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Calcium-Binding Polymer-Coated Poly(lactide-co-glycolide) Microparticles for Sustained Release of Quorum Sensing Inhibitors to Prevent Biofilm Formation on Hydroxyapatite Surfaces

Authors
Kang, MinjiKim, SungwhanKim, HeejinSong, YoungjunJung, DongwookKang, SunahSeo, Ji-HunNam, SoheeLee, Yan
Issue Date
27-2월-2019
Publisher
AMER CHEMICAL SOC
Keywords
biofilm formation; calcium binding polymer; quorum sensing inhibitors; sustained drug delivery; PLGA microparticles
Citation
ACS APPLIED MATERIALS & INTERFACES, v.11, no.8, pp.7686 - 7694
Indexed
SCIE
SCOPUS
Journal Title
ACS APPLIED MATERIALS & INTERFACES
Volume
11
Number
8
Start Page
7686
End Page
7694
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/67275
DOI
10.1021/acsami.8b18301
ISSN
1944-8244
Abstract
Quorum sensing (QS) inhibitor-based therapy is an attractive strategy to inhibit bacterial biofilm formation without excessive induction of antibiotic resistance. Thus, we designed Ca2+-binding poly(lactide-co-glycolide) (PLGA) microparticles that can maintain a sufficient concentration of QS inhibitors around hydroxyapatite (HA) surfaces in order to prevent biofilm formation on HA-based dental or bone tissues or implants and, therefore, subsequent pathogenesis. Poly(butyl methacrylate-co-methacryloyloxyethyl phosphate) (PBMP) contains both Ca2+-binding phosphomonoester groups and PLGA-interacting butyl groups. The PBMP-coated PLGA (PLGA/PBMP) microparticles exhibited superior adhesion to HA surfaces without altering the sustained release properties of uncoated PLGA microparticles. PLGA/PBMP microparticle-encapsulating furanone C-30, a representative QS inhibitor, effectively inhibited the growth of Streptococcus mutans and its ability to form biofilms on HA surface for prolonged periods of up to 100 h, which was much longer than either furanone C-30 in its free form or when encapsulated in noncoated PLGA microparticles.
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