Applications and limitations of lipid nanoparticles in dermal and transdermal drug delivery via the follicular route

被引:104
作者
Lauterbach, Andreas [1 ]
Mueller-Goymann, Christel C. [1 ]
机构
[1] Tech Univ Carolo Wilhelmina Braunschweig, Inst Pharmazeut Technol, D-38106 Braunschweig, Germany
关键词
Lipid nanoparticle; Solid lipid nanoparticle; Nanolipid carrier; Hair follicle; Follicular penetration; Dermal drug delivery; Transdermal drug delivery; Sebum; Active pharmaceutical ingredient; Stratum corneum; SKIN PENETRATION ENHANCEMENT; TOPICALLY APPLIED SUBSTANCES; HAMSTER FLANK ORGAN; IN-VITRO PERMEATION; HAIR-FOLLICLES; EX-VIVO; PERCUTANEOUS-ABSORPTION; PILOSEBACEOUS UNIT; PHYSICAL STABILITY; STRATUM-CORNEUM;
D O I
10.1016/j.ejpb.2015.06.020
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Lipid nanoparticles (LN) such as solid lipid nanoparticles (SLN) and nanolipid carriers (NLC) feature several claimed benefits for topical drug therapy including biocompatible ingredients, drug release modification, adhesion to the skin, and film formation with subsequent hydration of the superficial skin layers. However, penetration and permeation into and across deeper skin layers are restricted due to the barrier function of the stratum corneum (SC). As different kinds of nanoparticles provide the potential for penetration into hair follicles (HF) LN are applicable drug delivery systems (DDS) for this route in order to enhance the dermal and transdermal bioavailability of active pharmaceutical ingredients (API). Therefore, this review addresses the HF as application site, published formulations of LN which showed follicular penetration (FP), and characterization methods in order to identify and quantify the accumulation of API delivered by the LN in the HF. Since LN are based on lipids that appear in human sebum which is the predominant medium in HF an increased localization of the colloidal carriers as well as a promoted drug release may be assumed. Therefore, sebum-like lipid material and a size of less or equal 640 nm are appropriate specifications for FP of particulate formulations. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:152 / 163
页数:12
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