4.6 Article

Cell Membrane and V2C MXene-Based Electrochemical Immunosensor with Enhanced Antifouling Capability for Detection of CD44

期刊

ACS SENSORS
卷 7, 期 9, 页码 2701-2709

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acssensors.2c01215

关键词

electrochemical immunosensor; cell membrane; V2C MXene; antifouling; CD44

资金

  1. National Natural Science Foundation of China [22004130, 21973111]
  2. Fundamental Research Funds for the Central Universities [3122021056]
  3. Scientific Research Project of Tianjin Education Commission [2021KJ057]

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The study presents a simple and sensitive sandwich-type antifouling immunoassay, utilizing native cell membranes to endow electrochemical surfaces with antifouling and biocompatible features. The biosensor combines platelet membrane/Au nanoparticle/delaminated V2C nanosheet modified electrode as the substrate of sensing interface and methylene blue/aminated metal organic framework as an electrochemical signal probe. The developed biosensor demonstrates excellent antifouling properties, enabling ultrasensitive detection of CD44 and CD44-positive cancer cells in complex liquids.
The inactive adsorption and interference of biomolecules in electrochemical biosensors is a topic of intense interest. Directly utilizing native cell membranes to endow electrochemical surfaces with antifouling and biocompatible features is a promising strategy, rather than attempting to synthetically replicate complex biological interface properties. In this study, we present a facial and sensitive sandwich-type antifouling immunoassay through platelet membrane/Au nanoparticle/delaminated V2C nanosheet (PM/AuNPs/d-V2C)-modified electrode as the substrate of sensing interface and methylene blue/aminated metal organic framework (MB@NH2-Fe-MOF-Zn) as an electrochemical signal probe. The biosensor perfectly integrates the high conductivity of AuNPs-loaded V2C MXene with the excellent loading property of NH2-Fe-MOF-Zn to improve the electrochemical sensing performance. In addition, the excellent antifouling properties of the homogeneous cell membrane can effectively prevent the non-specific adsorption of model proteins. The obtained antifouling biosensor possesses the capability of ultrasensitive detection of CD44 and CD44-positive cancer cell in complex liquids and exhibits good analytical performance for the analysis of CD44 with a linear range from 0.5 ng/mL to 500 ng/mL. This strategy of developing cell membrane-based biosensing systems with enhanced antifouling capability can be easily expanded to the construction of other complex biosensors, and the advanced biological probes and analytical methods provide a favorable means to accurately quantify biomarkers associated with tumor progression.

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