Department of Mechano-Micro Engineering, Interdisciplinary Graduate School of Science and Engineering, Tokyo Institute of Technology, 4259 Nagatsuta-cho, Midori-ku, Yokohama 226-8503, Japan.
Anal Chim Acta. 2010 Feb 28;661(2):200-5. doi: 10.1016/j.aca.2009.12.022. Epub 2009 Dec 22.
LSPR from nanostructured noble metals such as gold and silver offers great potential for biosensing applications. In this study, a core-shell structured nanoparticle layer substrate was fabricated and the localized surface plasmon resonance (LSPR) optical characteristics were investigated for DNA in aqueous conditions. Factors such as DNA length dependence, concentration dependence, and the monitoring of DNA aspects (ssDNA or dsDNA) were measured. Different lengths and concentrations of DNA solutions were introduced onto the surface of the substrate and the changes in the LSPR optical characteristics were measured. In addition, to monitor the changes in LSPR optical characteristics for different DNA aspects, a DNA solutions denatured by means of heat or alkali were introduced onto the surface, after which optical characterization of the core-shell structured nanoparticle substrate was carried out. With this core-shell structured nanoparticle layer for the excitation of LSPR, the dependence upon specific DNA conditions (length, concentration, and aspect) could be monitored. In particular, the core-shell structured nanoparticle layer substrate could detect DNA of length 100-5000 bp and 400-bp DNA at a concentration of 4.08 ng mL(-1) (1 x 10(7) DNA molecules mL(-1)). Furthermore, the changes in LSPR optical characteristics with DNA aspect could be monitored. Thus, LSPR-based optical detection using a core-shell structured nanoparticle layer substrate can be used to determine the kinetics of biomolecular interactions in a wide range of practical applications such as medicine, drug delivery, and food control.
基于金和银等纳米结构贵金属的局域表面等离子体共振(LSPR)为生物传感应用提供了巨大的潜力。在这项研究中,制备了核壳结构纳米粒子层基底,并研究了其在水相条件下对 DNA 的局域表面等离子体共振(LSPR)光学特性。测量了诸如 DNA 长度依赖性、浓度依赖性以及 DNA 方面(单链 DNA 或双链 DNA)监测等因素。将不同长度和浓度的 DNA 溶液引入到基底表面,并测量 LSPR 光学特性的变化。此外,为了监测不同 DNA 方面的 LSPR 光学特性变化,将通过热或碱变性的 DNA 溶液引入到表面,然后对核壳结构纳米粒子基底进行光学特性分析。通过这种用于激发 LSPR 的核壳结构纳米粒子层,可以监测特定 DNA 条件(长度、浓度和方面)的依赖性。特别是,核壳结构纳米粒子层基底可以检测 100-5000bp 长的 DNA 和 400-bp DNA,浓度为 4.08ngmL(-1)(1 x 10(7)DNA 分子 mL(-1))。此外,还可以监测 DNA 方面的 LSPR 光学特性变化。因此,基于 LSPR 的光学检测可以使用核壳结构纳米粒子层基底来确定广泛的实际应用中的生物分子相互作用动力学,例如医学、药物输送和食品控制。