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一种基于荧光各向异性的新型生物传感光学平台。

A new optical platform for biosensing based on fluorescence anisotropy.

作者信息

Baldini F, Carloni A, Giannetti A, Porro G, Trono C

机构信息

Institute of Applied Physics, CNR, Via Madonna del Piano 10, 50019, Sesto Fiorentino (FI), Italy.

出版信息

Anal Bioanal Chem. 2008 Jul;391(5):1837-44. doi: 10.1007/s00216-008-1904-4. Epub 2008 Feb 15.

Abstract

A novel fluorescence-based optical platform for the interrogation of an optical biochip was designed and developed. The optical biochip was made of poly(methyl methacrylate) (PMMA) formed by two pieces of PMMA appropriately shaped in order to obtain four microchannels that are 500-microm wide and 400-microm high. The lower part includes the microchannels and the inlet and outlet for the fluidics, while the sensing biolayer was immobilized on the upper part. The optical signal comprised the fluorescence emitted by the biolayer, which was anisotropically coupled to the PMMA cover and suitably guided by the PMMA chip. The potentiality of the optical chip as a biosensor was investigated by means of a direct IgG/anti-IgG interaction carried out inside the flow channels. The mouse-IgG was covalently immobilized on the internal wall of the PMMA cover, and the Cy5-labelled anti-mouse IgG was used for the specific interaction. Several chemical treatments of the PMMA surface were investigated, poly(L: -lactic acid), Eudragit L100 and NaOH, in order to obtain the most effective distribution of carboxylic groups useful for the covalent immobilisation of the mouse-IgG. The treatment with Eudragit L100 was found to be the most successful. Limits of detection and quantification of 0.05 microg mL(-1) and 0.2 microg mL(-1), respectively, were obtained with the configuration described.

摘要

设计并开发了一种用于检测光学生物芯片的新型荧光光学平台。该光学生物芯片由聚甲基丙烯酸甲酯(PMMA)制成,由两块形状合适的PMMA组成,以获得四个宽500微米、高400微米的微通道。下部包括微通道以及流体的入口和出口,而传感生物层固定在上部。光信号包括生物层发出的荧光,该荧光各向异性地耦合到PMMA盖并由PMMA芯片适当引导。通过在流动通道内进行直接的IgG/抗IgG相互作用,研究了该光芯片作为生物传感器的潜力。将小鼠IgG共价固定在PMMA盖的内壁上,并使用Cy5标记的抗小鼠IgG进行特异性相互作用。研究了PMMA表面的几种化学处理方法,即聚(L-乳酸)、Eudragit L100和NaOH,以获得对小鼠IgG共价固定有用的羧基的最有效分布。发现用Eudragit L100处理是最成功的。采用所述配置分别获得了0.05微克/毫升和0.2微克/毫升的检测限和定量限。

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