Addae Sarah A, Pinard Melissa A, Caglayan Humeyra, Cakmakyapan Semih, Caliskan Deniz, Ozbay Ekmel, Aslan Kadir
Morgan State University, Department of Chemistry, Baltimore, MD, 21251, USA.
Nano Biomed Eng. 2010 Jan 1;2(3):155-164. doi: 10.5101/nbe.v2i3.p155-164.
We report a new approach to colorimetric Enzyme-Linked Immunosorbent Assay (ELISA) that reduces the total assay time to < 2 min and the lower-detection-limit by 100-fold based on absorbance readout. The new approach combines the use of silver nanoparticles, microwaves and split ring resonators (SRR). The SRR structure is comprised of a square frame of copper thin film (30 µm thick, 1 mm wide, overall length of ~9.4 mm on each side) with a single split on one side, which was deposited onto a circuit board (2×2 cm(2)). A single micro-cuvette (10 µl volume capacity) was placed in the split of the SRR structures. Theoretical simulations predict that electric fields are focused in and above the micro-cuvette without the accumulation of electrical charge that breaks down the copper film. Subsequently, the walls and the bottom of the micro-cuvette were coated with silver nanoparticles using a modified Tollen's reaction scheme. The silver nanoparticles served as a mediator for the creation of thermal gradient between the bioassay medium and the silver surface, where the bioassay is constructed. Upon exposure to low power microwave heating, the bioassay medium in the micro-cuvette was rapidly and uniformly heated by the focused electric fields. In addition, the creation of thermal gradient resulted in the rapid assembly of the proteins on the surface of silver nanoparticles without denaturing the proteins. The proof-of-principle of the new approach to ELISA was demonstrated for the detection of a model protein (biotinylated-bovine serum albumin, b-BSA). In this regard, the detection of b-BSA with bulk concentrations (1 µM to 1 pM) was carried out on commercially available 96-well high throughput screening (HTS) plates and silver nanoparticle-deposited SRR structures at room temperature and with microwave heating, respectively. While the room temperature bioassay (without microwave heating) took 70 min to complete, the identical bioassay took < 2 min to complete using the SRR structures (with microwave heating). A lower detection limit of 0.01 nM for b-BSA (100-fold lower than room temperature ELISA) was observed using the SRR structures.
我们报告了一种比色酶联免疫吸附测定(ELISA)的新方法,该方法基于吸光度读数,将总测定时间缩短至<2分钟,并将检测下限降低了100倍。新方法结合了银纳米颗粒、微波和裂环谐振器(SRR)的使用。SRR结构由一侧有单缝的铜薄膜方框架(厚30μm,宽1mm,每边总长约9.4mm)组成,该框架沉积在电路板(2×2 cm(2))上。将单个微型比色皿(体积容量为10μl)放置在SRR结构的缝隙中。理论模拟预测,电场聚焦在微型比色皿内部及上方,且不会积累破坏铜膜的电荷。随后,使用改良的托伦反应方案,在微型比色皿的壁和底部涂上银纳米颗粒。银纳米颗粒充当生物测定介质与构建生物测定的银表面之间产生热梯度的介质。在低功率微波加热下,微型比色皿中的生物测定介质被聚焦电场快速均匀地加热。此外,热梯度的产生导致蛋白质在银纳米颗粒表面快速组装,而不会使蛋白质变性。该ELISA新方法的原理验证通过检测模型蛋白(生物素化牛血清白蛋白,b-BSA)得以证明。在这方面,分别在室温下和微波加热条件下,在市售的96孔高通量筛选(HTS)板和沉积有银纳米颗粒的SRR结构上对浓度范围为(1μM至1 pM)的b-BSA进行检测。虽然室温生物测定(无微波加热)需要70分钟才能完成,但使用SRR结构(有微波加热)进行相同的生物测定只需<2分钟即可完成。使用SRR结构观察到b-BSA的检测下限为0.其比室温ELISA低100倍。