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通过电活性和表面活性嵌段共聚物功能化制备生物活性表面

Fabrication of Bioactive Surfaces by Functionalization of Electroactive and Surface-Active Block Copolymers.

作者信息

Olubi Omotunde, London Laurisa, Sannigrahi Biswajit, Nagappan Peri, Williams Michael, Khan Ishrat M

机构信息

Center for Functional Nanoscale Materials and Department of Chemistry, Clark Atlanta University, Atlanta, GA 30314, USA.

Center for Cancer Research and Therapeutic Development, Clark Atlanta University, Atlanta, GA 30314, USA.

出版信息

Bioengineering (Basel). 2014 Aug 20;1(3):134-153. doi: 10.3390/bioengineering1030134.

Abstract

Biofunctional block copolymers are becoming increasingly attractive materials as active components in biosensors and other nanoscale electronic devices. We have described two different classes of block copolymers with biofuctional properties. Biofunctionality for block copolymers is achieved through functionalization with appropriate biospecific ligands. We have synthesized block copolymers of electroactive poly(3-decylthiophene) and 2-hydroxyethyl methacrylate by atom transfer radical polymerization. The block copolymers were functionalized with the dinitrophenyl (DNP) groups, which are capable of binding to Immunoglobulin E (IgE) on cell surfaces. The block copolymers were shown to be redox active. Additionally, the triblock copolymer of α, ω-bi-biotin (poly(ethylene oxide)-b-poly (styrene)-b-poly(ethylene oxide)) was also synthesized to study their capacity to bind fluorescently tagged avidin. The surface-active property of the poly(ethylene oxide) block improved the availability of the biotin functional groups on the polymer surfaces. Fluorescence microscopy observations confirm the specific binding of biotin with avidin.

摘要

生物功能嵌段共聚物作为生物传感器和其他纳米级电子设备中的活性成分,正成为越来越有吸引力的材料。我们已经描述了两类具有生物功能特性的嵌段共聚物。嵌段共聚物的生物功能是通过用适当的生物特异性配体进行功能化来实现的。我们通过原子转移自由基聚合合成了电活性聚(3 - 癸基噻吩)和甲基丙烯酸2 - 羟乙酯的嵌段共聚物。这些嵌段共聚物用二硝基苯基(DNP)基团进行功能化,该基团能够与细胞表面的免疫球蛋白E(IgE)结合。这些嵌段共聚物显示出氧化还原活性。此外,还合成了α,ω - 双生物素的三嵌段共聚物(聚(环氧乙烷)-b - 聚(苯乙烯)-b - 聚(环氧乙烷)),以研究它们结合荧光标记抗生物素蛋白的能力。聚(环氧乙烷)嵌段的表面活性特性提高了聚合物表面生物素官能团的可用性。荧光显微镜观察证实了生物素与抗生物素蛋白的特异性结合。

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