788 Petit Science Center, Department of Chemistry, Center for Diagnostics and Therapeutics, Georgia State University, Atlanta, GA 30302, USA.
790 Petit Science Center, Institute of Biomedical Science, Georgia State University and Atlanta Veterans Affairs Medical Center, Atlanta, GA 30033, USA.
Analyst. 2023 May 2;148(9):2064-2072. doi: 10.1039/d3an00252g.
We designed a simple, inexpensive, and user-friendly assay using mesoporous silica nanoparticles to detect analytes. Highly stable and uniform palladium nanoparticles covered with mesoporous silica (Pd@mSiO) were generated and characterized extensively using physical methods. Human Serum Albumin (HSA) protein or ssDNA specific to the HIV gag region was capped onto the Pd@mSiO electrostatically. This "cap" prevented the Pd(0) inside the mesoporous silica nanoparticles from catalyzing the conversion of non-fluorescent molecules to fluorescent molecules. In the presence of target anti-HSA antibodies or complementary sequence (HIV gag), HSA protein or DNA cap dissociated from the surface of Pd@mSiO-NH through the specific antigen-antibody reaction or DNA hybridization, allowing Pd(0) to convert the non-fluorescent molecules to fluorescent molecules. The limit and range of detection of anti-HSA antibodies were 3.8 nM and 3.8 nM to 133.3 nM, respectively. The limit and range of detection of HIV gag were 1.6 nM and 1.6 nM to 15 nM, respectively. This simple, inexpensive, "add sample and measure" diagnostic assay could potentially be incorporated into point of care diagnostics for low-resource settings.
我们设计了一种简单、廉价且用户友好的分析方法,使用介孔硅纳米粒子来检测分析物。高度稳定且均匀的钯纳米粒子覆盖有介孔硅(Pd@mSiO),并通过物理方法进行了广泛的生成和表征。人血清白蛋白(HSA)蛋白或针对 HIV gag 区域的 ssDNA 特异性地通过静电作用固定在 Pd@mSiO 上。这种“盖子”阻止了介孔硅纳米粒子内部的 Pd(0)催化非荧光分子转化为荧光分子。在存在靶抗-HSA 抗体或互补序列(HIV gag)的情况下,HSA 蛋白或 DNA 帽通过特异性抗原-抗体反应或 DNA 杂交从 Pd@mSiO-NH 的表面解离,从而允许 Pd(0)将非荧光分子转化为荧光分子。抗-HSA 抗体的检测限和检测范围分别为 3.8 nM 和 3.8 nM 至 133.3 nM。HIV gag 的检测限和检测范围分别为 1.6 nM 和 1.6 nM 至 15 nM。这种简单、廉价、“添加样品并测量”的诊断分析方法有可能被纳入资源匮乏环境下的即时诊断。