Cited by 178Nonmelanoma Skin Cancer StudiesPhotodynamic Therapy Research StudiesPorphyrin Metabolism and Disorders

DISTRIBUTION OF 5‐AMINOLEVULINIC ACID‐INDUCED PORPHYRINS IN NODULOULCERATIVE BASAL CELL CARCINOMA

Peng, Qian, Warloe, Trond, Moan, Johan, Heyerdahl, Helen, Steen, Harald B., Nesland, Jahn M., Giercksky, Karl‐Erik·1995·Photochemistry and Photobiology

Abstract

Abstract— Microscopic fluorescence photometry incorporating a light‐sensitive thermo‐electrically cooled charge‐coupled device (CCD) camera was employed to investigate the fluorescence distribution of 5‐aminolevulinic acid (ALA)‐induced porphyrins in 22 patients with a total number of 52 noduloul‐cerative basal cell carcinomas (BCC) after topical ALA application with or without dimethylsulfoxide (DMSO)/ethylenediaminetetraacetic acid (EDTA) or after intravenous administration of ALA. Both localization patterns and amounts of ALA‐induced porphyrins in the BCC were studied. The ALA‐induced porphyrins were localized only in the superficial layers of the noduloulcerative BCC lesions after topical application of 20% ALA alone for 3 h. However, both the penetration of ALA into deep lesions and the production of the ALA‐induced porphyrin fluorescence were increased after topical administration of 20% ALA and 20% DMSO/4% EDTA for 3 h. Prior treatment with 99% DMSO for 15 min further enhanced the ALA penetration into the BCC lesions after topical application of the ALA/DMSO/EDTA mixture and produced more ALA‐induced porphyrins by a factor of about three compared with those treated with ALA alone. The penetration of ALA into the deep BCC lesions could also be increased by prolonging the time of topical application of 20% ALA/4% EDTA to 29–48 h (without DMSO). Intravenous injection of ALA led to a more homogeneous distribution of the ALA‐derived porphyrins in the whole noduloulcerative BCC lesions.

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Crossref · 10.1111/j.1751-1097.1995.tb09154.x

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  • EDTA does not increase PpIX production in a mouse tumor model and BCC patients after ALA administration, and DFO does not enhance PpIX fluorescence in skin cancer patients.

    “Despite these promising results from many in vitro studies, EDTA does not increase PpIX production in a mouse tumor model [102] and BCC patients [103] after ALA administration, and DFO does not enhance PpIX fluorescence in skin cancer patients either [104].”

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Authors
Peng, Q., Warloe, T., Moan, J., Heyerdahl, H., Steen, H. B., Nesland, J. M., & Giercksky, K.
Venue
Photochemistry and Photobiology
Publisher
Wiley
Published
1995-11
Volume
62
Issue
5
Pages
906-913
ISSN
  • 0031-8655 (ISSN-L)
  • 1751-1097
OpenAlex
W2100592740
Cited by
178
References
2
Citations by year
2025: 1 · 2024: 2 · 2023: 2 · 2022: 2 · 2019: 2 · 2017: 1 · 2016: 3 · 2015: 1 · 2014: 2 · 2013: 4 · 2012: 3
FWCI
9.68
Type
journal article
Language
en
Open access
closed
Locations
  • Photochemistry and Photobiology (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Epidemiology › Nonmelanoma Skin Cancer Studies
  • Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Photodynamic Therapy Research Studies
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Porphyrin Metabolism and Disorders
Keywords
5-aminolevulinic acid, porphyrins, topical photodynamic therapy, dimethyl sulfoxide, EDTA, fluorescence distribution, superficial skin lesions
MeSH terms
Adult, Aged, Aged, 80 and over, Aminolevulinic Acid, Carcinoma, Basal Cell, Basal Cell Carcinoma, Dimethyl Sulfoxide, Humans, Microscopy, Fluorescence, Middle Aged, Photochemotherapy, Porphyrins, Skin Neoplasms

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