1. Introduction
Breast cancer remains one of the most significant causes of morbidity and mortality among women globally. Traditional diagnostic approaches, such as tissue biopsies, though effective, are often invasive, expensive, and require considerable clinical expertise. This study addresses the growing need for less invasive, rapid, and cost-effective diagnostic alternatives by exploring a liquid biopsy-based strategy using microRNA detection. Specifically, it introduces a novel electrochemical biosensor designed to identify miRNA-34a, a known biomarker of breast cancer, thereby offering a promising solution for early and accurate disease detection.
2. Development of a Two-Dimensional Nanocomposite-Based Biosensor
The biosensor developed in this research employs a composite of reduced graphene oxide (rGO) and molybdenum disulfide (MoS₂), chosen for their synergistic physicochemical properties. These two-dimensional materials exhibit high surface area and electrical conductivity, which are crucial for improving biosensor sensitivity. Furthermore, the sulfur atoms in MoS₂ facilitate the anchoring of metallic nanoparticles, such as gold, enhancing probe immobilization. This strategic combination forms the basis of a powerful sensing platform suitable for the electrochemical detection of nucleic acid biomarkers.
3. Functionalization and Enhancement via Gold Nanoparticles
Gold nanoparticles (AuNPs) play a pivotal role in the biosensor’s performance by enhancing conductivity and enabling robust probe immobilization through thiol-gold covalent bonds. The incorporation of AuNPs onto the surface of the SPrGO/MoS₂ composite electrode not only increases the electrochemical activity but also provides high affinity for thiolated DNA probes. This ensures specific and stable hybridization with the target miRNA-34a, enabling precise detection with minimal background interference.
4. Electrochemical Detection Mechanism
The detection strategy utilizes differential pulse voltammetry (DPV), a highly sensitive electrochemical technique, to monitor hybridization events. The current signal generated by the redox activity of ferrocyanide reflects the presence and concentration of miRNA-34a. The biosensor demonstrates a wide linear detection range from 0.1 nM to 1000 nM and an impressively low detection limit of 66 pM. This sensitivity is crucial for detecting miRNA-34a in clinical samples, where biomarker concentrations are often very low.
5. Clinical Applicability and Performance Validation
The biosensor was evaluated using serum samples spiked with varying concentrations of miRNA-34a, representing low, medium, and high levels typically seen in patient populations. The results demonstrated high precision, accuracy, and repeatability, highlighting the potential of this platform for clinical diagnostics. The sensor’s stability and ease of use further support its application in point-of-care settings, especially in resource-limited environments where traditional biopsy procedures may not be feasible.
6. Future Perspectives and Applications
The development of this SPrGO/MoS₂-based biosensor marks a significant step forward in the field of electrochemical diagnostics. Its capability to accurately detect miRNA-34a offers a foundation for expanding the platform to other miRNA biomarkers associated with various cancers or diseases. With further validation, such biosensors could become standard tools for early cancer detection, treatment monitoring, and potentially for personalized medicine approaches, bridging the gap between laboratory research and real-world clinical application.
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