Wearable biomolecular sensing nanotechnologies in chronic disease management
Creators
Abstract
Over the past decade, consumer wearable sensors have become increasingly ubiquitous in health monitoring, enabling the widespread tracking of key biophysical parameters. The transition towards next-generation body-interfaced biomolecular sensing technologies, fuelled by the integration of reagentless sensing strategies with advanced nanomaterials, marks the next substantial leap forward. These innovations enable unobtrusive, multimodal monitoring of both physiological parameters and biochemical disease markers in real time. This Review examines the current generation of body-interfaced biomolecular sensing technologies, with a particular emphasis on materials innovation and nanotechnological advancements, and discusses their pivotal role in chronic disease monitoring. The discussion extends to the challenges and prospects in this rapidly evolving field, highlighting the potential for materials-focused approaches to transform the landscape of chronic disease monitoring and management with body-interfaced bioelectronics. By harnessing the power of materials and nanotechnological innovations, these biomolecular sensing technologies promise to enhance diagnostic capabilities and foster a more proactive, personalized approach to combating these diseases.
Acknowledgement
This project was supported by the National Science Foundation (grants 2145802 and 2444815), National Institutes of Health (grants R01HL155815, R01HL165002 and R21DK13266), Army Research Office (grant W911NF-23-1-0041), American Cancer Society Research Scholar (grant RSG-21-181-01-CTPS), US Army Medical Research Acquisition Activity (grant HT9425-24-1-0249), Advanced Research Projects Agency for Health Sprint for Women’s Health (award number ARPA-H-ICHUB-24-101-504), Heritage Medical Research Institute, Natural Sciences and Engineering Research Council of Canada and Chan Zuckerberg Biohub Chicago.
Copyright and License
© Springer Nature Limited 2025
Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.
Contributions
These authors contributed equally: Jiaobing Tu, Connor D. Flynn.
Conflict of Interest
The authors declare no competing interests.
Additional details
Identifiers
- PMID
- 41094264
Funding
- National Institutes of Health
- R01HL155815
- National Institutes of Health
- R01HL165002
- National Institutes of Health
- R21DK13266
- National Science Foundation
- 2145802
- National Science Foundation
- 2444815
- United States Army Research Office
- W911NF-23-1-0041
- American Cancer Society
- RSG-21-181-01-CTPS)
- United States Army Medical Research and Development Command
- US Army Medical Research Acquisition Activity HT9425-24-1-0249
- National Institutes of Health
- Sprint for Women’s Health ARPA-H-ICHUB-24-101-504
- Natural Sciences and Engineering Research Council
- Chan Zuckerberg Biohub Chicago
Dates
- Accepted
-
2025-08-06Accepted
- Available
-
2025-10-15Published online