Uchiyama Masayuki, Oguri Masashi, Mojumdar Enamul H, Gooris Gert S, Bouwstra Joke A
Tokyo Research Laboratories, Kao Corporation, Bunka, Sumida-ku, Tokyo 131-8501, Japan; Leiden/Amsterdam Center for Drug Research, Department of Drug Delivery Technology, Leiden University, 2300 RA Leiden, The Netherlands.
Tochigi Research Laboratories, Kao Corporation, Ichikai, Haga, Tochigi 321-3497, Japan; Leiden/Amsterdam Center for Drug Research, Department of Drug Delivery Technology, Leiden University, 2300 RA Leiden, The Netherlands.
Biochim Biophys Acta. 2016 Sep;1858(9):2050-2059. doi: 10.1016/j.bbamem.2016.06.001. Epub 2016 Jun 7.
The lipid matrix in the stratum corneum (SC) plays an important role in the barrier function of the skin. The main lipid classes in this lipid matrix are ceramides (CERs), cholesterol (CHOL) and free fatty acids (FFAs). The aim of this study was to determine whether a variation in CER subclass composition and chain length distribution of FFAs affect the permeability of this matrix. To examine this, we make use of lipid model membranes, referred to as stratum corneum substitute (SCS). We prepared SCS containing i) single CER subclass with either a single FFA or a mixture of FFAs and CHOL, or ii) a mixture of various CER subclasses with either a single FFA or a mixture of FFAs and CHOL. In vitro permeation studies were performed using ethyl-p-aminobenzoic acid (E-PABA) as a model drug. The flux of E-PABA across the SCS containing the mixture of FFAs was higher than that across the SCS containing a single FA with a chain length of 24 C atoms (FA C24), while the E-PABA flux was not effected by the CER composition. To select the underlying factors for the changes in permeability, the SCSs were examined by Fourier transform infrared spectroscopy (FTIR) and Small angle X-ray scattering (SAXS). All lipid models demonstrated a similar phase behavior. However, when focusing on the conformational ordering of the individual FFA chains, the shorter chain FFA (with a chain length of 16, 18 or 20 C atoms forming only 11m/m% of the total FFA level) had a higher conformational disordering, while the conformational ordering of the chains of the CER and FA C24 and FA C22 hardly did not change irrespective of the composition of the SCS. In conclusion, the conformational mobility of the short chain FFAs present only at low levels in the model SC lipid membranes has a great impact on the permeability of E-PABA.
角质层(SC)中的脂质基质在皮肤屏障功能中起着重要作用。该脂质基质中的主要脂质类别为神经酰胺(CERs)、胆固醇(CHOL)和游离脂肪酸(FFAs)。本研究的目的是确定CER亚类组成和FFAs链长分布的变化是否会影响该基质的通透性。为了对此进行研究,我们使用了脂质模型膜,即角质层替代物(SCS)。我们制备了含有以下成分的SCS:i)单一CER亚类与单一FFA或FFAs和CHOL的混合物;或ii)各种CER亚类的混合物与单一FFA或FFAs和CHOL的混合物。使用对氨基苯甲酸乙酯(E-PABA)作为模型药物进行体外渗透研究。E-PABA穿过含有FFAs混合物的SCS的通量高于穿过含有链长为24个碳原子的单一脂肪酸(FA C24)的SCS的通量,而E-PABA通量不受CER组成的影响。为了选择通透性变化的潜在因素,通过傅里叶变换红外光谱(FTIR)和小角X射线散射(SAXS)对SCS进行了检查。所有脂质模型都表现出相似的相行为。然而,当关注单个FFA链的构象有序性时,较短链的FFA(链长为16、18或20个碳原子,仅占总FFA水平的11m/m%)具有较高的构象无序性,而无论SCS的组成如何,CER和FA C24以及FA C22链的构象有序性几乎没有变化。总之,模型SC脂质膜中仅以低水平存在的短链FFAs的构象流动性对E-PABA的通透性有很大影响。