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Lipogels for Encapsulation of Hydrophilic Proteins and Hydrophobic Small Molecules

机译:用于亲水蛋白和疏水性小分子包封的脂质体

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摘要

Lipid-polymer hybrid materials have the potential to exhibit enhanced stability and loading capabilities in comparison to parent liposome or polymer materials. However, complexities lie in formulating and characterizing such complex nanomaterials. Here we describe a lipid-coated polymer gel (lipogel) formulated using a single pot methodology, where self-assembling liposomes template a UV-curable polymer gel core. Using fluorescently-labeled lipids, protein, and hydrophobic molecules, we have characterized their formation, purification, stability, and encapsulation efficiency via common instrumentation methods such as dynamic light scattering (DLS), matrix-assisted laser desorption ionization-mass spectrometry (MALDI-MS), UV-Vis spectroscopy, fluorescence spectroscopy, and single particle total internal reflection fluorescence (TIRF) microscopy. In addition, we confirmed that these dual-guest loaded lipogels are stable in solution for several months. The simplicity of this complete aqueous formation and non-covalent dual-guest encapsulation holds potential as a tunable nanomaterial scaffold.
机译:与母体脂质体或聚合物材料相比,脂质-聚合物杂化材料具有表现出增强的稳定性和负载能力的潜力。然而,复杂性在于配制和表征这种复杂的纳米材料。在这里,我们描述了使用单罐方法配制的脂质包覆的聚合物凝胶(lipogel),其中自组装脂质体以可紫外线固化的聚合物凝胶核心为模板。我们使用荧光标记的脂质,蛋白质和疏水分子,通过常见的仪器方法,例如动态光散射(DLS),基质辅助激光解吸电离质谱(MALDI-),对它们的形成,纯化,稳定性和包封效率进行了表征。 MS),UV-Vis光谱,荧光光谱和单粒子全内反射荧光(TIRF)显微镜。另外,我们证实了这些负载双客体的脂凝胶在溶液中稳定数月。这种完全的水形成和非共价双客人封装的简单性具有作为可调纳米材料支架的潜力。

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