Semisolid SLN™ dispersions for topical application:: influence of formulation and production parameters on viscoelastic properties

被引:85
作者
Lippacher, A [1 ]
Müller, RH [1 ]
Mäder, K [1 ]
机构
[1] Free Univ Berlin, Dept Pharmaceut Biopharmaceut & Biotechnol, D-12169 Berlin, Germany
关键词
solid lipid nanoparticles; high pressure homogenization; rheology; oscillatory testing; topical applications; stability;
D O I
10.1016/S0939-6411(01)00233-8
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Aqueous solid lipid nanoparticle (SLN) dispersions with a high lipid Content Lip to 35% and viscous to semisolid consistency were produced by a high pressure homogenization process. Despite their high lipid content and viscosity these dispersions preserved their colloidal size range. The SLN dispersions were compared to nanoemulsions and microparticle dispersions with regard to particle size. viscoelastic properties and formation of a semisolid gel structure. Viscoelastic measurements including oscillation stress sweep tests and oscillation frequency sweep tests demonstrated that the existence of a solid particle matrix with a particle size in the nanometer range is a prerequisite to form a semisolid dispersion having the appropriate consistency for topical application. Striking differences were observed between solid lipid micro- and nanodispersions of the same composition, Particle size reduction resulted in an 80-fold increase of the elastic modulus, Particle size distribution, the physical state of the dispersed lipid phase and the emulsifier concentration have been identified as further key factors for the viscoelastic propertied and gel structure of the lipid nanodispersions. By conducting oscillation measurements it was possible to relate the stability of lipid dispersions to specific rheological parameters therefore providing a sensitive tool in stability assessment. Changing the production process from a 40 ml batch to a 21 batch turned out to have an influence on the colloidal structures of semisolid SLN dispersions. Consistency increased but particle size and ratio of elastic to viscous properties stayed in the same range. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:155 / 160
页数:6
相关论文
共 20 条
[1]  
[Anonymous], 1998, EUROCOSMETICS
[2]  
BORNFRIEND R, 1978, COSMET TOILETRIES, V93, P61
[3]  
BRICENO MI, 2000, PHARM EMULSIONS SUSP, P557
[4]   PREPARATION AND STRUCTURE OF A WATER-IN-OIL CREAM CONTAINING LIPID NANOPARTICLES [J].
DEVRINGER, T ;
DERONDE, HAG .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1995, 84 (04) :466-472
[5]  
Dingler A, 1999, J MICROENCAPSUL, V16, P751
[6]   MICROSTRUCTURAL CHANGES DURING THE STORAGE OF SYSTEMS CONTAINING CETOSTEARYL ALCOHOL POLYOXYETHYLENE ALKYL ETHER SURFACTANTS [J].
ECCLESTON, GM ;
BEATTIE, L .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 1988, 14 (15-17) :2499-2518
[7]   CORRELATION OF VISCOELASTIC FUNCTIONS FOR PHARMACEUTICAL SEMISOLIDS - COMPARISON OF CREEP AND OSCILLATORY TESTS FOR OIL-IN-WATER CREAMS STABILIZED BY MIXED EMULSIFIERS [J].
ECCLESTON, GM ;
BARRY, BW ;
DAVIS, SS .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1973, 62 (12) :1954-1961
[8]   Vitamin A loaded solid lipid nanoparticles for topical use:: occlusive properties and drug targeting to the upper skin [J].
Jenning, V ;
Gysler, A ;
Schäfer-Korting, M ;
Gohla, SH .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2000, 49 (03) :211-218
[9]   Characterisation of a novel solid lipid nanoparticle carrier system based on binary mixtures of liquid and solid lipids [J].
Jenning, V ;
Thünemann, AF ;
Gohla, SH .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2000, 199 (02) :167-177
[10]  
JENNING V, 1999, P INT S CONTROL REL, V26, P405