Preparation of a New Oligolamellar Stratum Corneum Lipid Model

In this study, we present a preparation method for a new stratum corneum (SC) model system, which is closer to natural SC than the commonly used multilayer models. The complex setup of the native SC lipid matrix was mimicked by a ternary lipid mixture of ceramide [AP], cholesterol, and stearic acid....

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Published inLangmuir Vol. 32; no. 18; pp. 4673 - 4680
Main Authors Mueller, Josefin, Schroeter, Annett, Steitz, Roland, Trapp, Marcus, Neubert, Reinhard H. H
Format Journal Article
LanguageEnglish
Published United States American Chemical Society 10.05.2016
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Abstract In this study, we present a preparation method for a new stratum corneum (SC) model system, which is closer to natural SC than the commonly used multilayer models. The complex setup of the native SC lipid matrix was mimicked by a ternary lipid mixture of ceramide [AP], cholesterol, and stearic acid. A spin coating procedure was applied to realize oligo-layered samples. The influence of lipid concentration, rotation speed, polyethylenimine, methanol content, cholesterol fraction, and annealing on the molecular arrangement of the new SC model was investigated by X-ray reflectivity measurements. The new oligo-SC model is closer to native SC in the total number of lipid membranes found between corneocytes. The reduction in thickness provides the opportunity to study the effects of drugs and/or hydrophilic penetration enhancers on the structure of SC in full detail by X-ray or neutron reflectivity. In addition, the oligo-lamellar systems allows one to infer not only the lamellar spacing, but also the total thickness of the oligo-SC model and changes thereof can be monitored. This improvement is most helpful for the understanding of transdermal drug administration on the nanoscale. The results are compared to the commonly used multilamellar lipid model systems and advantages and disadvantages of both models are discussed.
AbstractList In this study, we present a preparation method for a new stratum corneum (SC) model system, which is closer to natural SC than the commonly used multilayer models. The complex setup of the native SC lipid matrix was mimicked by a ternary lipid mixture of ceramide [AP], cholesterol, and stearic acid. A spin coating procedure was applied to realize oligo-layered samples. The influence of lipid concentration, rotation speed, polyethylenimine, methanol content, cholesterol fraction, and annealing on the molecular arrangement of the new SC model was investigated by X-ray reflectivity measurements. The new oligo-SC model is closer to native SC in the total number of lipid membranes found between corneocytes. The reduction in thickness provides the opportunity to study the effects of drugs and/or hydrophilic penetration enhancers on the structure of SC in full detail by X-ray or neutron reflectivity. In addition, the oligo-lamellar systems allows one to infer not only the lamellar spacing, but also the total thickness of the oligo-SC model and changes thereof can be monitored. This improvement is most helpful for the understanding of transdermal drug administration on the nanoscale. The results are compared to the commonly used multilamellar lipid model systems and advantages and disadvantages of both models are discussed.
Author Steitz, Roland
Trapp, Marcus
Mueller, Josefin
Schroeter, Annett
Neubert, Reinhard H. H
AuthorAffiliation Martin Luther University
Institute of Soft Matter and Functional Materials
Helmholtz-Zentrum Berlin für Materialien und Energie GmbH
Institute of Pharmacy
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Snippet In this study, we present a preparation method for a new stratum corneum (SC) model system, which is closer to natural SC than the commonly used multilayer...
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SubjectTerms Biological and Environmental Phenomena at the Interface
Biomimetic Materials - chemistry
Cholesterol - chemistry
Epidermis - chemistry
Lipids - chemistry
Methanol - chemistry
Models, Molecular
Molecular Conformation
Spectroscopy, Fourier Transform Infrared
Title Preparation of a New Oligolamellar Stratum Corneum Lipid Model
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