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Nanozyme-Enhanced Paper-Based Bipolar Electrode Biosensor for Dual-Mode Detection for M918T in Serum with Single-Base
Chen-Fang Miao1, Yu Zhang1, Zhen Lin1
1Department of Pharmaceutical Analysis, Higher Educational Key Laboratory for Nano Biomedical Technology of Fujian Province, School of Pharmacy, Fujian Medical University, Fuzhou 350122, China.
A novel dual-mode biosensor detects the ultralow RET M918T mutation, a key biomarker for medullary thyroid carcinoma (MTC). This paper-based system offers sensitive, single-base resolution for early MTC screening and point-of-care testing.
Area of Science:
- Biomedical Engineering
- Analytical Chemistry
- Molecular Diagnostics
Background:
- The RET M918T mutation is a crucial biomarker for early medullary thyroid carcinoma (MTC) screening.
- Ultralow abundance of M918T mutations poses detection challenges for conventional methods, limiting point-of-care testing (POCT).
Purpose of the Study:
- To develop a sensitive, single-base resolution detection method for the RET M918T mutation.
- To create a dual-modal biosensor for reliable MTC screening and POCT.
Main Methods:
- Designed a paper-based bipolar electrode-electrochemiluminescence (BPE-ECL) and colorimetry dual-modal biosensor.
- Integrated 2'-fluorinated nucleotide (2'-FN) Y-shaped junctions for enhanced mismatch discrimination.
- Utilized g-C3N4@FeMOFs nanozyme for dual amplification of ECL and colorimetric signals.
Main Results:
- Achieved limits of detection of 0.76 pM (ECL) and 1.4 pM (colorimetry) for M918T.
- Demonstrated successful application in human serum samples.
- Validated results through mutual self-validation of dual signals, avoiding false positives.
Conclusions:
- The developed dual-mode biosensor provides a rapid, low-cost, and portable platform for MTC biomarker detection.
- This strategy shows significant potential for early diagnosis and on-site screening of MTC.
- The biosensor enables sensitive and reliable detection of ultralow abundance mutations.
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