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工程化两亲性烯基脂质用于功能混合纳米结构中的自组装。

Engineering amphiphilic alkenyl lipids for self-assembly in functional hybrid nanostructures.

机构信息

Departamento de Química Orgánica y Farmacéutica, Facultad de Farmacia, Universidad de Sevilla, c/ Profesor García González, 2, Sevilla, 41012, Spain.

Biomedical Magnetic Resonance Laboratory-BMRL, Andalusian Public Foundation Progress and Health-FPS, Seville, Spain.

出版信息

Sci Rep. 2024 Nov 21;14(1):28887. doi: 10.1038/s41598-024-79917-8.

Abstract

The development of biocompatible hybrid nanosystems for advanced functional applications presents significant challenges to the research community. Key obstacles include the poor solubility of these nanosystems in water and the difficulty of precisely controlling their nanostructure dimensions and composition. A promising approach to overcoming these challenges is the self-assembly of surfactant-based building blocks into well-ordered hybrid nanostructures. In this study, we explore the relationship between structure and self-assembly in novel low molecular weight amphiphilic molecules to produce stable and biocompatible hybrid nanostructures. We investigated the self-assembly behavior of two families of amphiphiles derived from alkenyl lipids with one or two double bonds, leading to distinct hybrid supramolecular structures facilitated by the incorporation of hydrophobic iron oxide nanoparticles (IONPs) as templates. The presence of double bonds in the lipid tail and the morphology of the amphiphile influence the arrangement on the hydrophobic NPs. Amphiphiles with a single double bond in the lipid tail form highly water-soluble, well-ordered micellar-like structures on the IONP surfaces, while those with two double bonds create disordered lipid nanoparticles. Furthermore, these amphiphilic molecules can self-organize into higher-order hybrid supramolecular structures, such as vesicles, with potential applications in magnetic resonance imaging (MRI).

摘要

用于高级功能应用的生物相容性混合纳米系统的开发给研究界带来了重大挑战。关键障碍包括这些纳米系统在水中的溶解度差,以及精确控制其纳米结构尺寸和组成的困难。克服这些挑战的一种有前途的方法是将基于表面活性剂的构建块自组装成有序的混合纳米结构。在这项研究中,我们探索了新型低分子量两亲分子的结构与自组装之间的关系,以产生稳定和生物相容的混合纳米结构。我们研究了两种源于具有一个或两个双键的烯基脂质的两亲分子的自组装行为,导致通过掺入疏水性氧化铁纳米颗粒(IONP)作为模板来促进混合超分子结构。脂质尾部的双键存在和两亲分子的形态影响疏水 NP 上的排列。在脂质尾部具有单个双键的两亲分子在 IONP 表面上形成高度水溶性、有序的胶束样结构,而具有两个双键的两亲分子则形成无序的脂质纳米颗粒。此外,这些两亲分子可以自组织成更高阶的混合超分子结构,例如囊泡,在磁共振成像(MRI)中有潜在的应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afac/11582357/c3ea58758ed6/41598_2024_79917_Fig1_HTML.jpg

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