期刊
ACS APPLIED NANO MATERIALS
卷 4, 期 3, 页码 2855-2865出版社
AMER CHEMICAL SOC
DOI: 10.1021/acsanm.0c03483
关键词
ultrathick-shell QDs; core/shell QDs; QD-based fluorescence-linked assay (QDs-FLISA); C-reactive protein; quantitative immunoassay
资金
- National Natural Science Foundation of China [61922028, 61874039, 21671058, 81902158, 21905074]
This study presents a synthesis method for ultra-thick shell quantum dots and their application in C-reactive protein detection, achieving nearly a 3-fold enhancement in detection sensitivity and a 2-fold increase in shelf life. The performance improvements in protein detection are attributed to the use of core/shell quantum dots with high particle stability, high PL QYs, and a large surface area conducive to surface antibody coupling.
Colloidal quantum dots (QDs) have been broadly applied as fluorescent labeling materials in the fields of bio-imaging, sensing, and detection, in which the optical performances and stability of the utilized QDs are vital. Despite significant efforts in developing such materials, it is still challenging to fabricate QDs with high photoluminescence quantum yields (PL QYs) while concurrently possessing high particle and optical stabilities, limiting the further development of QD-based biological labeling and detection techniques. Herein, we report a synthesis of giant CdSe/ZnS/CdZnS/ZnS core/shell QDs with an ultrathick shell (similar to 36 monolayers) and high PL QYs (>80%). We further employ the as-synthesized QDs for C-reactive protein detection, which reach nearly a 3-fold enhancement in detection sensitivity (similar to 0.41 ng/mL) and a 2-fold increase in shelf life, in comparison to the traditional thick-shell QDs (i.e., CdSe/CdS/ZnS core/shell QDs) or commercially available core/shell QDs. We postulate that the performance improvements in protein detection are due to the use of the developed core/shell QDs with high particle stability and PL QYs and large surface area (facilitating surface antibody coupling). Our study demonstrates the viability of applying high-quality core/shell QDs for protein detection with high sensitivity and accuracy.
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