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Porphyrin distribution after topical aminolevulinic acid in a novel porcine model of sebaceous skin
Author(s) -
Sakamoto Fernanda H.,
Tannous Zeina,
Doukas Apostolos G.,
Farinelli William A.,
Smith Nicholas A.,
Zurakowski David,
Anderson R. Rox
Publication year - 2009
Publication title -
lasers in surgery and medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.888
H-Index - 112
eISSN - 1096-9101
pISSN - 0196-8092
DOI - 10.1002/lsm.20734
Subject(s) - epidermis (zoology) , photodynamic therapy , fluorescence , sebaceous gland , porphyrin , fluorescence microscope , in vivo , biodistribution , chemistry , human skin , pathology , anatomy , medicine , biology , in vitro , biochemistry , physics , genetics , microbiology and biotechnology , organic chemistry , quantum mechanics
Background and Objective Aminolevulinic acid photodynamic therapy (ALA‐PDT) depends on drug metabolism into porphyrins. Clinically, ALA‐PDT has been used with a wide range of protocols for treating both epidermal and dermal targets, despite limited understanding of porphyrin biodistribution over time. We studied porphyrin accumulation after topical application of ALA in vivo, and also describe the porcine ear as a new animal model to study adnexal glands. Study Design/Materials and Methods The microanatomy of anterior ear skin of swine was measured. Topical 20% ALA in water/ethanol was applied under occlusion. Biopsies taken after 5, 10, 15, and then every 15 minutes for a total of 3 hours were examined by fluorescence microscopy of frozen sections to assess accumulation and distribution of porphyrins. Results Porphyrin fluorescence of digital photomicrograph images was not visually apparent until 30–45 minutes after application, although quantitative pixel analysis showed a statistically significant increase in epidermal fluorescence only 15 minutes after ALA application. From 30 to 120 minutes, epidermis, hair follicles (HF), and sebaceous glands (SG) became progressively more fluorescent. Eccrine gland fluorescence began to be detected after 30 minutes; SG showed fluorescence starting at 45–75 minutes. Fluorescence in all sites reached maximum intensity from 75 to 180 minutes of incubation. There was a trend for HF and SG to express stronger fluorescence compared with epidermis and eccrine glands. Conclusion Anterior pig ear skin is microanatomically similar to human sebaceous skin. The time‐dependent accumulation of porphyrins in pilosebaceous units and eccrine glands in this model suggests other routes of uptake of topical ALA in addition to the trans‐epidermal route. Apparently, time interval between ALA application and light exposure could be optimized for different uses of ALA‐PDT. Lasers Surg. Med. 41:154–160, 2009. © 2009 Wiley‐Liss, Inc.