Tear of lipid membranes by nanoparticles (original) (raw)
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Interaction of nanoparticles with lipid membranes: a multiscale perspective
Nanoscale, 2014
A nanoscale range of surface feature curvatures where lipid membranes lose integrity and form pores has been found experimentally. The pores were experimentally observed in the L-r-dimyristoyl phosphatidylcholine membrane around 1.2-22 nm polar nanoparticles deposited on mica surface. Lipid bilayer envelops or closely follows surface features with the curvatures outside of that region. This finding provides essential information for the understanding of nanoparticle-lipid membrane interaction, cytotoxicity, preparation of biomolecular templates and supported lipid membranes on rough and patterned surfaces.
Wide Varieties of Cationic Nanoparticles Induce Defects In Supported Lipid Bilayers
Nano Lett, 2008
Nanoparticles with widely varying physical properties and origins (spherical versus irregular, synthetic versus biological, organic versus inorganic, flexible versus rigid, small versus large) have been previously noted to translocate across the cell plasma membrane. We have employed atomic force microscopy to determine if the physical disruption of lipid membranes, formation of holes and/or thinned regions, is a common mechanism of interaction between these nanoparticles and lipids. It was found that a wide variety of nanoparticles, including a cell penetrating pepide (MSI-78), a protein (TAT), polycationic polymers (PAMAM dendrimers, pentanol-core PAMAM dendrons, polyethyleneimine, and diethylaminoethyl-dextran), and two inorganic particles (Au-NH 2, SiO 2-NH 2), can induce disruption, including the formation of holes, membrane thinning, and/or membrane erosion, in supported lipid bilayers.
Effects of nanobubble collapse on cell membrane integrity
Journal of Micromechanics and Molecular Physics, 2017
Recent studies have shown that ultrasound is used to open drug-carrying liposomes to release their payloads; however, a shockwave energetic enough to rupture lipid membranes can cause collateral damage to surrounding cells. Similarly, a destructive shockwave, which may be used to rupture a cell membrane in order to lyse the cell (e.g., as in cancer treatments) may also impair or destroy nearby healthy tissue. To address this problem, we use dissipative particle dynamic (DPD) simulation to investigate the addition of a cavitation bubble between the shockwave and the model cell membrane to alter the shockwave front, allowing low-velocity shockwaves to specifically damage an intended target. We focus specifically on a spherical lipid bilayer model, and note the effect of shockwave velocity, bubble size, and orientation on the damage to the model cell. We show that a cavitation bubble greatly decreases the necessary shockwave velocity required to damage the lipid bilayer and rupture the...
Cationic Nanoparticles Induce Nanoscale Disruption in Living Cell Plasma Membranes
The Journal of Physical Chemistry B, 2009
It has long been recognized that cationic nanoparticles induce cell membrane permeability. Recently, it has been found that cationic nanoparticles induce the formation and/or growth of nanoscale holes in supported lipid bilayers. In this paper, we show that noncytotoxic concentrations of cationic nanoparticles induce 30-2000 pA currents in 293A (human embryonic kidney) and KB (human epidermoid carcinoma) cells, consistent with a nanoscale defect such as a single hole or group of holes in the cell membrane ranging from 1 to 350 nm 2 in total area. Other forms of nanoscale defects, including the nanoparticle porating agents adsorbing onto or intercalating into the lipid bilayer, are also consistent; although the size of the defect must increase to account for any reduction in ion conduction, as compared to a water channel. An individual defect forming event takes 1-100 ms, while membrane resealing may occur over tens of seconds. Patch-clamp data provide direct evidence for the formation of nanoscale defects in living cell membranes. The cationic polymer data are compared and contrasted with patch-clamp data obtained for an amphiphilic phenylene ethynylene antimicrobial oligomer (AMO-3), a small molecule that is proposed to make well-defined 3.4 nm holes in lipid bilayers. Here, we observe data that are consistent with AMO-3 making ∼3 nm holes in living cell membranes.
International Journal of Biomedical Nanoscience and Nanotechnology, 2013
Engineered nanomaterials (ENMs) have attractive functional properties and are increasingly being used in commercial products. However, ENMs present health risks that are poorly understood and difficult to assess. Because ENMs must interface with cell membranes to cause biological effects, improved methods are needed to measure ENM-biomembrane interactions. The goals of this paper are to review the current status of methods to characterise interactions between ENMs and bilayer lipid membranes that mimic cell membranes, and to present example applications of the methods relevant to nanotoxicology. Four approaches are discussed: electrochemical methods that measure ENM-induced ion leakage through lipid bilayers, optical methods that measure dye leakage from liposomes, partitioning methods that measure ENM distribution coefficients between aqueous solution and immobilised lipid bilayers, and theoretical models capable of predicting fundamental molecular interactions between ENMs and biomembranes. For each approach, current literature is summarised, recent results are given, and future prospects are analysed, including the potential to be used in a high-throughput mode. The relative advantages of the various approaches are discussed, along with their synergistic potential to provide multi-dimensional characterisation of ENM-biomembrane interactions for robust health risk assessment algorithms. ) 'Engineered nanomaterial interactions with bilayer lipid membranes: screening platforms to assess nanoparticle toxicity', Int.
Nanoparticle Interaction with Biological Membranes: Does Nanotechnology Present a Janus Face?
Accounts of Chemical Research, 2007
Polycationic organic nanoparticles are shown to disrupt model biological membranes and living cell membranes at nanomolar concentrations. The degree of disruption is shown to be related to nanoparticle size and charge as well as to the phase, fluid liquid crystalline or gel, of the biological membrane. Disruption events on model membranes have been directly imaged using scanning probe microsopy whereas disruption events on living cells have been analyzed using cytosolic enzyme leakage assays, dye diffusion assays, and fluorescence microscopy.
Lipid artificial tears at a mimetic ocular interface
Chemistry and Physics of Lipids, 2021
We studied the behaviour of three lipid tear products, commercialised by the same brand, as Langmuir films at the air/liquid interface to simulate the ocular environment. No significant differences were observed in the surface behaviour of two of them disclosing the same composition, but commercialised for different applications. The interaction of several subphases, namely sodium chloride, glucose, albumin and lysozyme present in the natural tear, with the lipid films was assessed at room temperature and the temperature of human tear using surface pressure-area isotherms and elastic modulus plots. There is a notable influence of sodium chloride and the proteins albumin and lysozyme on the surface pressure-area isotherm of the lipid Langmuir films. Albumin shifted this isotherm to lower areas while an opposite shift was caused by lysozyme. These studies could be useful for the formulation of new lipid-containing artificial tears, and for increasing the confidence of the customers in commercial eye care formulations.
Surface Charge Dependent Nanoparticle Disruption and Deposition of Lipid Bilayer Assemblies
Langmuir, 2012
Electrostatic interaction plays a leading role in nanoparticle interactions with membrane architectures and can lead to effects such as nanoparticle binding and membrane disruption. In this work, the effects of nanoparticles (NPs) interacting with mixed lipid systems were investigated, indicating an ability to tune both NP binding to membranes and membrane disruption. Lipid membrane assemblies (LBAs) were created using a combination of charged, neutral, and gel-phase lipids. Depending on the lipid composition, nanostructured networks could be observed using in situ atomic force microscopy representing an asymmetrical distribution of lipids that rendered varying effects on NP interaction and membrane disruption that were domainspecific. LBA charge could be localized to fluidic domains that were selectively disrupted when interacting with negatively charged Au nanoparticles or quantum dots. Disruption was observed to be related to the charge density of the membrane, with a maximum amount of disruption occurring at ∼40% positively charged lipid membrane concentration. Conversely, particle deposition was determined to begin at charged lipid concentrations greater than 40% and increased with charge density. The results demonstrate that the modulation of NP and membrane charge distribution can play a pivitol role in determining NPinduced membrane disruption and NP surface assembly.