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以单克隆抗体偶联纳米颗粒作为超顺磁性标记并增强沉降作用的快速一步法全血C反应蛋白磁导率免疫测定法

Rapid one-step whole blood C-reactive protein magnetic permeability immunoassay with monoclonal antibody conjugated nanoparticles as superparamagnetic labels and enhanced sedimentation.

作者信息

Ibraimi Filiz, Kriz Dario, Lu Min, Hansson Lars-Olof, Kriz Kirstin

机构信息

Department of Pure and Applied Biochemistry, Lund University, P.O. Box 124, 221 00, Lund, Sweden.

出版信息

Anal Bioanal Chem. 2006 Feb;384(3):651-7. doi: 10.1007/s00216-005-0094-6. Epub 2005 Oct 21.

DOI:10.1007/s00216-005-0094-6
PMID:16240109
Abstract

A rapid (5.5 min) one-step whole blood C-reactive protein (CRP) magnetic permeability immunoassay utilizing monoclonal antibody conjugated dextran iron oxide nanoparticles (70 nm) as superparamagnetic labels and mixed fractions (1:1 ratio of 15-40 and 60 microm) of polyclonal anti-CRP conjugated silica microparticles for enhanced sedimentation is described. In this one-step assay procedure, a whole blood sample (4 microl) is applied to an assay glass vial, containing both antibody conjugates, and mixed for 30 s. The target analyte, CRP, forms a sandwich complex between the conjugated nanoparticles and microparticles, and, subsequently, the complex sediments under normal gravitation within 5 min to the bottom of the vial. The magnetic permeability increase of the sediment due to the presence of the complexed superparamagnetic nanoparticles is determined using an inductance-based transducer. Assayed patient whole blood samples were compared with the Abbott Diagnostics Architect reference method. A strong linear correlation was observed for the CRP concentration range 0-260 mg/l in whole blood (y=1.001x+0.42, R2=0.982, n=50). The CRP assay presented showed a limit of detection of 3 mg/l and a total imprecision (coefficient of variation) of 10.5%. On the basis of our observations, we propose a rapid, one-step, CRP assay for near-patient testing.

摘要

本文描述了一种快速(5.5分钟)一步法全血C反应蛋白(CRP)磁导率免疫测定法,该方法利用与葡聚糖氧化铁纳米颗粒(70纳米)偶联的单克隆抗体作为超顺磁性标记物,以及多克隆抗CRP偶联二氧化硅微粒的混合级分(15 - 40微米和60微米的1:1比例)来增强沉降。在这个一步法测定程序中,将全血样本(4微升)加入到一个含有两种抗体偶联物的测定玻璃瓶中,并混合30秒。目标分析物CRP在偶联的纳米颗粒和微粒之间形成夹心复合物,随后,该复合物在正常重力作用下5分钟内沉降到瓶底。使用基于电感的传感器测定由于复合超顺磁性纳米颗粒的存在而导致的沉淀物磁导率增加。将测定的患者全血样本与雅培诊断公司的Architect参考方法进行比较。在全血中CRP浓度范围为0 - 260毫克/升时观察到强线性相关性(y = 1.001x + 0.42,R2 = 0.982,n = 50)。所展示的CRP测定法检测限为3毫克/升,总不精密度(变异系数)为10.5%。基于我们的观察结果,我们提出一种用于即时检测的快速一步法CRP测定法。

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