4.7 Article

A turn-on-type fluorescence resonance energy transfer aptasensor for vibrio detection using aptamer-modified polyhedral oligomeric silsesquioxane-perovskite quantum dots/Ti3C2 MXenes composite probes

Journal

MICROCHIMICA ACTA
Volume 188, Issue 2, Pages -

Publisher

SPRINGER WIEN
DOI: 10.1007/s00604-020-04679-9

Keywords

Vibrio parahaemolyticus; Fluorescence resonance energy transfer; Polyhedral oligomeric silsesquioxane-perovskite; Quantum dots; Ti3C2 MXenes; Turn-on-type aptasensor

Funding

  1. National Natural Science Foundation of China [21974074]
  2. Natural Science Foundation of Ningbo [2019A610013, 2019A610142, 2019A610184, 2019A610197, 2018A610182, 2018A610221]
  3. Zhejiang Province Welfare Technology Applied Research Project [LY19B050001, LY18B070004]
  4. Zhejiang Province Public Welfare Technology Application Research Analysis Test Plan [LGC19B070003, LGC20B050006]
  5. Guangdong Provincial Key Laboratory of Environmental Pollution and Health [GDKLEEH201807]
  6. K. C. Wong Magna Fund in Ningbo University

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A novel aptasensor based on POSS-PQDs-Apt and Ti3C2 MXenes composite probes was prepared and successfully applied for VP detection relying on FRET. The method can rapidly and accurately detect VP in the concentration range of 10(2) - 10(6) cfu/mL, suitable for online monitoring in aquaculture industry. The detection method showed good feasibility in screening VP through testing actual seawater samples.
A pair of composite probes based on aptamer modified polyhedral oligomeric silsesquioxane-perovskite quantum dots (POSS-PQDs-Apt) as signal probe and titanium carbide (Ti3C2) MXenes as quencher were prepared for the first time. They were employed to fabricate one turn-on-type aptasensor relying on fluorescence resonance energy transfer (FRET) for Vibrio parahaemolyticus (VP) determination. The POSS-PQDs-Apt can be adsorbed on the MXenes nanosheets, and its fluorescence was quenched due to the FRET. After the composite probes were incubated with VP for 50 min, the POSS-PQDs-Apt binding with VP can be released from the surface of MXenes, and the signal recovered due to its higher affinity to the VP than MXenes. The fluorescence intensity from 519 nm emission of the system was measured at 480 nm excitation. Under In optimized conditions, the assay can determine VP in the concentration range 10(2) - 10(6) cfu/mL, and the detection limit (LOD) was 30 cfu/mL using fluorescence detection. The LOD is still 100 cfu/mL by naked eye detection which is proper for on-line monitoring VP in aquaculture water. This method was also used to detect VP in actual samples of seawater, the recovery of spiked samples was between 93% and 106%, and relative standard deviation (RSD) was between 2.7% and 6.7%. The result is consistent with the plate count. Therefore, this assay could provide a candidate platform for screening VP in aquaculture industry.

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