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药物分子的电聚合分子印迹聚合物(E-MIP)SPR 传感:预聚合的三联噻吩和咔唑电活性单体复合物。

Electropolymerization molecularly imprinted polymer (E-MIP) SPR sensing of drug molecules: pre-polymerization complexed terthiophene and carbazole electroactive monomers.

机构信息

Department of Chemistry, University of Houston, Houston, TX 77204-5003, United States.

出版信息

Biosens Bioelectron. 2011 Jan 15;26(5):2766-71. doi: 10.1016/j.bios.2010.10.027. Epub 2010 Oct 21.

Abstract

A novel chemosensitive ultrathin film with high selectivity was developed for the detection of naproxen, paracetamol, and theophylline using non-covalent electropolymerized molecular imprinted polymers (E-MIP). A series of monofunctional and bifunctional H-bonding terthiophene and carbazole monomers were compared for imprinting these drugs without the use of a separate cross-linker. A key step is the fast and efficient potentiostatic method of washing the template, which facilitated enhanced real-time sensing by surface plasmon resonance (SPR) spectroscopy. Various surface characterizations (contact angle, ellipsometry, XPS, AFM) of the E-MIP film verified the templating and release of the drug from the cross-linked conducting polymer film.

摘要

开发了一种具有高选择性的新型化学敏感超薄膜,用于使用非共价电化学聚合分子印迹聚合物(E-MIP)检测萘普生、对乙酰氨基酚和茶碱。比较了一系列单官能和双官能氢键三噻吩和咔唑单体,用于印迹这些药物,而无需使用单独的交联剂。关键步骤是模板的快速高效的恒电位清洗方法,这通过表面等离子体共振(SPR)光谱学促进了增强的实时传感。E-MIP 薄膜的各种表面特性(接触角、椭圆光度法、XPS、AFM)验证了药物从交联导电聚合物薄膜中的模板化和释放。

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