Study of cyclic antibacterial polymers

The pervasiveness of microbial infections and the development of resistance in bacteria against traditional antibiotics have created a need for an alternative solution. Synthetic materials such as cationic cyclic Poly 2-(dimethylamino)ethyl methacrylate copolymerized with tert-butyl methacrylate P(D...

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Main Author: Sagar, Kundan Kumar
Other Authors: Duan Hongwei
Format: Theses and Dissertations
Language:English
Published: 2016
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Online Access:http://hdl.handle.net/10356/68443
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-684432023-03-03T16:02:16Z Study of cyclic antibacterial polymers Sagar, Kundan Kumar Duan Hongwei School of Chemical and Biomedical Engineering DRNTU::Engineering::Bioengineering The pervasiveness of microbial infections and the development of resistance in bacteria against traditional antibiotics have created a need for an alternative solution. Synthetic materials such as cationic cyclic Poly 2-(dimethylamino)ethyl methacrylate copolymerized with tert-butyl methacrylate P(DMAEMA-co-tBMA) are of interest due to the difficulty for bacteria to modify their entire cell membrane to develop resistance. This paper reports the successful synthesis of the cyclic and linear architectures of cationic P(DMAEMA-co-tBMA) to investigate and compare their respective antimicrobial properties. The two variants were polymerized utilizing ATRP and the cyclic structure was obtained via intra-chain ‘click’ cyclization. They were then characterized using nuclear magnetic resonance (NMR), Fourier transform infrared spectroscopy (FTIR) and size exclusion chromatography (SEC). The antimicrobial properties were tested using minimum inhibitory concentration (MIC) tests, live/dead assays and SEM to assess cell viability and effects that polymers have on Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) cell membranes. The MIC tests show that cyclic structures have superior antimicrobial effects in comparison to linear structures. In the case of E. coli, cyclic structures required 78 μg/ml MIC as compared to 156 μg/ml for linear and 40 μg/ml vs 78 μg/ml for S. aureus. This could be attributed to the smaller hydrodynamic diameter of cyclic probably due to self-assembly which condenses the cationic charges and increases electrostatic interactions with bacteria cell walls. ​Master of Science (Biomedical Engineering) 2016-05-26T02:39:14Z 2016-05-26T02:39:14Z 2016 Thesis http://hdl.handle.net/10356/68443 en 58 p. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic DRNTU::Engineering::Bioengineering
spellingShingle DRNTU::Engineering::Bioengineering
Sagar, Kundan Kumar
Study of cyclic antibacterial polymers
description The pervasiveness of microbial infections and the development of resistance in bacteria against traditional antibiotics have created a need for an alternative solution. Synthetic materials such as cationic cyclic Poly 2-(dimethylamino)ethyl methacrylate copolymerized with tert-butyl methacrylate P(DMAEMA-co-tBMA) are of interest due to the difficulty for bacteria to modify their entire cell membrane to develop resistance. This paper reports the successful synthesis of the cyclic and linear architectures of cationic P(DMAEMA-co-tBMA) to investigate and compare their respective antimicrobial properties. The two variants were polymerized utilizing ATRP and the cyclic structure was obtained via intra-chain ‘click’ cyclization. They were then characterized using nuclear magnetic resonance (NMR), Fourier transform infrared spectroscopy (FTIR) and size exclusion chromatography (SEC). The antimicrobial properties were tested using minimum inhibitory concentration (MIC) tests, live/dead assays and SEM to assess cell viability and effects that polymers have on Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) cell membranes. The MIC tests show that cyclic structures have superior antimicrobial effects in comparison to linear structures. In the case of E. coli, cyclic structures required 78 μg/ml MIC as compared to 156 μg/ml for linear and 40 μg/ml vs 78 μg/ml for S. aureus. This could be attributed to the smaller hydrodynamic diameter of cyclic probably due to self-assembly which condenses the cationic charges and increases electrostatic interactions with bacteria cell walls.
author2 Duan Hongwei
author_facet Duan Hongwei
Sagar, Kundan Kumar
format Theses and Dissertations
author Sagar, Kundan Kumar
author_sort Sagar, Kundan Kumar
title Study of cyclic antibacterial polymers
title_short Study of cyclic antibacterial polymers
title_full Study of cyclic antibacterial polymers
title_fullStr Study of cyclic antibacterial polymers
title_full_unstemmed Study of cyclic antibacterial polymers
title_sort study of cyclic antibacterial polymers
publishDate 2016
url http://hdl.handle.net/10356/68443
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