College of Chemistry, Jilin University, Changchun 130012, PR China.
Colloids Surf B Biointerfaces. 2010 Nov 1;81(1):249-54. doi: 10.1016/j.colsurfb.2010.07.014. Epub 2010 Jul 13.
A resonance light scattering (RLS) spectrometry for determining DNA based on localized surface plasmon resonance (LSPR) of gold nanorods was developed. The fabrication and characterization of the biosensor utilized gold nanorods as the optical transducer was described. The DNA was determined based on the binding of DNA to gold nanorods by electrostatic adsorption. The RLS intensity of the gold nanorods was enhanced in the presence of DNA. The peaks of the enhanced RLS spectrum were at the wavelength 311 and 581 nm. The binding of DNA to the gold nanorods causes an increase of the RLS intensity that is responsive to the concentration of DNA. Under the optimal conditions, the enhanced RLS intensities are directly proportional to the DNA concentrations in the range of 0.05-0.5 microg/mL. The proposed method was successfully applied to the determination of DNA in the samples and the results were satisfactory.
基于金纳米棒的局域表面等离子体共振(LSPR)的共振光散射(RLS)光谱法用于测定 DNA。描述了利用金纳米棒作为光学换能器的生物传感器的制备和表征。DNA 的测定是基于 DNA 通过静电吸附与金纳米棒的结合。在存在 DNA 的情况下,金纳米棒的 RLS 强度增强。增强的 RLS 光谱的峰值位于波长 311 和 581nm 处。DNA 与金纳米棒的结合导致 RLS 强度的增加,这与 DNA 的浓度呈响应关系。在最佳条件下,增强的 RLS 强度与 0.05-0.5μg/mL 范围内的 DNA 浓度呈正比。该方法成功地应用于样品中 DNA 的测定,结果令人满意。