Hacettepe University, Department of Chemistry, Ankara, Turkey.
Biosens Bioelectron. 2010 Oct 15;26(2):815-21. doi: 10.1016/j.bios.2010.06.003. Epub 2010 Jun 11.
The aim of this study is to prepare quartz crystal microbalance (QCM) nanosensor for the real-time detection of lysozyme. In the first part, the lysozyme imprinted (MIP) nanoparticles were prepared by mini-emulsion polymerization. The MIP nanoparticles were characterized by TEM, zeta-sizer and FTIR-ATR measurements. Particle size was found around 50 nm. The MIP nanoparticles were attached by dropping of nanoparticle solution to gold surface and then, dried at 37°C for 6h. QCM nanosensor was characterized with AFM and ellipsometer. The observations indicated that the nanoparticle film was almost monolayer. The detection limit was found as 1.2 ng/mL. The specificity of the QCM nanosensor was shown by using albumin as a competitor molecule. The results show that the QCM nanosensor has high selectivity and sensitivity with a wide range of lysozyme concentrations in both aqueous solutions (0.2-1500 μg/mL) and natural sources (egg white) (460-1500 ng/mL).
本研究旨在制备石英晶体微天平(QCM)纳米传感器,用于实时检测溶菌酶。在第一部分中,通过细乳液聚合制备了溶菌酶印迹(MIP)纳米粒子。通过 TEM、zeta 粒径仪和 FTIR-ATR 测量对 MIP 纳米粒子进行了表征。粒径约为 50nm。通过将纳米粒子溶液滴加到金表面并在 37°C 下干燥 6h 将 MIP 纳米粒子附着。用 AFM 和椭偏仪对 QCM 纳米传感器进行了表征。观察表明,纳米粒子膜几乎为单层。检测限为 1.2ng/mL。通过使用白蛋白作为竞争分子,证明了 QCM 纳米传感器具有高选择性和灵敏度,可检测水溶液(0.2-1500μg/mL)和天然来源(蛋清)(460-1500ng/mL)中广泛的溶菌酶浓度。