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PAMAM 树状聚合物与 DOPC 脂质多层膜的相互作用:膜变薄和结构无序。

Interactions between PAMAM dendrimers and DOPC lipid multilayers: Membrane thinning and structural disorder.

机构信息

Bristol Centre for Functional Nanomaterials, H. H. 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.

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

出版信息

Biochim Biophys Acta Gen Subj. 2021 Apr;1865(4):129542. doi: 10.1016/j.bbagen.2020.129542. Epub 2020 Jan 24.

Abstract

BACKGROUND

Understanding the structure of hybrid nanoparticle-lipid multilayers is of fundamental importance to their bioanalytical applications and nanotoxicity, where nanoparticle-membrane interactions play an important role. Poly(amidoamine) (PAMAM) dendrimers are branched polymeric nanoparticles with potential biomedical applications due to precise tunability of their physicochemical properties. Here, the effect of PAMAM dendrimers (2.9-4.5 nm) with either a hydrophilic amine (NH) or a hydrophobic C chain surface termination on the 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC) multilayers has been studied for the first time.

METHODS

DOPC multilayers were created by the liposome-rupture method via drop-casting dendrimer-liposome dispersions with the dendrimers added at different concentrations and at three different stages. The multilayer structure was evaluated via the analysis of the synchrotron X-ray reflectivity (XRR) curves, obtaining the bilayer d-spacing, the coherence length from the Scherrer (L) analysis of the Bragg peaks, and the paracrystalline disorder parameter (g).

RESULTS

Dendrimer addition led to lipid bilayer thinning and more disordered multilayer structures. Larger hydrophobic dendrimers caused greater structural disruption to the multilayers compared to the smaller dendrimers. The smallest, positively charged dendrimers at their highest concentration caused the most pronounced bilayer thinning. The dendrimer-liposome mixing method also affected the multilayer structure due to different dendrimer aggregation involved.

CONCLUSIONS

These results show the complexity of the effect of dendrimer physicochemical properties and the addition method of dendrimers on the structure of mixed dendrimer-DOPC multilayers.

GENERAL SIGNIFICANCE

These insights are useful for fundamental understanding of nanotoxicity and future biomedical application of nanocomposite multilayer materials in which nanoparticles are added for enhanced properties and functionality.

摘要

背景

理解杂交纳米粒子-脂质多层结构对于它们的生物分析应用和纳米毒性至关重要,其中纳米粒子-膜相互作用起着重要作用。聚(酰胺-胺)(PAMAM)树突状聚合物纳米粒子由于其物理化学性质的精确可调性,具有潜在的生物医学应用。在这里,首次研究了具有亲水性胺(NH)或疏水性 C 链表面末端的 PAMAM 树突状聚合物(2.9-4.5nm)对 1,2-二油酰基-sn-甘油-3-磷酸胆碱(DOPC)多层的影响。

方法

通过脂质体破裂法通过滴铸树突状聚合物-脂质体分散体来创建 DOPC 多层,其中树突状聚合物以不同浓度和三个不同阶段添加。通过同步辐射 X 射线反射率(XRR)曲线分析评估多层结构,获得双层 d 间距、布拉格峰的谢勒(L)分析得到的相干长度以及准晶无序参数(g)。

结果

树突状聚合物的添加导致脂质双层变薄和多层结构更加无序。与较小的树突状聚合物相比,较大的疏水性树突状聚合物对多层结构的破坏更大。浓度最高的最小、带正电荷的树突状聚合物导致最明显的双层变薄。由于涉及不同的树突状聚合物聚集,树突状聚合物-脂质体混合方法也会影响多层结构。

结论

这些结果表明,树突状聚合物的物理化学性质和添加方法对混合树突状聚合物-DOPC 多层结构的影响非常复杂。

一般意义

这些见解对于理解纳米毒性以及为了增强性能和功能而添加纳米粒子的纳米复合材料多层材料的未来生物医学应用具有重要意义。

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