A main chain biodegradable polyurethane with anti-protein adsorption and anti-bacterial adhesion performances

Biofilms are initially formed by substances such as proteins secreted by bacteria adhering to a surface. To achieve a durable antibacterial material, biodegradable dihydroxyl-terminated poly[(ethylene oxide)- co -(ethylene carbonate)] (PEOC(OH) 2 ) with anti-protein adsorption properties was synthes...

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Veröffentlicht in:Soft matter 2023-12, Vol.2 (1), p.192-2
Hauptverfasser: Cao, Zhonglin, Ma, Chunfeng, Xiang, Li, Cao, Linyan
Format: Artikel
Sprache:eng
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Zusammenfassung:Biofilms are initially formed by substances such as proteins secreted by bacteria adhering to a surface. To achieve a durable antibacterial material, biodegradable dihydroxyl-terminated poly[(ethylene oxide)- co -(ethylene carbonate)] (PEOC(OH) 2 ) with anti-protein adsorption properties was synthesized in this study. Further polycondensation of PEOC(OH) 2 and isophorone diisocyanate (IPDI) led to biodegradable polyurethane (PEOC-PU) with PEOC as the soft segment. For comparison, polyurethanes with polyethylene glycol (PEG-PU) and polypropylene glycol (PPG-PU) as soft segments were also synthesized. The chemical structures of the polyurethanes were characterized by 1 H NMR and FTIR. The biodegradation behavior of PEOC-PU promoted by lipase due to the presence of ethylene carbonate units was also studied. Their resistance to proteins was studied using quartz crystal microbalance with dissipation (QCM-D) and the results revealed that PEOC-PU exhibited excellent nonspecific resistance to proteins. The colonization of microorganisms on PU in the liquid culture medium was further examined and the results showed that PEOC-PU exhibited excellent antibacterial adhesion performance due to its protein resistance and biodegradation. A biodegradable PEOC-PU coating, a self-renewable material, presented outstanding nonspecific resistance to proteins and antibacterial adhesion, and could be hopefully used in medical antibacterial dressings.
ISSN:1744-683X
1744-6848
DOI:10.1039/d3sm01344h