Engineered silica nanoparticles interact differently with lipid monolayers compared to lipid bilayers
Autor: | Saeed Nazemidashtarjandi, Allan E. David, Ali Asghari Adib, Adelaide Kruse, Amir M. Farnoud, Alexander Kelly, Katherine Cimatu |
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Rok vydání: | 2018 |
Předmět: |
Chemistry
Materials Science (miscellaneous) Vesicle Nanoparticle 02 engineering and technology 010402 general chemistry 021001 nanoscience & nanotechnology 01 natural sciences 0104 chemical sciences Cell membrane chemistry.chemical_compound Membrane medicine.anatomical_structure PEG ratio Monolayer medicine Biophysics 0210 nano-technology Lipid bilayer Ethylene glycol General Environmental Science |
Zdroj: | Environmental Science: Nano. 5:289-303 |
ISSN: | 2051-8161 2051-8153 |
DOI: | 10.1039/c7en00685c |
Popis: | Despite a number of fundamental studies, the interactions of engineered nanoparticles with the cell plasma membrane are still not well understood. Membrane models, such as lipid monolayers and bilayers, have been used to provide a mechanistic understanding of nanoparticle effects on the structure and integrity of the cell membrane. However, the role of the membrane model itself in regulating nanoparticle–lipid interactions has generally been overlooked. In an effort to elucidate how changing the membrane model affects the resulting interactions with nanoparticles, the current study investigates the interaction of silica nanoparticles (104 ± 5 nm) with different surface-functional groups: plain (silanol), amine, and poly(ethylene glycol) (PEG), with various molecular weights of 2k, 5k, and 20k Daltons, with lipid monolayers and bilayers of the same composition. Studies with lipid monolayers demonstrated that PEGylated particles, regardless of the PEG molecular weight, and unlike plain and amine-modified particles, were able to penetrate the monolayer and disrupt the structure of lipids as evidenced by tensiometry and atomic force microscopy. In contrast, when interacting with lipid bilayers in suspension (i.e. vesicles), plain, amine-modified, and PEG 20k-modified particles disrupted vesicle structure, causing significant leakage, while PEG 2k- and 5k-modified particles did not affect the integrity of the vesicles. In summary, while the interactions of silica nanoparticles with membrane models is dependent on particle surface properties, a clear difference is observed in particle interactions with lipid monolayers compared to bilayers. |
Databáze: | OpenAIRE |
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