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Large-area grown ultrathin molybdenum oxides for label-free sensitive biomarker detection
The rise of two-dimensional (2D) materials has provided a confined geometry and yielded methods for guiding electrons at the nanoscale level. 2D material-enabled electronic devices can interact and transduce the subtle charge perturbation and permit significant advancement in molecule discrimination...
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Published in: | Nanoscale 2024-07, Vol.16 (27), p.1361-137 |
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Main Authors: | , , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
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Summary: | The rise of two-dimensional (2D) materials has provided a confined geometry and yielded methods for guiding electrons at the nanoscale level. 2D material-enabled electronic devices can interact and transduce the subtle charge perturbation and permit significant advancement in molecule discrimination technology with high accuracy, sensitivity, and specificity, leaving a significant impact on disease diagnosis and health monitoring. However, high-performance biosensors with scalable fabrication ability and simple protocols have yet to be fully realized due to the challenges in wafer-scale 2D film synthesis and integration with electronics. Here, we propose a molybdenum oxide (MoO
x
)-interdigitated electrode (IDE)-based label-free biosensing chip, which stands out for its wafer-scale dimension, tunability, ease of integration and compatibility with the complementary metal-oxide-semiconductor (CMOS) fabrication. The device surface is biofunctionalized with monoclonal anti-carcinoembryonic antigen antibodies (anti-CEA)
via
the linkage agent (3-aminopropyl)triethoxysilane (APTES) for carcinoembryonic antigen (CEA) detection and is characterized step-by-step to reveal the working mechanism. A wide range and real-time response of the CEA concentration from 0.1 to 100 ng mL
−1
and a low limit of detection (LOD) of 0.015 ng mL
−1
were achieved, meeting the clinical requirements for cancer diagnosis and prognosis in serum. The MoO
x
-IDE biosensor also demonstrates strong surface affinity towards molecules and high selectivity using
l
-cysteine (
l
-Cys), glycine (Gly), glucose (Glu), bovine serum albumin (BSA), and immunoglobulin G (IgG). This study showcases a simple, scalable, and low-cost strategy to create a nanoelectronic biosensing platform to achieve high-performance cancer biomarker discrimination capabilities.
A molybdenum oxide (MoO
x
)-interdigitated electrode (IDE)-based label-free biosensing chip, functionalized with anti-carcinoembryonic antigen antibodies
via
APTES, achieves a wide range and low limit of detection for CEA. |
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ISSN: | 2040-3364 2040-3372 2040-3372 |
DOI: | 10.1039/d4nr01275e |