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首页> 外文期刊>ACS Omega >Liquid Crystalline Nanostructures as PEGylated Reservoirs of Omega-3 Polyunsaturated Fatty Acids: Structural Insights toward Delivery Formulations against Neurodegenerative Disorders
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Liquid Crystalline Nanostructures as PEGylated Reservoirs of Omega-3 Polyunsaturated Fatty Acids: Structural Insights toward Delivery Formulations against Neurodegenerative Disorders

机译:液晶纳米结构作为Omega-3多不饱和脂肪酸的PEG化储库:对神经退行性疾病的传递配方的结构见解。

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Omega-3 polyunsaturated fatty acids (ω-3 PUFAs) are bioactive lipids with considerable impact in medicine and nutrition. These compounds exert structuring effects on the cellular membrane organization, regulate the gene expression, and modulate various signaling cascades and metabolic processes. The purpose of the present work is to demonstrate the structural features of ω-3 PUFA-containing three-dimensional supramolecular lipid assemblies suitable for pharmaceutical applications that require soft porous carriers. We investigate the liquid crystalline structures formed upon mixing of eicosapentaenoic acid (EPA, 20:5) with the lyotropic nonlamellar lipid monoolein and the formation of multicompartment assemblies. Starting with the monoolein-based lipid cubic phase, double membrane vesicles, cubosome precursors, sponge-type particles (spongosomes), mixed intermediate nonlamellar structures, and multicompartment assemblies are obtained through self-assembly at different amphiphilic compositions. The dispersions containing spongosomes as well as nanocarriers with oil and vesicular compartments are stabilized by PEGylation of the lipid/water interfaces using a phospholipid with a poly(ethylene glycol) chain. The microstructures of the bulk mixtures were examined by cross-polarized light optical microscopy. The dispersed liquid crystalline structures and intermediate states were studied by small-angle X-ray scattering, cryogenic transmission electron microscopy, and quasielastic light scattering techniques. They established that PUFA influences the phase type and the sizes of the aqueous compartments of the liquid crystalline carriers. The resulting multicompartment systems and stealth nanosponges may serve as mesoporous reservoirs for coencapsulation of ω-3 PUFA (e.g., EPA) with water-insoluble drugs and hydrophilic macromolecules toward development of combination treatment strategies of neurodegenerative and other diseases.
机译:Omega-3多不饱和脂肪酸(ω-3PUFA)是具有生物活性的脂质,对药物和营养产生重大影响。这些化合物对细胞膜组织发挥结构作用,调节基因表达,并调节各种信号级联和代谢过程。本工作的目的是证明适用于需要软质多孔载体的药物应用的含ω-3PUFA的三维超分子脂质组装体的结构特征。我们研究了二十碳五烯酸(EPA,20:5)与溶致性非片状脂质单油精混合后形成的液晶结构,以及多隔室组件的形成。从基于单油精的脂质立方相开始,通过在不同两亲组合物上进行自组装,可以获得双层膜囊泡,立方体前体,海绵型颗粒(海绵体),混合的中间非层状结构和多隔室组合。通过使用具有聚(乙二醇)链的磷脂使脂质/水界面的PEG化来稳定含有海绵体以及具有油和囊泡区室的纳米载体的分散体。通过交叉偏振光光学显微镜检查本体混合物的微观结构。通过小角X射线散射,低温透射电子显微镜和准弹性光散射技术研究了分散的液晶结构和中间态。他们确定了PUFA会影响液晶载体的相类型和水相隔室的尺寸。所得的多隔室系统和隐形纳米海绵可充当介孔储库,用于将ω-3PUFA(例如EPA)与水不溶性药物和亲水性大分子共包封,以开发神经退行性疾病和其他疾病的联合治疗策略。

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