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February 21, 2026Applied Sciences8 citationsOpen Access

Nanomaterials-Enabled Electrochemical Biosensors: From Enhanced Performance to Regulatory Readiness

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VRVirginia RondininiSGStefano GiordaniLDLuisa Stella Dolci

Key Points

  • The aim is to evaluate nanomaterial impact on the performance of electrochemical biosensors and identify regulatory challenges for commercialization.
  • Reviewed nanomaterial classes used in biosensors including carbon nanostructures, gold nanoparticles, and iron-based magnetic nanoparticles.
  • Analyzed how material properties influence biosensor performance metrics like sensitivity and detection limits.
  • Examined the regulatory landscape surrounding the deployment of these technologies in Europe.
  • Identified critical performance factors influenced by nanomaterial characteristics such as morphology and surface chemistry.
  • Highlighted significant barriers to commercialization, including standardization and long-term safety concerns.
  • Outlined relevant European regulations impacting biosensor development and deployment.

Abstract

Electrochemical biosensors represent mature platforms for point-of-need analysis due to their high sensitivity, intrinsic selectivity, low cost, and facile miniaturization. In the last decade, nanomaterials have become integral to advanced biosensor architectures, acting as high-surface-area supports, electron-transfer mediators, and signal-amplifying elements. This review critically examines the most represented nanomaterial classes in mature electrochemical biosensors—carbon nanostructures, gold nanoparticles, and iron-based magnetic nanoparticles—highlighting how morphology, electronic structure, and surface chemistry influence key performance metrics such as limit of detection, linear range, and assay time. Despite a strong technology push and numerous proof-of-concept demonstrations, the translation of nanomaterial-enabled electrochemical biosensors into commercial devices remains limited. This gap arises from the intrinsic physicochemical complexity of nanomaterials, which hampers standardization, reproducibility, and long-term safety assessment. Accordingly, this review integrates performance analysis with a systematic overview of the European regulatory framework, including the Medical Device Regulation (MDR) (EU) 2017/745, the In Vitro Diagnostic Regulation (IVR) (EU) 2017/746, EFSA guidance for food and water applications, and relevant ISO standards, outlining key translational bottlenecks and design principles for deployable biosensing technologies.

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Cite This Study

Rondinini et al. (2026) studied this question.

synapsesocial.com/papers/69994c38873532290d02089fhttps://doi.org/10.3390/app16042048
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