Ma Qiang, Wang Xinyan, Li Yabing, Su Xingguang, Jin Qinhan
Department of Analytical Chemistry, College of Chemistry, Jilin University, Changchun 130012, People's Republic of China.
Luminescence. 2007 Sep-Oct;22(5):438-45. doi: 10.1002/bio.982.
Polystyrene fluorescent microspheres prepared by deposition of CdTe quantum dots (QDs) are used in an immunoassay in this study. CdTe QDs/polyelectrolyte multilayers on the surface of polystyrene microspheres have been formed by layer-by-layer self-assembly via electrostatic interactions. As a model antigen, rabbit IgG has been bound to the outermost layer of the fluorescent microspheres. The immunoreaction between fluorescent microspheres/rabbit IgG and the corresponding antibody was confirmed by change of the fluorescence spectrum and competitive immunoassay. This approach allowed detection of the antigen (rabbit IgG) in the range 1-500 mg/L, based on the change in the fluorescence intensity of the reporter (fluorescent microspheres/rabbit IgG). A novel microfluidic chip device with a laser-induced fluorescence system was established and used for the detection of fluorescent microspheres in this study.
本研究中,通过沉积碲化镉量子点(QDs)制备的聚苯乙烯荧光微球被用于免疫测定。聚苯乙烯微球表面的碲化镉量子点/聚电解质多层膜通过静电相互作用逐层自组装形成。作为模型抗原,兔免疫球蛋白G(IgG)已结合到荧光微球的最外层。荧光微球/兔IgG与相应抗体之间的免疫反应通过荧光光谱变化和竞争性免疫测定得以证实。基于报告物(荧光微球/兔IgG)荧光强度的变化,该方法能够检测浓度范围为1至500 mg/L的抗原(兔IgG)。本研究中建立了一种带有激光诱导荧光系统的新型微流控芯片装置,并用于检测荧光微球。