Nanoparticles for skin penetration enhancement - A comparison of a dendritic core-multishell-nanotransporter and solid lipid nanoparticles

被引:177
作者
Kuechler, Sarah [1 ]
Radowski, Michal R. [2 ]
Blaschke, Tobias [3 ]
Dathe, Margitta [4 ]
Plendl, Johanna [5 ]
Haag, Rainer [2 ]
Schaefer-Korting, Monila [1 ]
Kramer, Klaus D. [3 ]
机构
[1] Free Univ Berlin, Inst Pharm, D-14195 Berlin, Germany
[2] Free Univ Berlin, Inst Chem & Biocchem, D-14195 Berlin, Germany
[3] Free Univ Berlin, Inst Phys, D-14195 Berlin, Germany
[4] Leibniz Inst Mol Pharmacol, Berlin, Germany
[5] Free Univ Berlin, Inst Vet Anat, D-14195 Berlin, Germany
关键词
Dendritic core-multishell nanotransporters; Solid lipid nanoparticles; Skin penetration; Cellular uptake; Nile red; DRUG-DELIVERY SYSTEMS; ENCAPSULATING SILVER SULFADIAZINE; RECONSTRUCTED HUMAN EPIDERMIS; CULTURED HUMAN KERATINOCYTES; PARELECTRIC SPECTROSCOPY; TOPICAL DELIVERY; CARRIER SYSTEMS; CELLS; LIPOSOMES; SLN;
D O I
10.1016/j.ejpb.2008.08.019
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Nanosized particles are of growing interest for topical treatment of skin diseases to increase skin penetration of drugs and to reduce side effects. Effects of the particle structure and size were studied loading nile red to dendritic core-multishell (CMS) nanotransporters (20-30 nm) and solid lipid nanoparticles (SLNs, 150-170 nm). Interaction properties of CMS nanotransporters with the dye molecules - attachment to the carrier surface or incorporation in the carrier matrix - were studied by UV/Vis and parelectric spectroscopy. Pig skin penetration was studied ex vivo using a cream for reference. Interactions of SLN and skin were followed by scanning electron microscopy, internalisation of the particles by viable keratinocytes by laser scanning microscopy. Incorporating nile red into a stable dendritic nanoparticle matrix, dye amounts increased eightfold in the stratum corneum and 13-fold in the epidermis compared to the cream. Despite SLN degradation at the stratum corneum surface, SLN enhanced skin penetration less efficiently (3.8- and 6.3-fold). Viable human keratinocytes showed an internalisation of both nanocarriers. In conclusion, CMS nanotransporters can favour the penetration of a model dye into the skin even more than SLN which may reflect size effects. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:243 / 250
页数:8
相关论文
共 50 条
[1]
Enhancement of topical delivery from biodegradable nanoparticles [J].
Alvarez-Román, R ;
Naik, A ;
Kalia, YN ;
Guy, RH ;
Fessi, H .
PHARMACEUTICAL RESEARCH, 2004, 21 (10) :1818-1825
[2]
Skin penetration and distribution of polymeric nanoparticles [J].
Alvarez-Román, R ;
Naik, A ;
Kalia, Y ;
Guy, RH ;
Fessi, H .
JOURNAL OF CONTROLLED RELEASE, 2004, 99 (01) :53-62
[3]
Structure and dynamics of drug-carrier systems as studied by parelectric spectroscopy [J].
Blaschke, T. ;
Kankate, L. ;
Kramer, K. D. .
ADVANCED DRUG DELIVERY REVIEWS, 2007, 59 (06) :403-410
[4]
Lipid nanoparticles for skin penetration enhancement-correlation to drug localization within the particle matrix as determined by fluorescence and parelectric spectroscopy [J].
Borgia, SL ;
Regehly, M ;
Sivaramakrishnan, R ;
Mehnert, W ;
Korting, HC ;
Danker, K ;
Röder, B ;
Kramer, KD ;
Schäfer-Korting, M .
JOURNAL OF CONTROLLED RELEASE, 2005, 110 (01) :151-163
[5]
Skin structure and mode of action of vesicles [J].
Bouwstra, JA ;
Honeywell-Nguyen, PL .
ADVANCED DRUG DELIVERY REVIEWS, 2002, 54 :S41-S55
[6]
Interaction of drug molecules with carrier systems as studied by parelectric spectroscopy and electron spin resonance [J].
Braem, C. ;
Blaschke, T. ;
Panek-Minkin, G. ;
Herrmann, W. ;
Schlupp, P. ;
Paepenmueller, T. ;
Mueller-Goyman, C. ;
Mehnert, W. ;
Bittl, R. ;
Schaefer-Korting, M. ;
Kramer, K. D. .
JOURNAL OF CONTROLLED RELEASE, 2007, 119 (01) :128-135
[7]
Lipid vesicles and other colloids as drug carriers on the skin [J].
Cevc, G .
ADVANCED DRUG DELIVERY REVIEWS, 2004, 56 (05) :675-711
[8]
Liposomes and niosomes as topical drug delivery systems [J].
Choi, MJ ;
Maibach, HI .
SKIN PHARMACOLOGY AND PHYSIOLOGY, 2005, 18 (05) :209-219
[9]
CLARKE BL, 1985, J BIOL CHEM, V260, P128
[10]
Detection of nanometer-sized particles in living cells using modern fluorescence fluctuation methods [J].
Edetsberger, M ;
Gaubitzer, E ;
Valic, E ;
Waigmann, E ;
Köhler, G .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2005, 332 (01) :109-116