Skip Navigation

This Article
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (15)
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Griffiths, M. A.
Right arrow Articles by Wilson, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Griffiths, M. A.
Right arrow Articles by Wilson, M.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Journal of Antimicrobial Chemotherapy, Vol 40, 873-876, Copyright © 1997 by The British Society for Antimicrobial Chemotherapy


ORIGINAL ARTICLES

Killing of methicillin-resistant Staphylococcus aureus in vitro using aluminium disulphonated phthalocyanine, a light-activated antimicrobial agent

MA Griffiths, BW Wren and M Wilson
Department of Microbiology, Eastman Dental Institute for Oral Health Care Sciences, University of London, UK.

The aim of this study was to determine whether 16 epidemic methicillin- resistant strains of Staphylococcus aureus (EMRSA) could be killed by the light-activated antimicrobial agent aluminium disulphonated phthalocyanine (AIPcS2). EMRSA suspensions were irradiated with light from a laser diode in the presence of AIPcS2 and survivors enumerated. All strains were susceptible to killing, the bactericidal effect being dependent on the AIPcS2 concentration and the light dose. AIPcS2 rendered the bacteria light-sensitive almost immediately and killing was unaffected by the growth phase of the organism. Scavengers of singlet oxygen and free radicals protected the bacteria from killing. These results imply that light-activated antimicrobial agents may be useful in eliminating EMRSA from wounds or carriage sites.
Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
J Antimicrob ChemotherHome page
C. K. Hope and M. Wilson
Induction of lethal photosensitization in biofilms using a confocal scanning laser as the excitation source
J. Antimicrob. Chemother., June 1, 2006; 57(6): 1227 - 1230.
[Abstract] [Full Text] [PDF]


Home page
J Antimicrob ChemotherHome page
S. Wood, D. Metcalf, D. Devine, and C. Robinson
Erythrosine is a potential photosensitizer for the photodynamic therapy of oral plaque biofilms
J. Antimicrob. Chemother., April 1, 2006; 57(4): 680 - 684.
[Abstract] [Full Text] [PDF]


Home page
Antimicrob. Agents Chemother.Home page
M. L. Embleton, S. P. Nair, W. Heywood, D. C. Menon, B. D. Cookson, and M. Wilson
Development of a Novel Targeting System for Lethal Photosensitization of Antibiotic-Resistant Strains of Staphylococcus aureus
Antimicrob. Agents Chemother., September 1, 2005; 49(9): 3690 - 3696.
[Abstract] [Full Text] [PDF]


Home page
Antimicrob. Agents Chemother.Home page
T. Maisch, C. Bosl, R.-M. Szeimies, N. Lehn, and C. Abels
Photodynamic Effects of Novel XF Porphyrin Derivatives on Prokaryotic and Eukaryotic Cells
Antimicrob. Agents Chemother., April 1, 2005; 49(4): 1542 - 1552.
[Abstract] [Full Text] [PDF]


Home page
J Antimicrob ChemotherHome page
M. L. Embleton, S. P. Nair, B. D. Cookson, and M. Wilson
Selective lethal photosensitization of methicillin-resistant Staphylococcus aureus using an IgG-tin (IV) chlorin e6 conjugate
J. Antimicrob. Chemother., December 1, 2002; 50(6): 857 - 864.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.