Photo-responsive membrane surface: Switching from bactericidal to bacteria-resistant property
In this paper, a photo-responsive bactericidal and bacteria-resistant membrane was successfully prepared via the integration of atom transfer radical polymerization (ATRP) and click chemistry. Azide-functionalized polycationic poly (N, N-dimethyl-N-(2-(methacryloyloxy)ethyl)-N-((2-nitrobenzyl)oxy)-2...
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Published in | Materials Science & Engineering C Vol. 84; pp. 52 - 59 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Netherlands
Elsevier B.V
01.03.2018
Elsevier BV |
Subjects | |
Online Access | Get full text |
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Summary: | In this paper, a photo-responsive bactericidal and bacteria-resistant membrane was successfully prepared via the integration of atom transfer radical polymerization (ATRP) and click chemistry. Azide-functionalized polycationic poly (N, N-dimethyl-N-(2-(methacryloyloxy)ethyl)-N-((2-nitrobenzyl)oxy)-2-oxoethanaminium bromide) (PDMAEMA-NBE) was synthesized by ATRP. Then, the PDMAEMA-NBE was clicked on alkynyl-functionalized polyethersulfone (PES) membrane surface, and proved by X-ray photoelectron spectrometer (XPS). Upon UV irradiation, the polycationic surface would switch to polyzwitterionic one. Before and after the irradiation, the zeta potentials of the surface altered from +14.7 to −3.8mV, and the water contact angle decreased from 64.0° to 52.7°. The polycationic surface exhibited excellent bactericidal property and the dead bacteria could detach from the polyzwitterionic surface induced by the subsequent UV irradiation. It demonstrated that the designing of photo-responsive membrane surface could be a new strategy for antibacterial adhesion.
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•Membranes surface were modified by combining ATRP and click chemistry.•Photo-induced membrane surface potential changed.•Switching from antibacterial to bacteria-resistant membrane surface. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0928-4931 1873-0191 |
DOI: | 10.1016/j.msec.2017.11.036 |