Model lipid bilayers mimic non-specific interactions of gold nanoparticles with macrophage plasma membranes

被引:36
|
作者
Montis, Costanza [1 ,2 ]
Generini, Viola [1 ,2 ]
Boccalini, Giulia [3 ]
Bergese, Paolo [4 ,5 ]
Bani, Daniele [3 ]
Berti, Debora [1 ,2 ]
机构
[1] Univ Florence, Dept Chem, Via Lastruccia 3, I-50019 Florence, Italy
[2] Univ Florence, CSGI, Via Lastruccia 3, I-50019 Florence, Italy
[3] Univ Florence, Dept Expt & Clin Med, Viale Pieraccini 6, I-50139 Florence, Italy
[4] Univ Brescia, CSGI, Dept Mol & Translat Med, I-25123 Brescia, Italy
[5] Univ Brescia, INSTM, I-25123 Brescia, Italy
关键词
Gold nanoparticles; Gold nanorods; Biomimetic membranes; Supported lipid bilayers; Giant unilamellar vesicles; Nanomedicine; INTERNALIZATION; VESICLES;
D O I
10.1016/j.jcis.2018.01.064
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Understanding the interaction between nanomaterials and biological interfaces is a key unmet goal that still hampers clinical translation of nanomedicine. Here we investigate and compare non-specific interaction of gold nanoparticles (AuNPs) with synthetic lipid and wild type macrophage membranes. A comprehensive data set was generated by systematically varying the structural and physicochemical properties of the AuNPs (size, shape, charge, surface functionalization) and of the synthetic membranes (composition, fluidity, bending properties and surface charge), which allowed to unveil the matching conditions for the interaction of the AuNPs with macrophage plasma membranes in vitro. This effort directly proved for the first time that synthetic bilayers can be set to mimic and predict with high fidelity key aspects of nanoparticle interaction with macrophage eukaryotic plasma membranes. It then allowed to model the experimental observations according to classical interface thermodynamics and in turn determine the paramount role played by non-specific contributions, primarily electrostatic, Van der Waals and bending energy, in driving nanoparticle-plasma membrane interactions. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:284 / 294
页数:11
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