Literature DB >> 31550124

Charge-Switchable Polymeric Coating Kills Bacteria and Prevents Biofilm Formation in Vivo.

Jiaul Hoque, Sreyan Ghosh, Krishnamoorthy Paramanandham1, Jayanta Haldar.   

Abstract

Preventing bacterial biofilm formation on medical devices and implants in vivo still remains a daunting task. Current antibacterial coatings to combat implant-associated infections are generally composed of toxic metals or nondegradable polymers and involve multistep surface modifications. Here, we present a charge-switchable antibacterial and antibiofilm coating based on water-insoluble cationic hydrophobic polymers that are soluble in organic solvents and can be noncovalently coated onto different surfaces. Toward this, a library of quaternary polyethylenimine (QPEI) polymers with an amide or ester group in their pendant alkyl chain was developed. These QPEIs are shown to hydrolyze from active cationic to nontoxic zwitterionic polymers under acidic or enzymatic conditions. Notably, polymers with both zwitterionic and cationic groups, obtained upon partial hydrolysis of QPEIs, are shown to retain their antibacterial activity with much lower toxicity toward mammalian cells. Furthermore, the zwitterionic polymer, a fully hydrolyzed product of the QPEIs, is shown to be nontoxic to mammalian cells in vitro as well as in vivo. The QPEIs, when coated onto surfaces, kill bacteria and prevent formation of biofilms. In an in vivo mice model, the QPEI-coated medical grade catheter is shown to reduce methicillin-resistant Staphylococcus aureus contamination both on the catheter surface and in the adjacent tissues (99.99% reduction compared to a noncoated catheter). Additionally, biofilm formation is inhibited on the catheter surface with negligible inflammation in the adjacent tissue. The above results thus highlight the importance of these polymers to be used as effective antibacterial coatings in biomedical applications.

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Keywords:  anti-infective biomaterials; antibiofilm activity; bactericidal coating; methicillin-resistant Staphylococcus aureus; side-chain hydrolysable polymers

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Year:  2019        PMID: 31550124     DOI: 10.1021/acsami.9b11453

Source DB:  PubMed          Journal:  ACS Appl Mater Interfaces        ISSN: 1944-8244            Impact factor:   9.229


  3 in total

1.  Erythrocyte membrane-camouflaged nanoworms with on-demand antibiotic release for eradicating biofilms using near-infrared irradiation.

Authors:  Luoxiao Ran; Bitao Lu; Haoyu Qiu; Guofang Zhou; Jing Jiang; Enling Hu; Fangyin Dai; Guangqian Lan
Journal:  Bioact Mater       Date:  2021-03-01

2.  Design Guidelines for Cationic Pillar[n]arenes that Prevent Biofilm Formation by Gram-Positive Pathogens.

Authors:  Dana Kaizerman-Kane; Maya Hadar; Roymon Joseph; Dana Logviniuk; Yossi Zafrani; Micha Fridman; Yoram Cohen
Journal:  ACS Infect Dis       Date:  2021-03-03       Impact factor: 5.084

Review 3.  Recent trends and advances in polyindole-based nanocomposites as potential antimicrobial agents: a mini review.

Authors:  Hareesh Pradeep; Bindu M; Shwetha Suresh; Anjitha Thadathil; Pradeepan Periyat
Journal:  RSC Adv       Date:  2022-03-15       Impact factor: 3.361

  3 in total

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