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重新审视 β-酪蛋白作为脂质液晶纳米结构颗粒的稳定剂。

Revisiting β-casein as a stabilizer for lipid liquid crystalline nanostructured particles.

机构信息

Department of Biochemistry and Molecular Biology, Monash University, Clayton, Victoria 3800, Australia.

出版信息

Langmuir. 2011 Dec 20;27(24):14757-66. doi: 10.1021/la203061f. Epub 2011 Nov 18.

Abstract

Lipid liquid crystalline nanoparticles such as cubosomes and hexosomes have unique internal nanostructures that have shown great potential in drug and nutrient delivery applications. The triblock copolymer, Pluronic F127, is usually employed as a steric stabilizer in dispersions of lipid nanostructured particles. In this study, we investigated the formation, colloidal stability and internal nanostructure and morphology of glyceryl monooleate (GMO) and phytantriol (PHYT) cubosome dispersions on substituting β-casein with F127 in increasing proportion as the stabilizer. Internal structure and particle morphology were evaluated using small-angle X-ray scattering (SAXS) and cryo-transmission electron microscopy (cryo-TEM), while protein secondary structure was studied using synchrotron radiation circular dichroism (SRCD). The GMO cubosome dispersion stabilized by β-casein alone displayed a V(2) (Pn3m) phase structure and a V(2) to H(2) phase transition at 60 °C. In comparison, F127-stabilized GMO dispersion had a V(2) (Im3m) phase structure and the H(2) phase only appeared at higher temperature, that is, 70 °C. In the case of PHYT dispersions, only the V(2) (Pn3m) phase structure was observed irrespective of the type and concentration of stabilizers. However, β-casein-stabilized PHYT dispersion displayed a V(2) to H(2) to L(2) transition behavior upon heating, whereas F127-stabilized PHYT dispersion displayed only a direct V(2) to L(2) transition. The protein secondary structure was not disturbed by interaction with GMO or PHYT cubosomes. The results demonstrate that β-casein provides steric stabilization to dispersions of lipid nanostructured particles and avoids the transition to Im3m structure in GMO cubosomes, but also favors the formation of the H(2) phase, which has implications in drug formulation and delivery applications.

摘要

脂质液晶纳米粒子,如立方纳米囊和六方纳米囊,具有独特的内部纳米结构,在药物和营养物质传递应用中显示出巨大的潜力。三嵌段共聚物 Pluronic F127 通常用作脂质纳米结构粒子分散体的空间位阻稳定剂。在这项研究中,我们研究了在取代β-酪蛋白时,甘油单油酸酯(GMO)和植物三醇(PHYT)立方纳米囊分散体的形成、胶体稳定性以及内部纳米结构和形态,使用 F127 作为稳定剂的比例逐渐增加。使用小角 X 射线散射(SAXS)和冷冻传输电子显微镜(cryo-TEM)评估内部结构和颗粒形态,同时使用同步辐射圆二色性(SRCD)研究蛋白质二级结构。单独用β-酪蛋白稳定的 GMO 立方纳米囊分散体显示出 V(2)(Pn3m)相结构,在 60°C 时发生 V(2)到 H(2)的相转变。相比之下,F127 稳定的 GMO 分散体具有 V(2)(Im3m)相结构,并且仅在更高温度下即 70°C 时才出现 H(2)相。对于 PHYT 分散体,无论稳定剂的类型和浓度如何,仅观察到 V(2)(Pn3m)相结构。然而,β-酪蛋白稳定的 PHYT 分散体在加热时显示出 V(2)到 H(2)到 L(2)的转变行为,而 F127 稳定的 PHYT 分散体仅显示出直接的 V(2)到 L(2)的转变。蛋白质二级结构未受到与 GMO 或 PHYT 立方纳米囊相互作用的干扰。结果表明,β-酪蛋白为脂质纳米结构粒子的分散体提供了空间位阻稳定性,并避免了 GMO 立方纳米囊向 Im3m 结构的转变,但也有利于 H(2)相的形成,这对药物制剂和传递应用具有重要意义。

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