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The effect of membrane softeners on rigidity of lipid vesicle bilayers: Derivation from vesicle size changes

机译:膜柔软剂对脂质囊泡双层刚性的影响:囊泡尺寸变化的衍生

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Deformability is not just a fundamentally interesting vesicle characteristic; it is also the key determinant of vesicle ability to cross the skin barrier; i.e. skin penetrability. Development of bilayer vesicles for drug and vaccine delivery across the skin should hence involve optimization of this property, which is controllable by the concentration of bilayer softeners in or near the vesicle bilayers. To this end, we propose a simple method for quantifying the effect of bilayer softeners on deformability of bilayer vesicles. The method derives the bending rigidity of vesicle bilayers from vesicle size dependence on softener concentration. To exemplify the method, we studied mixtures of soybean phosphatidylcholine with anionic sodium deoxycholate, non-ionic polyoxyethylene (20) sorbitan oleyl ester (polysorbate 80), or non-ionic polyoxyethylene (20) oleyl ether (C18:1EO20, Brij 98). With each of the tested bilayer softeners, the bending rigidity of the resulting mixed-amphipat vesicle bilayers decreased quasi-exponentially as the concentration of the bilayer softener increased, as one would expect on theoretical ground. The bilayer bending rigidity reached low values, near the thermal stability limit, i.e. k(B)T, before vesicle transformation into non-vesicular aggregates began. For a soybean phosphatidylcholine concentration of 5.0 mmol kg(-1), the bilayer bending rigidity reached 1.5 kBT at the total deoxycholate concentration of 4.1 mmol kg(-1) and 3.4 kBT at the total polysorbate 80 concentration of 2.0 mmol kg(-1). In the case of C18:1EO20 the bilayer bending rigidity reached 1.5 kBT at the bilayer surface occupancy alpha = 0.1. The dependence of vesicle size on bilayer softener concentration thus reveals vesicle transformation into different aggregate structures (such as mixed micelles with poor skin penetrability) and practically valuable information on vesicle deformability. Our results compare favorably with results of literature measurements. We provide p
机译:可变形性不仅仅是一个基本上有趣的囊泡特征;它也是囊泡穿过皮肤屏障的关键决定因素;即皮肤渗透性。在皮肤上的药物和疫苗递送的双层囊泡的研制应因此涉及该性能的优化,其可通过囊泡双层的双层柔软剂的浓度控制。为此,我们提出了一种简单的方法,用于量化双层柔软剂对双层囊泡的可变形性的影响。该方法产生囊泡双层的弯曲刚度,从囊泡尺寸依赖于柔软剂浓度。为了举例说明该方法,我们研究了与阴离子脱氧胆酸钠,非离子聚氧乙烯(20)脱水山梨糖醇油酯(聚山梨醇酯80)或非离子聚氧乙烯(20)油醚(C18:1EO20,Brij 98)的混合物。随着每个测试的双层柔软剂,所得的混合--Amphipat囊泡双层的弯曲刚度随着双层柔软剂的浓度增加而导致准指数降低,因为人们对理论磨实的期望。双层弯曲刚度达到低值,靠近热稳定性极限,即K(b)T,在囊泡转化到非囊泡聚集体之前开始。对于5.0mmol kg(-1)的大豆磷脂酰胆碱浓度,双层弯曲刚度在总热山梨醇酯80mmol kg(-1)的总脱氧胆酸盐浓度为4.1mmol kg(-1)和3.4kbt,达到1.5kbt。浓度为2.0mmol kg(-1 )。在C18:1EO20的情况下,双层弯曲刚度在双层表面占用α= 0.1处达到1.5kBt。因此,囊泡尺寸对双层柔软剂浓度的依赖性揭示了囊泡转变成不同的聚集体结构(例如皮肤渗透性差的混合胶束)和实际上有价值的关于囊泡可变形性的信息。我们的结果与文献测量结果有利相比。我们提供P.

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