Abstract
Background and Objectives
Ablative fractional resurfacing (AFR) creates vertical channels that might assist the delivery of topically applied drugs into skin. The purpose of this study was to evaluate drug delivery by CO~2~ laser AFR using methyl 5‐aminolevulinate (MAL), a porphyrin precursor, as a test drug.
Materials and Methods
Two Yorkshire swine were treated with single‐hole CO~2~ laser AFR and subsequent topical application of MAL (Metvix®, Photocure ASA, Oslo, Norway), placebo cream and no drug. MAL‐induced porphyrin fluorescence was measured by fluorescence microscopy at skin depths down to 1,800 µm. AFR was performed with a 10.6 µm wavelength prototype CO~2~ laser, using stacked single pulses of 3 millisecond and 91.6 mJ per pulse.
Results
AFR created cone‐shaped channels of approximately 300 µm diameter and 1,850 µm depth that were surrounded by a 70 µm thin layer of thermally coagulated dermis. There was no porphyrin fluorescence in placebo cream or untreated skin sites. AFR followed by MAL application enhanced drug delivery with significantly higher porphyrin fluorescence of hair follicles (P<0.0011) and dermis (P<0.0433) versus MAL alone at skin depths of 120, 500, 1,000, 1,500, and 1,800 µm. AFR before MAL application also enhanced skin surface (epidermal) porphyrin fluorescence. Radial diffusion of MAL from the laser‐created channels into surrounding dermis was evidenced by uniform porphyrin fluorescence up to 1,500 µm from the holes (1,000, 1,800 µm depths). Skin massage after MAL application did not affect MAL‐induced porphyrin fluorescence after AFR.
Conclusions
Ablative fractional laser treatment facilitates delivery of topical MAL deeply into the skin. For the conditions of this study, laser channels approximately 3 mm apart followed by MAL application could produce porphyrins throughout essentially the entire skin. AFR appears to be a clinically practical means for enhancing uptake of MAL, a photodynamic therapy drug, and presumably many other topical skin medications. Lasers Surg. Med. 42:113–122, 2010. © 2009 Wiley‐Liss, Inc.