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PMID: 15571411 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Tuning the hemolytic and antibacterial activities of amphiphilic polynorbornene derivatives.

Journal of the American Chemical Society ·Vol. 126 ·No. 48 ·2004-12-08 ·Pages 15870-5

Ilker MF, Nüsslein K, Tew GN, Coughlin EB

Abstract

Amphiphilic cationic polynorbornene derivatives, soluble in water, were prepared from modular norbornene monomers, with a wide range of molecular weights (M(n) = 1600-137 500 g/mol) and narrow polydispersities (PDI = 1.1-1.3). The antibacterial activity determined by growth inhibition assays and the hemolytic activity against human red blood cells were measured and compared to determine the selectivity of the polymers for bacterial over mammalian cells. The effects of monomer repeat unit hydrophobicity and polymer molecular weight on antibacterial and hemolytic activities were determined. The hydrophobicity of the repeat unit was observed to have dramatic effects on antibacterial and hemolytic activities. Lipid membrane disruption activities of the polymers was confirmed by measuring polymer-induced dye leakage from large unilamellar vesicles. By tuning the overall hydrophobicity of the polymer through random copolymerizations of modular norbornene derivatives, highly selective, nonhemolytic antibacterial activities were obtained. For appropriate monomer composition, selectivity against bacteria versus human red blood cells was determined to be over 100.

MeSH Terms
Anti-Bacterial Agents/chemistry,pharmacology Bacillus subtilis/drug effects Cell Membrane/drug effects Cholesterol/chemistry Erythrocytes/drug effects Escherichia coli/drug effects Hemolysis Humans Liposomes/chemistry Microbial Sensitivity Tests Molecular Weight Norbornanes/chemistry,pharmacology Polymers/chemistry,pharmacology Structure-Activity Relationship
Chemicals
Anti-Bacterial Agents Liposomes Norbornanes Polymers Cholesterol
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Ilker M Firat
Department of Polymer Science and Engineering, University of Massachusetts Amherst, Amherst, Massachusetts 01003, USA.
Nüsslein Klaus
Tew Gregory N
Coughlin E Bryan
Article Info
Journal
Journal of the American Chemical Society
Abbr.
J Am Chem Soc
ISSN
0002-7863
Published
2004-12-08
Pages
15870-5
Language
English
Region
United States
NLM ID
7503056
Subset
IM
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