Repository logo

Infoscience

  • English
  • French
Log In
Logo EPFL, École polytechnique fédérale de Lausanne

Infoscience

  • English
  • French
Log In
  1. Home
  2. Academic and Research Output
  3. Journal articles
  4. Spectroscopic studies of photobleaching and photoproduct formation of meta(tetrahydroxyphenyl)chlorin (m-THPC) used in photodynamic therapy. The production of singlet oxygen by m-THPC
 
research article

Spectroscopic studies of photobleaching and photoproduct formation of meta(tetrahydroxyphenyl)chlorin (m-THPC) used in photodynamic therapy. The production of singlet oxygen by m-THPC

Hadjur, Christophe
•
Lange, Norbert
•
Rebstein, Julia
Show more
1998
Journal of Photochemistry and Photobiology B: Biology

Meta(tetrahydroxyphenyl)chlorin (m-THPC) is a new photosensitizer currently undergoing clin. trials at Lausanne's CHUV hospital for photodynamic therapy (PDT) of early cancer in the upper aerodigestive tract. The illumination of m-THPC with light at 650 nm in aq. soln. contg. 10% fetal calf serum (FCS) causes two simultaneously occurring processes: its photodegrdn. and the formation of a more stable photoproduct absorbing at 320 nm. The photodegrdn. quantum yield (FPb) of m-THPC is found to be of the order of 1.510-5 in 10% FCS. A strong dependence on oxygen concn. of the photodegrdn. and the formation of photoproducts has been obsd. Indeed, the m-THPC presents rather low FPb under N2-satd. conditions: 6.910-6. In aerobic conditions, the photodegrdn. as well as the formation of photoproducts, have been competitively inhibited by known singlet oxygen (1O2) quenchers. The addn. of superoxide dismutase (SOD), catalase or desferal, known quenching agents of type I mechanisms, has little or no effect on the rate of photobleaching and photoproduct formation of m-THPC. m-THPC generates 1O2 with a quantum yield of 0.3 in ethanol soln. as detd. by photo-oxidn. expts. using 1,3-diphenylisobenzofuran (DPBF) as substrate. The rate and quantum yield of DPBF photo-oxidn. are found to increase with increasing substrate concn. and decrease in phosphate buffer soln. (FD=0.01), due to the partially hydrophilic character of m-THPC. In addn., the reaction of 1O2 with TEMP (2,2,6,6-tetramethyl-4-piperidone) in combination with ESR (EPR) detection has been used to det. the formation of 1O2 by m-THPC in ethanol soln.

  • Details
  • Metrics
Type
research article
DOI
10.1016/S1011-1344(98)00177-8
Web of Science ID

WOS:000077724500013

Author(s)
Hadjur, Christophe
Lange, Norbert
Rebstein, Julia
Monnier, Philippe
van den Bergh, Hubert  
Wagnières, Georges  
Date Issued

1998

Publisher

Elsevier

Published in
Journal of Photochemistry and Photobiology B: Biology
Volume

45

Issue

2-3

Start page

170

End page

178

Note

Antioxidants; Radical scavengers (photobleaching and photoproduct formation of m-THPC used in photodynamic therapy: effect of antioxidants and radical quenchers); Blood serum; Simulation and Modeling (photobleaching and photoproduct formation of m-THPC used in photodynamic therapy: effect of fetal calf serum); Oxidation; Photodynamic action; Photolysis; Photosensitizers (photobleaching and photoproduct formation of m-THPC used in photodynamic therapy: prodn. of singlet oxygen); Reactive oxygen species Role: BSU (Biological study, unclassified), BIOL (Biological study) (photobleaching and photoproduct formation of m-THPC used in photodynamic therapy: role of reactive oxygen species)

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LPAS  
Available on Infoscience
July 20, 2007
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/9619
Logo EPFL, École polytechnique fédérale de Lausanne
  • Contact
  • infoscience@epfl.ch

  • Follow us on Facebook
  • Follow us on Instagram
  • Follow us on LinkedIn
  • Follow us on X
  • Follow us on Youtube
AccessibilityLegal noticePrivacy policyCookie settingsEnd User AgreementGet helpFeedback

Infoscience is a service managed and provided by the Library and IT Services of EPFL. © EPFL, tous droits réservés