Spadavecchia J, Prete P, Lovergine N, Tapfer L, Rella R
Instituto per la Microelettronica e i Microsistemi (IMM-CNR), Sezione di Lecce, Via Arnesano, I-73100 Lecce, Italy.
J Phys Chem B. 2005 Sep 22;109(37):17347-9. doi: 10.1021/jp053194j.
Gold nanoparticles heavily functionalized with oligonucleotides have been used in a variety of DNA detection methods. The optical properties of three-dimensional aggregates of Au nanoparticles in solution or deposited onto suitable surfaces have been analyzed to detect hybridization processes of specific DNA sequences as possible alternatives to fluorescent labeling methods. This paper reports on the preparation of gold nanoparticles directly deposited onto the surface of silicon (Si) and sapphire (Al2O3) substrates by a physical methodology, consisting in the thermal evaporation of a thin Au film and its successive annealing. The method guarantees the preparation of monodispersed single-crystal Au nanoparticles with a strong surface plasmon resonance (SPR) peak centered at about 540 nm. We show that the changes of SPR excitation before and after DNA functionalization and subsequent hybridization of Au nanoparticles immobilized onto Si and Al2O3 substrates can be exploited to fabricate specific biosensors devices in solid phase.
用寡核苷酸高度功能化的金纳米颗粒已被用于多种DNA检测方法中。溶液中或沉积在合适表面上的金纳米颗粒三维聚集体的光学性质已被分析,以检测特定DNA序列的杂交过程,作为荧光标记方法的可能替代方案。本文报道了通过一种物理方法直接将金纳米颗粒沉积在硅(Si)和蓝宝石(Al2O3)衬底表面的制备方法,该方法包括热蒸发薄金膜及其后续退火。该方法保证了制备出具有以约540nm为中心的强表面等离子体共振(SPR)峰的单分散单晶金纳米颗粒。我们表明,固定在Si和Al2O3衬底上的金纳米颗粒在DNA功能化和随后杂交前后的SPR激发变化可用于制造固相特异性生物传感器装置。