Integrating enzyme-nanoparticles bring new prospects for the diagnosis and treatment of immune dysregulation in periodontitis

Front Cell Infect Microbiol. 2024 Nov 1:14:1494651. doi: 10.3389/fcimb.2024.1494651. eCollection 2024.

Abstract

Enzymes play a significant role in mediating inflammatory and immune responses in periodontitis. Effective diagnosis, timely treatment, and continuous management of periodontal enzymes are essential to prevent undesirable consequences; however, this remains a significant challenge. Nanoparticles (NPs) have attracted significant attention in biomedicine because of their advantageous nanosized effects. NPs are conjugated with specific enzyme substrates at responsive sites that are triggered by periodontitis enzyme biomarkers, leading to functional or characteristic changes. In contrast, NPs with enzyme-mimetic activities exhibit catalytic activity, effectively destroying pathogenic biofilms and modulating the immune response in periodontitis. The unique properties of enzyme-targeting NPs have enabled the development of biosensors and fluorescent probes capable of identifying enzyme biomarkers associated with periodontitis. Enzyme-responsive and enzyme-mimetic NPs both exert therapeutic applications in the treatment of periodontitis. In this review, we provide a comprehensive overview of the enzymes associated with periodontitis, the mechanisms of enzyme-responsive and enzyme-mimetic NPs, recent advancements in the use of NPs for detecting these enzymes, and the therapeutic applications of NPs in targeting or mimicking enzyme functions. We also discuss the challenges and prospects of using NPs in the diagnosis and treatment of periodontitis.

Keywords: biosensors; enzyme-responsive nanoparticles; fluorescent probes; inflammatory; nanozymes; periodontitis biomarkers.

Publication types

  • Review

MeSH terms

  • Animals
  • Biofilms / drug effects
  • Biomarkers
  • Biosensing Techniques / methods
  • Enzymes / metabolism
  • Humans
  • Nanoparticles* / chemistry
  • Periodontitis* / diagnosis
  • Periodontitis* / drug therapy
  • Periodontitis* / immunology

Substances

  • Enzymes
  • Biomarkers

Grants and funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. The authors were supported by Medical Research Foundation of Guangdong Province A2024608 (QZ); Guangdong Basic and Applied Basic Research Foundation 2023A1515011945 (QZ, YD, and LM); Municipal Financial Subsidy of Shenzhen Medical Key Discipline Construction (QZ, JC, YD, HM, and LM).