Rationally designed dual functional block copolymers for bottlebrush-like coatings: In vitro and in vivo antimicrobial, antibiofilm, and antifouling properties

被引:164
作者
Gao, Qiang [1 ]
Yu, Meng [1 ]
Su, Yajuan [1 ]
Xie, Meihua [1 ]
Zhao, Xin [1 ]
Li, Peng [2 ,3 ]
Ma, Peter X. [4 ,5 ,6 ,7 ]
机构
[1] Xi An Jiao Tong Univ, Ctr Biomed Engn & Regenerat Med, Frontier Inst Sci & Technol, Xian 710049, Peoples R China
[2] Nanjing Tech Univ, Jiangsu Natl Synerget Innovat Ctr Adv Mat SICAM, Key Lab Flexible Elect KLOFE, Nanjing 211816, Peoples R China
[3] Nanjing Tech Univ, Jiangsu Natl Synerget Innovat Ctr Adv Mat SICAM, Inst Adv Mat IAM, Nanjing 211816, Peoples R China
[4] Univ Michigan, Dept Biomed Engn, Ann Arbor, MI 48109 USA
[5] Univ Michigan, Dept Biol & Mat Sci, 1011,North Univ Ave,Room 2209, Ann Arbor, MI 48109 USA
[6] Univ Michigan, Macromol Sci & Engn Ctr, Ann Arbor, MI 48109 USA
[7] Univ Michigan, Dept Mat Sci & Engn, Ann Arbor, MI 48109 USA
关键词
Antimicrobial polypeptides; Surface coating; Antifouling; Antibiofilm; Polymer bottlebrush; RING-OPENING POLYMERIZATION; POLY(ETHYLENE GLYCOL); TITANIUM SURFACES; PEPTIDE MELIMINE; BROAD-SPECTRUM; ANTIBACTERIAL; INFECTION; SILICONE; BRUSH; ADSORPTION;
D O I
10.1016/j.actbio.2017.01.061
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
Numerous antimicrobial coatings have been developed for biomedical devices/implants, but few can simultaneously fulfill the requirements for antimicrobial and antifouling ability and biocompatibility. In this study, to develop an antimicrobial and antibiofilm surface coating, diblock amphiphilic molecules with antimicrobial and antifouling segments in a single chain were rationally designed and synthesized. Cationic antimicrobial polypeptides (AMP) were first synthesized by N-carboxyanhydride ring-opening polymerization (NCA-ROP). Heterofunctionalized poly(ethylene glycol) with different lengths (methacrylate-PEG(n)-tosyl, n = 10/45/90) was synthesized and site-specifically conjugated with polypeptides to form diblock amphiphiles. Along with increased PEG chain length, hemolytic activity was considerably improved, and broad-spectrum antimicrobial activity is retained. Three MA-PEGSb-AMP copolymers were further grafted onto the surface of silicone rubber (a commonly used catheter material) via plasma/UV-induced surface polymerizations to form a bottlebrush-like coating with excellent antimicrobial activity against several pathogenic bacteria (Escherichia coli, Pseudomonas aeruginosa, and Staphylococcus aureus), and effectively prevent biofilm formation. This bottlebrush coating also greatly reduced protein adsorption and platelet adhesion, indicating its excellent antifouling ability. An in vitro cytotoxicity study also demonstrated that this coating is biocompatible with mammalian cells. After subcutaneous implantation of the materials in rats, we demonstrated that the g-PEG(45)-b-AMP bottlebrush coating exhibits significant anti-infective activity in vivo. Thus, this facilely synthesized PEGylated AMP bottlebrush coating is a feasible method to prevent biomedical devices-associated infections. Statement of Significance Current antimicrobial coatings are often associated with concerns such as antibiotic resistance, environmental pollution, short-time antimicrobial activity, biofouling, poor blood compatibility and cytotoxicity, etc. To overcome these drawbacks, a robust PEGylated cationic amphiphilic peptides-based bottlebrushlike surface coating is demonstrated here, which fulfil the requirements of antimicrobial and antifouling as well as biocompatibility in the meantime. Briefly, the rational designed g-PEG(n)-b-AMP block copolymers (n = 10/45/90) were synthesized and grafted on silicone surface. This bottlebrush-like coating efficiently kill the contacted bacteria and prevent the biofilm formation, greatly reduced protein and platelet adhesion. It also exhibits excellent blood compatibility and low cytotoxicity in vitro. In particular, gPEG(45)-b-AMP coating exhibits significant anti-infection effect in vivo. This coating offering an effective strategy for combating biomedical devices-associated infections. (c) 2017 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:112 / 124
页数:13
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