Antibacterial activity and mechanism of piperazine polymer. Issue 20 (10th January 2021)

• Record Type: Journal Article
• Authors: Zhang, Maolan; Wang, Yuanliang; Zeng, Guoming; Yang, Shuang; Liao, Xiaoling; Sun, Da
• Is Part Of: Journal of applied polymer science. Volume 138:Issue 20(2021)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2021-01-10
• Subjects: antibacterial activity -- antibacterial mechanism -- piperazine polymer; Polymers -- Periodicals; Polymerization -- Periodicals; 668.9
• DOI: 10.1002/app.50451
• Languages: English
• ISSNs: 0021-8995

Abstract

Abstract: Piperazine polymers poly(ethylenediaminetetraacetic dianhydride‐co‐piperazine) (PE) and MGF‐Ct24E‐modified poly(ethylenediaminetetraacetic dianhydride‐co‐piperazine) (PEM) showed good antibacterial activity. Considering their different applications, the effects of time, pH, and inoculation concentration of these antibacterials against Escherichia coli ( E. coli ) in unique environments were evaluated in this study. The results indicated that the MIC and MBC values of the polymers increased after the introduction of MGF‐Ct24E into PE, but the two types of polymers still exhibited good antibacterial activity in a short time period under acidic conditions. In addition, we investigated the effect of the piperazine polymers on bacterial cell structure. It was clear that PE and PEM could destroy the bacterial cell wall, cell membrane and DNA, and their specific mechanism may be different. For PE, its carboxyl group could react with peptidoglycans on the E.coli cell wall to form holes on the bacterial surface, allowing PE to penetrate into the bacterial cell to damage DNA. For PEM, the alkaline MGF‐Ct24E could adsorb E.coli and make it shrink, meanwhile, the PE component created small holes on the bacterial walls and membranes, and inserted into the bacteria to result in bactericidal effect. These findings reveal the potential usefulness of PE and PEM in biomedical applications. Abstract : Piperazine polymers PE and PEM showed good antibacterial activity on E. coli and their specific mechanism were different. The carboxyl group of PE could react with peptidoglycans on the E.coli cell wall to form holes, allowing PE to penetrate into the bacterial cell to damage DNA. The MGF‐Ct24E in PEM could adsorb E.coli, then the PE component created small holes in bacterial cells and inserted into the bacterial to result in bactericidal effect.