4.6 Article

An Electrochemical Ti3C2Tx Aptasensor for Sensitive and Label-Free Detection of Marine Biological Toxins

期刊

SENSORS
卷 21, 期 14, 页码 -

出版社

MDPI
DOI: 10.3390/s21144938

关键词

Ti3C2Tx; aptamer; saxitoxin; marine toxins; electrolyte-insulator semiconductor

资金

  1. National Natural Science Foundation of China [51861145307, 32071370, 31700859]
  2. Postdoctoral Research Foundation of China [2018M633524, 2017M613127]
  3. Fundamental Research Funds for the Central Universities [xjj2017136]

向作者/读者索取更多资源

An EIS sensor based on MXene nanosheets was developed for STX detection, achieving high sensitivity and good specificity through aptamer modification, with a low detection limit of 0.03 nM. The method demonstrated good selectivity and stability, showing potential for detecting STX in real samples.
Saxitoxin (STX) belongs to the family of marine biological toxins, which are major contaminants in seafood. The reference methods for STX detection are mouse bioassay and chromatographic analysis, which are time-consuming, high costs, and requirement of sophisticated operation. Therefore, the development of alternative methods for STX analysis is urgent. Electrochemical analysis is a fast, low-cost, and sensitive method for biomolecules analysis. Thus, in this study, an electrolyte-insulator-semiconductor (EIS) sensor based on aptamer-modified two-dimensional layered Ti3C2Tx nanosheets was developed for STX detection. The high surface area and rich functional groups of MXene benefited the modification of aptamer, which had specific interactions with STX. Capacitance-voltage (C-V) and constant-capacitance (ConCap) measurement results indicated that the aptasensor was able to detect STX with high sensitivity and good specificity. The detection range was 1.0 nM to 200 nM and detection limit was as low as 0.03 nM. Moreover, the aptasensor was found to have a good selectivity and two-week stability. The mussel tissue extraction test suggested the potential application of this biosensor in detecting STX in real samples. This method provides a convenient approach for low-cost, rapid, and label-free detection of marine biological toxins.

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