Lieckfeldt R, Villalain J, Gomez-Fernandez J C, Lee G
Institute for Pharmaceutical Technology and Biopharmaceutics, Heidelberg University, Germany.
Biochim Biophys Acta. 1993 Aug 15;1150(2):182-8. doi: 10.1016/0005-2736(93)90088-h.
Mixtures of model stratum corneum lipids were prepared in water from cholesterol, six fatty acids and ceramides. The influence of composition on the polymorphism of these mixtures and also on the diffusivity of a model drug within them, Dlip, was determined. The former was obtained from X-ray diffraction and Fourier transform infrared spectrometry, and the latter from a diffusional release model. An L beta structure was formed for the composition approximating that of the extracellular lipids in intact human abdominal stratum corneum. Dlip was independent of water content in the range 20-40% w/w, with the bilayers showing one dimensional swelling without lateral expansion. Although removal of the ceramides did not result in a significant alteration in Dlip, crystalline cholesterol now appeared. The ceramides were, therefore, necessary for solubilization within the fatty acid bilayers of the large proportion of cholesterol present in the lipid fraction of intact SC. They were also responsible for a thermal L alpha-HII transition observed at approx. 68 degrees. At the concentration in which it exists in intact SC, cholesterol also had only a minimal effect on Dlip, but was necessary to suppress HII phase formation within the fatty acids and ensure an L beta structure. All lipid mixtures that had an L beta structure presented a diffusional barrier approx. 1 order of magnitude greater than that of an unstructured, isotropic lipid mixture. HII structures formed at cholesterol/fatty acid proportions less than approx 8:92 mol% and appeared more permeable than L beta ones. All the results indicate that the diffusional barrier within the model lipid mixtures is guaranteed essentially by the presence of an L beta phase. Although the ceramides and cholesterol exert no intrinsic influence on the magnitude of Dlip, their presence in necessary for the existence of an L beta phase at 33 degrees that is free of both crystalline cholesterol and HII character.
由胆固醇、六种脂肪酸和神经酰胺在水中制备了模型角质层脂质混合物。确定了组成对这些混合物多晶型性以及模型药物在其中的扩散系数Dlip的影响。前者通过X射线衍射和傅里叶变换红外光谱法获得,后者通过扩散释放模型获得。对于接近完整人腹部角质层细胞外脂质组成的混合物,形成了Lβ结构。在20 - 40% w/w的含水量范围内,Dlip与含水量无关,双层显示出一维膨胀而无横向扩展。尽管去除神经酰胺不会导致Dlip发生显著变化,但现在出现了结晶胆固醇。因此,神经酰胺对于完整皮肤脂质部分中大量存在的胆固醇在脂肪酸双层中的溶解是必要的。它们还导致了在约68℃观察到的热Lα - HII转变。在完整皮肤中存在的浓度下,胆固醇对Dlip也只有最小的影响,但对于抑制脂肪酸内HII相的形成并确保Lβ结构是必要的。所有具有Lβ结构的脂质混合物呈现出的扩散屏障比无结构的各向同性脂质混合物大约高1个数量级。在胆固醇/脂肪酸比例小于约8:92 mol%时形成的HII结构似乎比Lβ结构更具渗透性。所有结果表明,模型脂质混合物中的扩散屏障基本上由Lβ相的存在来保证。尽管神经酰胺和胆固醇对Dlip的大小没有内在影响,但它们的存在对于在33℃存在不含结晶胆固醇和HII特征的Lβ相是必要的。