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MMP-8-Responsive Polyethylene Glycol Hydrogel for Intraoral Drug Delivery

  • J. Guo
    ,
  • H. Sun
    ,
  • W. Lei
    ,
  • Y. Tang
    ,
  • S. Hong
    ,
  • H. Yang
*Corresponding author for this work
  • Wuhan University
    ,
  • Xi'an Jiaotong University
    ,
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Abstract

Currently available drug delivery systems for oral diseases suffer from short retention time and poor local concentrations at the target site. A biodegradable stimulus-responsive hydrogel was synthesized in the present study to evaluate its application as an environmentally sensitive carrier for on-demand intraoral drug delivery. The hydrogel was synthesized from diacrylate-containing polyethylene glycol–based scaffolds and a cysteine-terminated peptide crosslinker (CGPQG↓IWGQC) via a Michael-type addition reaction. Because CGPQG↓IWGQC can be cleaved by matrix metalloproteinase 8 (MMP-8), minocycline hydrochloride, bovine serum albumin, or an antibacterial peptide (KSL) was incorporated into the scaffolds to evaluate the MMP-8-responsive release behavior of the on-demand drug delivery system. Hydrogel characterization and gelation kinetics were examined with gel time, Fourier-transform infrared spectroscopy, scanning electron microscopy, and measurements of rheologic parameters. Degradation behavior and MMP-8-responsive drug release were performed by high-performance liquid chromatography and protein-specific assay. Biocompatibility evaluation indicated that the hydrogels were noncytotoxic. Antibacterial testing demonstrated that the released drugs were able to maintain bioactivity. Taken together, these results suggest that the MMP-8-sensitive hydrogel is a promising candidate for on-demand intraoral localized drug delivery. Because MMP-8 is one of the most important biomarkers for periodontitis, the MMP-8-responsive hydrogel has potential to be used for in situ adaptive degradation in response to chronic periodontitis and peri-implantitis. This notion has to be tested in animal models of periodontal disease.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 564-571 (8 pages)

Journal (Volume, Issue Number)

Journal of Dental Research (Volume 98, Issue 5)

Publication milestones

  • Published - 05/01/2019

Publication status

Published - 05/01/2019

ISSN

0022-0345

Publication IDs

  • Scopus: 85063035994
  • PubMed: 30876379

Publication metrics

Metrics

SciVal
citations
13
Fractional count
1
Fractional count
0.13
Fractional count
7
Fractional count
0.88
Fractional count
1
Fractional count
1
Scopus
citations
SciVal
FWCI
4.17
SciVal
Author count
8
SciVal
Paper percentile
92
SciVal
Top percentile
10

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Citation count
67
Captures
68

Funding Details

The authors thank Professor Xianzheng Zhang, Department of Chemistry, Wuhan University, for providing facilities and materials. This work was financially supported by the National Nature Science Foundation of China (No. 81771112), Hubei Natural Science Foundation (No. 2015CFA072), and the Fundamental Research Funds for the Central Universities (No. 2015304020201). The authors declare no potential conflicts of interest with respect to the authorship and/or publication of this article. The authors thank Professor Xianzheng Zhang, Department of Chemistry, Wuhan University, for providing facilities and materials.