除了反应表面不稳定的问题,也消除了传统上固体反应相再生所需的额外时间,不仅节省了时间并提高了采样频率,还为每个单独的采样周期提供了新鲜、均匀的磁珠部分。用过的磁珠离线收集,之后可以再生。短时间结合动力学研究表明,在1分钟内初始结合呈线性,然后在大约10分钟时开始达到饱和。单克隆小鼠IgG(MRC OX - 19)与固定在免疫磁珠上的多克隆羊抗小鼠IgG的竞争结合分析在30 - 120秒的反应中显示出可重复的线性位移。采用荧光检测,检测限为155 ng/mL,由于反应时间通常为2分钟或更短,采样频率为每小时30个样品。

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