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Self-Assembled Borneol-Guanidine-Based Amphiphilic Polymers as an Efficient Antibiofilm Agent.
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- Additional Information
- Source:
Publisher: American Chemical Society Country of Publication: United States NLM ID: 101504991 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1944-8252 (Electronic) Linking ISSN: 19448244 NLM ISO Abbreviation: ACS Appl Mater Interfaces Subsets: MEDLINE
- Publication Information:
Original Publication: Washington, D.C. : American Chemical Society
- Subject Terms:
- Abstract:
Biofilm-associated infections remain a tremendous obstacle to the treatment of microbial infections globally. However, the poor penetrability to a dense extracellular polymeric substance matrix of traditional antibacterial agents limits their antibiofilm activity. Here, we show that nanoaggregates formed by self-assembly of amphiphilic borneol-guanidine-based cationic polymers (BGN x - n ) possess strong antibacterial activity and can eliminate mature Staphylococcus aureus ( S. aureus ) biofilms. The introduction of the guanidine moiety improves the hydrophilicity and membrane penetrability of BGN x - n . The self-assembled nanoaggregates with highly localized positive charges are expected to enhance their interaction with negatively charged bacteria and biofilms. Furthermore, nanoaggregates dissociate on the surface of biofilms into smaller BGN x - n polymers, which enhances their ability to penetrate biofilms. BGN x - n nanoaggregates that exhibit superior antibacterial activity have the minimum inhibitory concentration (MIC) of 62.5 μg·mL -1 against S. aureus and eradicate mature biofilms at 4 × MIC with negligible hemolysis. Taken together, this size-variable self-assembly system offers a promising strategy for the development of effective antibiofilm agents.
- Contributed Indexing:
Keywords: (+)-borneol; biofilm; guanidine; natural products; self-assembly
- Accession Number:
0 (Anti-Bacterial Agents)
JU58VJ6Y3B (Guanidine)
0 (Camphanes)
0 (Polymers)
L88RA8N5EG (isoborneol)
0 (Surface-Active Agents)
- Publication Date:
Date Created: 20240629 Date Completed: 20240725 Latest Revision: 20240725
- Publication Date:
20240726
- Accession Number:
10.1021/acsami.4c02818
- Accession Number:
38943568
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