Artificial Intelligence-Aided Massively Parallel Spectroscopy of Freely Diffusing Nanoscale Entities

被引:3
|
作者
Hlavacek, Antonin [1 ]
Uhrova, Katercina [1 ]
Weisova, Julie [1 ]
Krcivankova, Jana [1 ]
机构
[1] Czech Acad Sci, Inst Analyt Chem, Veveri 97, Brno 60200, Czech Republic
关键词
CROSS-CORRELATION SPECTROSCOPY; FLUORESCENCE CORRELATION SPECTROSCOPY; LINKED IMMUNOSORBENT-ASSAY; UP-CONVERSION; NANOPARTICLES; MICROSCOPY;
D O I
10.1021/acs.analchem.3c01043
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Massively parallelspectroscopy (MPS) of many single nanoparticlesin an aqueous dispersion is reported. As a model system, bioconjugatedphoton-upconversion nanoparticles (UCNPs) with a near-infrared excitationare prepared. The UCNPs are doped either with Tm3+ (emission450 and 802 nm) or Er3+ (emission 554 and 660 nm). TheseUCNPs are conjugated to biotinylated bovine serum albumin (Tm3+-doped) or streptavidin (Er3+-doped). MPS is correlatedwith an ensemble spectra measurement, and the limit of detection (1.6fmol L-1) and the linearity range (4.8 fmol L-1 to 40 pmol L-1) for bioconjugatedUCNPs are estimated. MPS is used for observing the bioaffinity clusteringof bioconjugated UCNPs. This observation is correlated with a nativeelectrophoresis and bioaffinity assay on a microtiter plate. A competitiveMPS bioaffinity assay for biotin is developed and characterized witha limit of detection of 6.6 nmol L-1. MPS from complexbiological matrices (cell cultivation medium) is performed withoutincreasing background. The compatibility with polydimethylsiloxanemicrofluidics is proven by recording MPS from a 30 & mu;m deep microfluidicchannel.
引用
收藏
页码:12256 / 12263
页数:8
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