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Liposome structure imaging by atomic force microscopy: Verification of improved liposome stability during adsorption of multiple aggregated vesicles

机译:通过原子力显微镜对脂质体结构成像:验证多个聚集的囊泡吸附过程中改善的脂质体稳定性

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Atomic force microscopy has enabled direct visualization of the liposome structure supported on mica surfaces in air and silanized mica surfaces in aqueous media. The images display distinct patterns of adhered liposomes: multiple and single vesicle liposomes and flat supported bilayers. The multiple vesicle liposome structure is not visible by optical microscopy since the vesicles forming the liposome have diameters as small as 20 rim. Molecularly resolved force versus distance curves displaying the organization of hydrocarbon chains (mono- or bilayers) corroborate the presence of distinct adsorbed structures observed by scanning the surface. The high resolution of the observed liposome images allows the visualization of the aggregation of the multiple vesicles forming liposomes which were shown to have their origin in the liposome formation process and not during adsorption. Since most of the observed liposomes are aggregated vesicles, this aggregated structure has a substantially larger stability during adsorption than the single vesicle structure and consequently a larger resistance in maintaining its shape and function as a carrier of cosmetics, food additives, and drugs. This observation also has some important consequences in the liposomes' selective permeability when they are used as carriers. [References: 22]
机译:原子力显微镜可以直接观察空气中云母表面和水性介质中硅烷化云母表面所支持的脂质体结构。图像显示了粘附的脂质体的不同模式:多个和单个囊泡脂质体以及平坦支撑的双层。由于形成脂质体的囊泡的直径小至20个边缘,因此通过光学显微镜看不到多囊泡脂质体的结构。分子分辨力与距离的关系曲线显示了烃链(单层或双层)的组织,证实了通过扫描表面观察到的独特吸附结构的存在。观察到的脂质体图像的高分辨率允许可视化形成脂质体的多个囊泡的聚集,这些脂质体显示其起源于脂质体形成过程而不是在吸附过程中。由于观察到的大多数脂质体是聚集的囊泡,因此该聚集的结构在吸附过程中的稳定性要比单个囊泡的结构大得多,因此在保持其形状和用作化妆品,食品添加剂和药物的载体方面具有更大的抵抗力。当将脂质体用作载体时,该观察结果也对脂质体的选择性渗透性具有重要意义。 [参考:22]

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