Journal
SENSORS AND ACTUATORS B-CHEMICAL
Volume 366, Issue -, Pages -Publisher
ELSEVIER SCIENCE SA
DOI: 10.1016/j.snb.2022.131947
Keywords
Smart hydrogel aptasensor; Dual-mode detection platform; Visual fluorescence; Microfluidic chip; Pathogens; Gold nanoclusters
Funding
- National Natural Science Foundation of China [21974074]
- Natural Science Foundation of Ningbo [2019A610184, 2019A610142, 2019A610013, 202002N3195]
- Zhejiang Province Natural Science Foundation [LY19B050001, LY20B050004]
- Zhejiang Province Welfare Technology Applied Research Project [LGC22B050011, LGC20B050006]
- Xinmiao Talent Program [2021R428004]
- K. C. Wong Magna Fund in Ningbo University
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In this study, a smart hydrogel aptasensor was developed for the quantitative detection of Vibrio parahaemolyticus in water samples. The aptasensor utilized a dual-mode detection strategy combining visual fluorescence and microfluidic chip methods. The results showed that the aptasensor was able to detect low concentrations of V.P in just 45 minutes. The dual-mode sensing platform offers the advantages of quantitative and on-site detection of live pathogens, as well as shortened detection period.
Usually, a low concentration of pathogens proliferate rapidly in waters to cause serious threats to human health. It is necessary to develop on-site and speedy assays to detect them. In this work, a smart hydrogel aptasensor was assembled in Eppendorf tubes for quantifying Vibrio parahaemolyticus (V.P). It employed a dual-mode detection strategy combining visual fluorescence (FL) and microfluidic chip (MC) methods. In this aptasensor, the hydrogel contained ATP aptamer together with gold nanoclusters (AuNCs) as signal tags, and V.P aptamer was modified on tube lids. Firstly, trace V.P in waters was specifically enriched by the lid and then hydrolyzed to release ATP which was combined with ATP aptamer in hydrogel to form ATP-aptamer complex. The complex together with AuNCs was subsequently released into the supernatant for dual-mode detection. ATP-aptamer was detected by MC and AuNCs by FL. By the assay, as low as 100 CFU.mL(-1) V.P was determined by FL within 45 min and 10 CFU.mL(-1) by MC. The dual-mode sensing platform exhibits the following advantages: Firstly, live pathogens were quantitatively and on-site detected. Secondly, the lid's enrichment of V.P and signal transduction from one V.P to 10(14) ATP could double-amplify signals and increase the detection efficiency. Finally, the samples quickly screened by visual FL on-site, and then accurately quantified by MC in the laboratory, which greatly shortens the detection period. It has been successfully utilized for on-site detecting V.P in aquatic waters and could be extended to other bacteria measurements through changing the relative aptamer on the tube lid.
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