Jia Tianwei, Saikam Varma, Luo Ying, Sheng Xiaolin, Fang Jieqiong, Kumar Mukesh, Iyer Suri S
788 Petit Science Center, Department of Chemistry, Center for Diagnostics and Therapeutics, Georgia State University, Atlanta, Georgia 30302, United States.
622 Petit Science Center, Department of Biology, Georgia State University, Atlanta, Georgia 30302, United States.
ACS Omega. 2024 Mar 12;9(12):14604-14612. doi: 10.1021/acsomega.3c06136. eCollection 2024 Mar 26.
Early detection and viral concentration monitoring of human immunodeficiency virus in resource-poor settings are important to control disease spread and reduce mortality. Nucleic acid amplification tests are expensive for low-resource settings. Lateral flow antibody tests are not sensitive if testing is performed within 7-10 days, and these tests are not quantitative. We describe a signal enhancement technique based on fluorescent silica nanoparticles and bioorthogonal chemistries for the femtomolar detection of the HIV-1 p24 antigen. We developed a magnetic bead-based assay, wherein we used fluorescent-dye-encapsulated silica nanoparticles as reporters. The number of reporters was increased by using bioorthogonal chemistry to provide signal enhancement. The limit and range of detection of the sandwich immunoassay using alternating multiple layers for p24 in human serum were found to be 46 fg/mL (1.84 fM) and 46 fg/mL to 10 ng/mL, respectively. This simple assay was 217-fold higher in sensitivity compared to that of commercial enzyme-linked immunoassays (limit of detection of 10 pg/mL).
在资源匮乏地区对人类免疫缺陷病毒进行早期检测和病毒浓度监测对于控制疾病传播和降低死亡率至关重要。核酸扩增检测对于资源有限的地区来说成本高昂。如果在7至10天内进行检测,侧向流动抗体检测并不灵敏,而且这些检测无法进行定量。我们描述了一种基于荧光二氧化硅纳米颗粒和生物正交化学的信号增强技术,用于飞摩尔级检测HIV-1 p24抗原。我们开发了一种基于磁珠的检测方法,其中我们使用包裹荧光染料的二氧化硅纳米颗粒作为报告分子。通过使用生物正交化学增加报告分子的数量以实现信号增强。发现在人血清中使用交替多层夹心免疫测定法检测p24的检测限和检测范围分别为46 fg/mL(1.84 fM)和46 fg/mL至10 ng/mL。这种简单的检测方法与商业酶联免疫测定法(检测限为10 pg/mL)相比,灵敏度高出217倍。