Department of Chemical and Materials Engineering, National University of Kaohsiung, Kaohsiung 811, Taiwan.
Biosens Bioelectron. 2009 Nov 15;25(3):579-86. doi: 10.1016/j.bios.2009.03.039. Epub 2009 Apr 2.
The high stability of quantum dots (QDots) with photoluminescence has led to their increased use as imaging approaches in biological systems to replace conventional fluorescence labels. The antibodies are generally coated on the surface of QDots to the targeting site, and molecular imprinting polymers are designed to mimic the antibodies. Hence, quantum dots can be incorporated into molecularly imprinted polymers, which provide shape and selectivity, and then respond to template rebinding by emitting quenched photoluminescence. In this study, poly(ethylene-co-ethylene alcohol) creatinine-, albumin- and lysozyme-imprinted polymers nanoparticles are synthesized via phase inversion of poly(ethylene-co-ethylene alcohol) with various ethylene mole ratios when target molecules and hydrophobic quantum dots are mixed within the polymer solution. Finally, those particles were prepared for the detection of creatinine, human serum albumin and lysozyme in real sample (urine) and compared with commercial ARCHITECT ci 8200 system.
量子点(QDots)具有高光稳定性,因此在生物系统中作为成像方法的应用越来越多,以取代传统的荧光标记。抗体通常被涂覆在量子点的表面上以靶向特定位置,而分子印迹聚合物则被设计用来模拟抗体。因此,量子点可以被纳入分子印迹聚合物中,这些聚合物提供形状和选择性,然后通过发出猝灭的光致发光来响应模板的再结合。在这项研究中,通过在聚合物溶液中混合目标分子和疏水性量子点,合成了具有不同乙烯摩尔比的聚(乙烯-共-乙二醇)肌酐、白蛋白和溶菌酶印迹聚合物纳米粒子。最后,这些粒子被制备用于检测真实样本(尿液)中的肌酐、人血清白蛋白和溶菌酶,并与商业 ARCHITECT ci 8200 系统进行了比较。