4.4 Review

Recent Advances of using Personal Glucose Meter as a Biosensor Readout for Non-glucose Targets

期刊

CURRENT ANALYTICAL CHEMISTRY
卷 18, 期 6, 页码 705-722

出版社

BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/1573411017666210804105750

关键词

Personal glucose meter; non-glucose target; point of care; biosensor; signal transduction; signal amplification; target recognition

资金

  1. Research Foundation of Education Bureau of Hunan Province [19B384]
  2. Open Project of State Key Laboratory of Chemo/biosensing and Chemometrics [2016010]
  3. China Postdoctoral Science Foundation [2015M5 82339]
  4. Changde Science and Technology Innovation Project [2019ZD25, 2020ZD29]
  5. US National Institute of Health [GM141931, MH110975]

向作者/读者索取更多资源

This review summarizes the recent advances of PGM-based biosensors for non-glucose targets, including signal transduction, signal amplification, and target molecule recognition and analysis. Current challenges and future directions are also discussed.
Background: Personal Glucose Meter (PGM) has become the most successful biosensor in past decades due to its advantages of small size, convenient operation, and low cost. To take advantage of many years of research and development of PGMs, new signal transduction methods have been developed to expand the PGM from simple monitoring of blood glucose to the detection of numerous non-glucose targets. Objectives: This review summarizes recent advances of PGM-based biosensors for non-glucose targets, including signal transduction, signal amplification, and target molecule recognition and analysis. Current challenges and future directions are also discussed. Conclusion: PGM can be used as a biosensor readout to detect various non-glucose targets from metal ion, small molecules to protein and even living organisms such as bacteria and other pathogens by using different signal transduction elements such as invertase and amylase, and different signal amplification methods such as nanomaterials, nucleic acid reaction, liposome encapsulation, hydrogel trapping, DNAzyme amplification and biotin-streptavidin reaction.

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