高分子科学(英文版)2024,Vol.42Issue(6) :718-728.DOI:10.1007/s10118-024-3094-8

Triclosan-conjugated,Lipase-responsive Polymeric Micelles for Eradication of Staphylococcal Biofilms

Yan-Qiang Huang Yuan-Feng Li Yong Liu Lin-Qi Shi
高分子科学(英文版)2024,Vol.42Issue(6) :718-728.DOI:10.1007/s10118-024-3094-8

Triclosan-conjugated,Lipase-responsive Polymeric Micelles for Eradication of Staphylococcal Biofilms

Yan-Qiang Huang 1Yuan-Feng Li 2Yong Liu 3Lin-Qi Shi4
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作者信息

  • 1. Guangxi Technology Innovation Cooperation Base of Prevention and Control Pathogenic Microbes with Drug Resistance,Youjiang Medical University for Nationalities,Baise533000,China
  • 2. Translational Medicine Laboratory,the First Affiliated Hospital of Wenzhou Medical University,Wenzhou 325035,China
  • 3. Guangxi Technology Innovation Cooperation Base of Prevention and Control Pathogenic Microbes with Drug Resistance,Youjiang Medical University for Nationalities,Baise533000,China;Wenzhou Institute,University of Chinese Academy of Sciences,Wenzhou 325001,China;State Key Laboratory of Medicinal Chemical Biology,Key Laboratory of Functional Polymer Materials of Ministry of Education,and Institute of Polymer Chemistry,College of Chemistry,Nankai University,Tianjin 300071,China
  • 4. State Key Laboratory of Medicinal Chemical Biology,Key Laboratory of Functional Polymer Materials of Ministry of Education,and Institute of Polymer Chemistry,College of Chemistry,Nankai University,Tianjin 300071,China
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Abstract

Bacterial biofilms present a significant challenge in treating drug-resistant infections,necessitating the development of innovative nanomedicines.In this study,we introduce triclosan-conjugated,lipase-responsive polymeric micelles designed to exploit biofilm properties and serve as a responsive drug delivery platform.The micelles were created using an amphiphilic block polymer synthesized via ring-opening poly-merization of e-caprolactone(CL)and triclosan-containing cyclic trimethylene carbonate(MTC-Tri).Poly(ethylene glycol)(PEG-OH)acted as the macro-initiator,resulting in micelles with a PEG shell that facilitated their penetration into bacterial biofilms.An important advantage of our mi-celles lies in their interaction with local bacterial lipases within biofilms.These lipases triggered rapid micelle degradation,releasing triclosan in a controlled manner.This liberated triclosan effectively eliminated bacteria embedded in the biofilms.Notably,the triclosan-conjugated micelles displayed minimal toxicity to murine fibroblasts,indicating their biocompatibility and safety.This finding emphasizes the potential application of these micelles in combatting drug resistance observed in bacterial biofilms.Our triclosan-conjugated,lipase-responsive polymeric micelles ex-hibit promising characteristics for addressing drug resistance in bacterial biofilms.By harnessing biofilm properties and implementing a respon-sive drug delivery system,we seek to provide an effective solution in the fight against drug-resistant bacteria.

Key words

Self-assembly/Polymer prodrug/Ring-opening polymerization/Biofilm eradication/Cytotoxicity

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基金项目

国家自然科学基金(22275043)

国家自然科学基金(52203184)

国家自然科学基金(52293380)

国家自然科学基金(52293383)

Startup Fund of Wenzhou Institute,University of Chinese Academy of Sciences(WIUCASQD2021022)

Startup Fund of Wenzhou Institute,University of Chinese Academy of Sciences(WIUCASQD2021019)

出版年

2024
高分子科学(英文版)
中国化学会 中国科学院化学研究所

高分子科学(英文版)

CSTPCDCSCD
影响因子:0.721
ISSN:0256-7679
参考文献量49
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