Department of Bionano Engineering, Center for Bionano Intelligence Education and Research, Hanyang University, Ansan, 426-791, South Korea.
Mikrochim Acta. 2021 Mar 9;188(4):119. doi: 10.1007/s00604-021-04775-4.
The in situ synthesis is reported of citric acid-functionalized ultra-fine bimetallic PtRu alloy nanoparticles (CA@PtRu ANPs) through a simple one-pot wet chemical method. The cost-efficient CA@PtRu ANPs with an average diameter of 3.2 nm revealed to have enhanced surface area, peroxidase-like activity, high stability, and adequate availability of functional groups to bind biomolecules. Along with nanoparticle surface area, the surface charge has also significantly affected the peroxidase-like activity and the colloidal suspension stability. As an excellent immobilization matrix and peroxidase mimic, the CA@PtRu ANPs were utilized to develop non-enzymatic colorimetric immunoassay for rapid, selective, and sensitive quantification of C-reactive protein (CRP) biomarkers. In this immunoassay, CA@PtRu ANPs serve as enzyme mimic that significantly amplifies the color signals, and amine-functionalized silica-coated magnetic microbeads (APTES/SiO@FeO) act as CRP-recognizing capture probes. The absorbance curves of colorimetric immunoassay were measured in wavelengths between 550 and 750 nm, and the maximum absorbance at 652 nm was used to establish a linear relationship between absorbance and CRP concentrations. The developed colorimetric immunoassay showed rapid and sensitive quantification of CRP levels from 0.01 to 180 μg mL with a LOD of 0.01 μg mL. Moreover, the mean recovery of CRP from spiked human serum samples lies between 97 and 109% (n = 3), which indicates that the proposed nanozyme-linked immunoassay has the potential to be used in rapid point-of-care applications.
通过简单的一锅湿化学方法,报道了柠檬酸功能化的超精细双金属 PtRu 合金纳米粒子(CA@PtRu ANPs)的原位合成。具有成本效益的 CA@PtRu ANPs 的平均直径为 3.2nm,具有增强的表面积、过氧化物酶样活性、高稳定性和足够的功能基团可用性,可用于结合生物分子。除了纳米颗粒表面积外,表面电荷也显著影响过氧化物酶样活性和胶体悬浮液稳定性。作为一种优秀的固定化基质和过氧化物酶模拟物,CA@PtRu ANPs 被用于开发非酶比色免疫分析,用于快速、选择性和灵敏地定量 C 反应蛋白(CRP)生物标志物。在这种免疫分析中,CA@PtRu ANPs 用作酶模拟物,可显著放大颜色信号,而胺功能化的硅涂层磁性微球(APTES/SiO@FeO)用作 CRP 识别的捕获探针。比色免疫分析的吸收曲线在 550nm 至 750nm 之间进行测量,并且在 652nm 处的最大吸收用于建立吸光度与 CRP 浓度之间的线性关系。所开发的比色免疫分析显示,CRP 水平在 0.01μgmL 至 180μgmL 范围内具有快速和灵敏的定量能力,LOD 为 0.01μgmL。此外,从人血清样本中添加的 CRP 的平均回收率在 97%至 109%之间(n=3),这表明所提出的纳米酶联免疫分析具有用于快速即时护理应用的潜力。