Department of Chemical and Biomolecular Engineering, Yonsei University, 134 Sinchon-Dong, Seodaemoon-Gu, Seoul, 120-749, Republic of Korea.
Analyst. 2010 Nov;135(11):2871-8. doi: 10.1039/c0an00353k. Epub 2010 Sep 20.
This paper describes the use of microarray-based biosensor system for the determination of phenol. Microarrays based on poly(ethylene glycol)(PEG) hydrogel were prepared by photopatterning of a solution containing PEG diacrylate (PEG-DA), photoinitiator, tyrosinase, and CdSe/ZnS quantum dots (QDs). During photo-induced crosslinking, tyrosinase and QDs were entrapped within the hydrogel microarrays, making the hydrogel microarray fluorescent and responsive to phenol. The entrapped tyrosinase could carry out enzyme-catalyzed oxidation of phenol to produce quinones, which subsequently quenched the fluorescence of QDs within hydrogel microarray. The fluorescence intensity of the hydrogel microarrays decreased linearly according to phenol concentration and the detection limit of this system was found to be 1.0 μM. The microarray system presented in this study could be combined with a microfluidic device as an initial step to create a phenol-detecting "micro-total-analysis-system (μ-TAS)".
本文介绍了基于微阵列生物传感器系统用于测定苯酚。通过光聚合含有聚乙二醇二丙烯酸酯(PEG-DA)、光引发剂、酪氨酸酶和CdSe/ZnS 量子点(QDs)的溶液制备基于聚乙二醇(PEG)水凝胶的微阵列。在光诱导交联过程中,酪氨酸酶和 QDs 被包埋在水凝胶微阵列中,使水凝胶微阵列具有荧光性并对苯酚有响应。包埋的酪氨酸酶可以进行酶催化氧化苯酚生成醌,随后猝灭水凝胶微阵列中 QDs 的荧光。水凝胶微阵列的荧光强度根据苯酚浓度呈线性降低,该系统的检测限被发现为 1.0 μM。本研究中提出的微阵列系统可以与微流控装置结合,作为创建苯酚检测的“微全分析系统(μ-TAS)”的初始步骤。