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Pretreatment with ablative fractional laser changes kinetics and biodistribution of topical 5‐aminolevulinic acid (ALA) and methyl aminolevulinate (MAL)
Author(s) -
Haedersdal Merete,
Sakamoto Fernanda H.,
Farinelli William A.,
Doukas Apostolos G.,
Tam Joshua,
Anderson R. Rox
Publication year - 2014
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.22259
Subject(s) - fluorescence , porphyrin , biodistribution , kinetics , photodynamic therapy , chemistry , photosensitizer , photochemistry , biochemistry , organic chemistry , in vitro , optics , physics , quantum mechanics
Background and Objectives 5‐Aminolevulinic acid (ALA) and methyl aminolevulinate (MAL) are porphyrin precursors used topically for photodynamic therapy (PDT). Previous studies have established that ablative fractional laser (AFXL) increases topical drug uptake. We evaluated kinetics and biodistribution of ALA‐ and MAL‐induced porphyrins on intact and disrupted skin due to AFXL. Materials and Methods Two Yorkshire swine were exposed to CO 2 AFXL (10.6 µm, 1,850 µm ablation depth) and subsequent topical application of ALA and MAL cream formulations (20%, weight/weight). Porphyrin fluorescence was quantified by digital fluorescence photography (30, 90, and 180 minutes) and fluorescence microscopy at specific skin depths (180 minutes). Results Porphyrins gradually formed over time, differently on intact and AFXL‐disrupted skin. On intact skin (no AFXL), fluorescence photography showed that MAL initially induced higher fluorescence than ALA ( t = 30 minutes MAL 21.1 vs. ALA 7.7 au, t = 90 minutes MAL 39.0 vs. ALA 26.6 ( P < 0.009)) but reached similar intensities for long‐term applications ( t = 180 minutes MAL 56.6 vs. ALA 52 au, P = ns). AFXL considerably enhanced porphyrin fluorescence from both photosensitizers ( P < 0.05). On AFXL‐exposed skin , MAL expressed higher fluorescence than ALA for short‐term application ( t = 30 minutes, AFXL–MAL 26.4 vs. AFXL–ALA 14.1 au, P < 0.001), whereas ALA over time overcame MAL and induced the highest fluorescence intensities obtained ( t = 180 minutes, AFXL–MAL 98.6 vs. AFXL–ALA 112.0 au, P < 0.001). In deep skin layers, fluorescence microscopy showed higher fluorescence in hair follicle epithelium for ALA than MAL ( t = 180 minutes, 1.8 mm, AFXL–MAL 35.3 vs. AFXL–ALA 46.7 au, P < 0.05). Conclusions AFXL changes kinetics and biodistribution of ALA and MAL. It appears that AFXL–ALA favors targeting deep structures. Lasers Surg. Med. 46:462–469, 2014. © 2014 Wiley Periodicals, Inc.