Abstract | OBJECTIVES: To induce lethal photosensitization in biofilms of Streptococcus pyogenes using the scanning laser in a confocal microscope to photoactivate Sn (IV) chlorin e6 ( SnCe6) while simultaneously measuring changes in cell vitality using fluorescent indicators of membrane integrity. METHODS: Biofilms of S. pyogenes were immersed in a solution of 50 mg/L (70.28 microM) SnCe6 and scanned with the 488 nm argon and 543 nm HeNe lasers in a confocal microscope. Changes in membrane permeability were quantified using image analysis tools. RESULTS: Cell permeability increased in biofilms of S. pyogenes after successive scanning/exposure cycles in the presence of SnCe6. CONCLUSIONS: Cell death was induced in biofilms of S. pyogenes by the photosensitizer SnCe6 on exposure to the scanning laser emissions of a confocal microscope. The simultaneous recording of cell death demonstrates the real-time evaluation of a light-activated antimicrobial compound against a biofilm.
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Authors | C K Hope, M Wilson |
Journal | The Journal of antimicrobial chemotherapy
(J Antimicrob Chemother)
Vol. 57
Issue 6
Pg. 1227-30
(Jun 2006)
ISSN: 0305-7453 [Print] England |
PMID | 16549510
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Anti-Bacterial Agents
- Fluorescent Dyes
- Metalloporphyrins
- Photosensitizing Agents
- tin(IV) chlorin e6
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Topics |
- Anti-Bacterial Agents
(pharmacology)
- Biofilms
(drug effects, growth & development)
- Cell Membrane
(pathology)
- Cell Membrane Permeability
(physiology)
- Fluorescent Dyes
(metabolism)
- Image Processing, Computer-Assisted
- Lasers
- Metalloporphyrins
(pharmacology)
- Photosensitizing Agents
(pharmacology)
- Streptococcus pyogenes
(drug effects, growth & development)
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