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Real-time luminescence microspectroscopy monitoring of singlet oxygen in individual cells
M. Scholz, R. Dědic, J. Valenta, T. Breitenbach, J. Hála,
Jazyk angličtina Země Anglie, Velká Británie
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
24954013
DOI
10.1039/c4pp00121d
Knihovny.cz E-zdroje
- MeSH
- analýza jednotlivých buněk přístrojové vybavení metody MeSH
- buňky 3T3 MeSH
- fibroblasty metabolismus MeSH
- fotochemické procesy MeSH
- fotosenzibilizující látky MeSH
- luminiscence MeSH
- mikrospektrofotometrie přístrojové vybavení metody MeSH
- myši MeSH
- počítačové systémy MeSH
- porfyriny MeSH
- singletový kyslík metabolismus MeSH
- zvířata MeSH
- Check Tag
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
A new setup for direct microspectroscopic monitoring of singlet oxygen ((1)O2) has been developed in our laboratory using a novel near-infrared sensitive InGaAs 2D-array detector. An imaging spectrograph has been inserted in front of the 2D-array detector, which allows us to acquire spectral images where one dimension is spatial and the other is spectral. The work presents a detailed examination of sensitivity and noise characteristics of the setup and its ability to detect (1)O2. The (1)O2 phosphorescence-based images and near-infrared luminescence spectral images recorded from single TMPyP-containing fibroblast cells reflecting spectral changes during irradiation are demonstrated. The introduction of spectral images addresses the issue of a potential spectral overlap of (1)O2 phosphorescence with near-infrared-extended luminescence of the photosensitizer and provides a powerful tool for distinguishing and separating them, which can be applied to any photosensitizer manifesting near-infrared luminescence.
Citace poskytuje Crossref.org
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