Nontoxic, Hydrophilic Cationic Polymers-Identified as Class of Antimicrobial Polymers
Amphiphilic polycations are an alternative to biocides but also toxic to mammalian cells. Antimicrobially active hydrophilic polycations based on 1,4‐dibromo‐2‐butene and tetramethyl‐1,3‐propanediamine named PBI are not hemotoxic for porcine red blood cells with a hemocytotoxicity (HC50) of more tha...
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Published in: | Macromolecular bioscience Vol. 15; no. 12; pp. 1710 - 1723 |
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Main Authors: | , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Germany
Blackwell Publishing Ltd
01-12-2015
Wiley Subscription Services, Inc |
Subjects: | |
Online Access: | Get full text |
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Summary: | Amphiphilic polycations are an alternative to biocides but also toxic to mammalian cells. Antimicrobially active hydrophilic polycations based on 1,4‐dibromo‐2‐butene and tetramethyl‐1,3‐propanediamine named PBI are not hemotoxic for porcine red blood cells with a hemocytotoxicity (HC50) of more than 40 000 μg · mL−1. They are quickly killing bacterial cells at their MIC (minimal inhibitory concentration). The highest found selectivity HC50/MIC is more than 20 000 for S. epidermidis. Investigations on sequentially prepared PBIs with defined molecular weight Mn and tailored end groups revealed that there is a dependence of antimicrobial activity and selectivity on Mn and nature of the end groups.
Antimicrobially active and nontoxic hydrophilic polycations based on 1,4‐dibromo‐2‐butene and tetramethyl‐1,3‐propanediamine (PBI) are an alternative to toxic biocides and amphiphilic polycations. Investigations on PBIs with defined molecular weight (Mn) and tailored end groups revealed that there is a dependence of antimicrobial activity and selectivity on Mn and nature of the end groups. |
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Bibliography: | ark:/67375/WNG-R5LLBXQ3-W butcher shops Niemann and Vollmer istex:A09B84C0E1ED3F1FAB922778233C45604428C005 ArticleID:MABI201500207 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1616-5187 1616-5195 |
DOI: | 10.1002/mabi.201500207 |