Department of Chemistry, College of Natural Sciences , Seoul National University , Gwanak-ro 1 , Gwanak-gu, Seoul 08826 , Republic of Korea.
Department of Materials Science and Engineering , Korea University , 145 Anam-ro , Seongbuk-gu, Seoul 02841 , Republic of Korea.
ACS Appl Mater Interfaces. 2019 Feb 27;11(8):7686-7694. doi: 10.1021/acsami.8b18301. Epub 2019 Feb 15.
Quorum sensing (QS) inhibitor-based therapy is an attractive strategy to inhibit bacterial biofilm formation without excessive induction of antibiotic resistance. Thus, we designed Ca-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 Ca-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.
群体感应 (QS) 抑制剂为基础的治疗策略是一种有吸引力的方法,可以抑制细菌生物膜的形成,而不会过度诱导抗生素耐药性。因此,我们设计了 Ca 结合的聚(乳酸-共- 乙醇酸)(PLGA)微球,这些微球可以在羟基磷灰石(HA)表面周围保持足够浓度的 QS 抑制剂,以防止 HA 基牙科或骨组织或植入物上的生物膜形成,从而防止随后的发病机制。聚(丁基甲基丙烯酸酯-共-甲基丙烯酰氧基乙基磷酸酯)(PBMP)既含有 Ca 结合的磷酸单酯基团,又含有与 PLGA 相互作用的丁基基团。涂有 PBMP 的 PLGA(PLGA/PBMP)微球表现出对 HA 表面的优异附着力,而不会改变未涂覆的 PLGA 微球的持续释放特性。用呋喃酮 C-30(一种代表性的 QS 抑制剂)封装的 PLGA/PBMP 微球能够有效抑制变形链球菌的生长及其在 HA 表面形成生物膜的能力,长达 100 小时,比游离形式的呋喃酮 C-30 或封装在非涂覆的 PLGA 微球中长得多。