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由于树枝状聚合物纳米粒子的插入,脂质中间相的结构变化:肿胀的层状结构、曲率降低和结构无序度增加。

Structural changes in lipid mesophases due to intercalation of dendritic polymer nanoparticles: Swollen lamellae, suppressed curvature, and augmented structural disorder.

机构信息

School of Chemistry, University of Bristol, Cantock's Close, Bristol, BS8 1TS, UK; Bristol Centre for Functional Nanomaterials, HH Wills Physics Laboratory, University of Bristol, Tyndall Avenue, Bristol, BS8 1TL, UK.

School of Chemistry, University of Bristol, Cantock's Close, Bristol, BS8 1TS, UK.

出版信息

Acta Biomater. 2020 Mar 1;104:198-209. doi: 10.1016/j.actbio.2019.12.036. Epub 2020 Jan 3.

Abstract

Understanding interactions between nanoparticles and model membranes is relevant to functional nano-composites and the fundamentals of nanotoxicity. In this study, the effect of polyamidoamine (PAMAM) dendrimers as model nanoparticles (NP) on the mesophase behaviour of 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphoethanolamine (POPE) has been investigated using high-pressure small-angle X-ray scattering (HP-SAXS). The pressure-temperature (p-T) diagrams for POPE mesophases in excess water were obtained in the absence and presence of G2 and G4 polyamidoamine (PAMAM) dendrimers (29 Å and 45 Å in diameter, respectively) at varying NP-lipid number ratio (ν = 0.0002-0.02) over the pressure range p = 1-3000 bar and temperature range T = 20-80 °C. The p-T phase diagram of POPE exhibited the L, L and H phases. Complete analysis of the phase diagrams, including the relative area pervaded by different phases, phase transition temperatures (T) and pressures (p), the lattice parameters (d-spacing), the pressure-dependence of d-spacing (Δd/Δp), and the structural ordering in the mesophase as gauged by the Scherrer coherence length (L) permitted insights into the size- and concentration-dependent interactions between the dendrimers and the model membrane system. The addition of dendrimers changed the phase transition pressure and temperature and resulted in the emergence of highly swollen lamellar phases, dubbed L and L. G4 PAMAM dendrimers at the highest concentration ν = 0.02 suppressed the formation of the H phase within the temperature range studied, whereas the addition of G2 PAMAM dendrimers at the same concentration promoted an extended mixed lamellar region in which L and L phases coexisted. STATEMENT OF SIGNIFICANCE: Using high pressure small angle X-ray scattering in the pressure range 1-3000 bar and temperature range 20-60 °C, we have studied interactions between PAMAM dendrimers (as model nanoparticles) and POPE lipid mesophases (as model membranes). We report the pressure-temperature phase diagrams for the dendrimer-lipid mesophases for the first time. We find that the dendrimers alter the phase transition temperatures (T) and pressures (p), the lattice parameters (d-spacing), and the structural order in the mesophase. We interpret these unprecedented results in terms of the fluidity of the lipid membranes and the interactions between the dendrimers and the membranes. Our findings are of fundamental relevance to the field of nanotoxicity and functional nanomaterials that integrate nanoparticles and organized lipid structures.

摘要

了解纳米颗粒与模型膜之间的相互作用对于功能性纳米复合材料和纳米毒性的基本原理至关重要。在这项研究中,使用高压小角 X 射线散射 (HP-SAXS) 研究了聚酰胺胺 (PAMAM) 树状大分子作为模型纳米颗粒 (NP) 对 1-棕榈酰基-2-油酰基-sn-甘油-3-磷酸乙醇胺 (POPE) 中间相行为的影响。在 20-80°C 的温度范围内和 1-3000 巴的压力范围内,获得了在过量水中 POPE 中间相的压力-温度 (p-T) 图,在不同的 NP-脂质比 (ν=0.0002-0.02) 下,没有和存在 G2 和 G4 聚酰胺胺 (PAMAM) 树状大分子 (直径分别为 29 Å 和 45 Å)。POPE 的 p-T 相图显示了 L、L 和 H 相。通过相对不同相所占的面积、相转变温度 (T) 和压力 (p)、晶格参数 (d 间距)、d 间距随压力的变化 (Δd/Δp) 以及中间相的结构有序性(由谢勒相干长度 (L) 来衡量),对相图进行了全面分析,这些分析使我们能够深入了解树状大分子与模型膜系统之间的尺寸和浓度依赖性相互作用。树状大分子的添加改变了相转变压力和温度,并导致高度溶胀的层状相的出现,称为 L 和 L。在研究的温度范围内,最高浓度 ν=0.02 的 G4 PAMAM 树状大分子抑制了 H 相的形成,而相同浓度的 G2 PAMAM 树状大分子的添加促进了 L 和 L 相共存的扩展混合层状区域。意义声明:使用高压小角 X 射线散射在 1-3000 巴的压力范围和 20-60°C 的温度范围内,我们研究了 PAMAM 树状大分子 (作为模型纳米颗粒) 和 POPE 脂质中间相 (作为模型膜) 之间的相互作用。我们首次报告了树状大分子-脂质中间相的压力-温度相图。我们发现树状大分子改变了相转变温度 (T) 和压力 (p)、晶格参数 (d 间距) 和中间相的结构有序性。我们根据脂质膜的流动性和树状大分子与膜之间的相互作用来解释这些前所未有的结果。我们的发现对于纳米毒性和整合纳米颗粒和组织化脂质结构的功能性纳米材料领域具有根本意义。

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