Fundamentals of fractional laser-assisted drug delivery: An in-depth guide to experimental methodology and data interpretation

被引:59
|
作者
Wenande, Emily [1 ,2 ]
Anderson, R. Rox [2 ]
Haedersdal, Merete [1 ,2 ]
机构
[1] Univ Copenhagen, Bispebjerg Hosp, Dept Dermatol, DK-2400 Copenhagen NV, Denmark
[2] Harvard Med Sch, Wellman Ctr Photomed, Massachusetts Gen Hosp, Boston, MA 02114 USA
关键词
Ablative fractional laser; Topical laser-assisted drug delivery; Skin absorption; In Vitro In Vivo models; Transdermal delivery; Physical enhancement strategies; Microporation; Microchannel morphology; barrier permeability; CARBON-DIOXIDE LASER; UNDERLYING TISSUE PHARMACOKINETICS; MEDIATED PHOTODYNAMIC THERAPY; BASAL-CELL CARCINOMA; TRANSDERMAL DELIVERY; PERCUTANEOUS-ABSORPTION; METHYL AMINOLEVULINATE; TOPICAL APPLICATION; SKIN PENETRATION; ERBIUMYAG LASER;
D O I
10.1016/j.addr.2019.10.003
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In the decade since their advent, ablative fractional lasers have emerged as powerful tools to enhance drug delivery to and through the skin. Effective and highly customizable, laser-assisted drug delivery (LADD) has led to improved therapeutic outcomes for several medical indications. However, for LADD to reach maturity as a standard treatment technique, a greater appreciation of its underlying science is needed. This work aims to provide an indepth guide to the technology's fundamental principles, experimental methodology and unique aspects of LADD data interpretation. We show that drug's physicochemical properties including solubility, molecular weight and tissue binding behavior, are crucial determinants of how laser channel morphology influences topical delivery. Furthermore, we identify strengths and limitations of experimental models and drug detection techniques, interrogating the usefulness of in vitro data in predicting LADD in vivo. By compiling insights from over 75 studies, we ultimately devise an approach for intelligent application of LADD, supporting its implementation in the clinical setting. (c) 2019 Elsevier B.V. All rights reserved.
引用
收藏
页码:169 / 184
页数:16
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