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基于硅基胶体晶体微球的新型化学发光免疫分析用于多重肿瘤标志物检测。

Multiplex tumor marker detection with new chemiluminescent immunoassay based on silica colloidal crystal beads.

机构信息

Department of Hematology, Affiliated Zhongda Hospital, School of Clinical Medicine, Southeast University, Nanjing 210009, China.

出版信息

Analyst. 2010 Jan;135(1):177-81. doi: 10.1039/b912880h. Epub 2009 Nov 13.

Abstract

A new multiplex chemiluminescent immunoassay (CLIA) based on silica colloidal crystal beads (SCCBs) was developed for tumor marker detection. As the code is the characteristic reflection peak originating from the stop-band of colloid crystal, they avoid photobleaching, the potential interference of encoding fluorescence with analyte-detection fluorescence and chemical instability. Meanwhile our SCCBs suspension array improved the luminescence analysis efficiency by using chemiluminescent detection of enzyme labels. By forming a sandwich immunocomplex on SCCBs, the proposed suspension array was used for simultaneous multiplex detection of tumor markers in one test tube. The results showed that the linear range was 0.5-100ng ml(-1) and 1.0-120ng ml(-1) for carcinoembryonic antigen (CEA) and alpha-fetoprotein (AFP) with a detection limit of 0.12ng ml(-1) and 0.16ng ml(-1) at 3sigma. The proposed array showed the storage stability and the accuracy for sample detection were acceptable, and the results were in acceptable agreement with the reference electrochemiluminescence method. This technique provided an automated, simple, sensitive and low-cost approach for multianalyte immunoassay.

摘要

一种新的基于硅胶胶体晶体珠(SCCBs)的多重化学发光免疫分析(CLIA)被开发用于肿瘤标志物检测。由于代码是源于胶体晶体的停止带的特征反射峰,它们避免了光漂白、编码荧光与分析物检测荧光的潜在干扰和化学不稳定性。同时,我们的 SCCBs 悬浮阵列通过使用酶标记物的化学发光检测提高了发光分析效率。通过在 SCCBs 上形成夹心免疫复合物,该悬浮阵列用于在一个试管中同时多重检测肿瘤标志物。结果表明,CEA 和 AFP 的线性范围分别为 0.5-100ng ml(-1)和 1.0-120ng ml(-1),检测限分别为 0.12ng ml(-1)和 0.16ng ml(-1),在 3sigma 处。该阵列表现出可接受的储存稳定性和样品检测的准确性,并且结果与参考电化学发光法具有可接受的一致性。该技术为多分析物免疫分析提供了一种自动化、简单、灵敏和低成本的方法。

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