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Biofunctionalized two-dimensional Ti3C2 MXenes for ultrasensitive detection of cancer biomarker

In this work, ultrathin Ti3C2-MXene nanosheets were synthesized by minimally intensive layer delamination methods, and uniformly functionalized with aminosilane (f-Ti3C2-MXene) to provide a covalent binding for the immobilized bio-receptor (anti-CEA) for label free, ultrasensitive detection of cance...

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Published in:Biosensors & bioelectronics 2018-12, Vol.121, p.243-249
Main Authors: Kumar, Saurabh, Lei, Yongjiu, Alshareef, Niman H., Quevedo-Lopez, M.A., Salama, Khaled N.
Format: Article
Language:English
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Summary:In this work, ultrathin Ti3C2-MXene nanosheets were synthesized by minimally intensive layer delamination methods, and uniformly functionalized with aminosilane (f-Ti3C2-MXene) to provide a covalent binding for the immobilized bio-receptor (anti-CEA) for label free, ultrasensitive detection of cancer biomarker (carcinoembryonic antigen, CEA). The effect of different redox probes on the electrochemical behavior of f-Ti3C2-MXene was investigated and found that hexaammineruthenium ([Ru(NH3)6]3+) is the preferable redox probe for biosensing. The fabricated biofunctionalized Ti3C2-MXene exhibits a linear detection range of 0.0001–2000 ng mL−1 with sensitivity of 37.9 µA ng−1 mL cm−2 per decade. The wider linear detection range of our f-Ti3C2-MXene is not only higher than previously reported pristine 2D nanomaterials, but is even comparable to other hybrid 2D nanomaterials. We believe that this work opens a new window for development of MXene-based highly sensitive DNA, aptamer, enzyme, antibody, and cell based biosensors, and could be further used in drug delivery application. •Two-dimensional Ti3C2-MXene nanosheets were synthesized by the MILD method.•Single/few layered MXene nanosheets were functionalized via APTES (f-Ti3C2-MXene).•The electrochemical behavior of f-Ti3C2-MXene was explored.•f-Ti3C2-MXene was biofunctionalized for electrochemical detection of CEA.•It exhibits a wide linear detection range of 0.0001–2000 ng mL−1.
ISSN:0956-5663
1873-4235
DOI:10.1016/j.bios.2018.08.076