| Autor: |
Ceri J. Richards, Majid Ahmadi, Marc C. A. Stuart, Bart J. Kooi, Christoffer Åberg, Wouter H. Roos |
| Přispěvatelé: |
Pharmaceutical Analysis, Nanostructured Materials and Interfaces, Electron Microscopy, Stratingh Institute of Chemistry, Medicinal Chemistry and Bioanalysis (MCB), Molecular Biophysics |
| Jazyk: |
angličtina |
| Rok vydání: |
2023 |
| Předmět: |
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| Zdroj: |
Nanoscale, 15(1), 248-258. ROYAL SOC CHEMISTRY |
| ISSN: |
2040-3364 |
| Popis: |
The current lack of insight into nanoparticle-cell membrane interactions hampers smart design strategies and thereby the development of effective nanodrugs. Quantitative and methodical approaches utilizing cell membrane models offer an opportunity to unravel particle-membrane interactions in a detailed manner under well controlled conditions. Here we use total internal reflection microscopy for real-time studies of the non-specific interactions between nanoparticles and a model cell membrane at 50 ms temporal resolution over a time course of several minutes. Maintaining a simple lipid bilayer system across conditions, adsorption and desorption were quantified as a function of biomolecular corona, particle size and fluid flow. The presence of a biomolecular corona reduced both the particle adsorption rate onto the membrane and the duration of adhesion, compared to pristine particle conditions. Particle size, on the other hand, was only observed to affect the adsorption rate. The introduction of flow reduced the number of adsorption events, but increased the residence time. Lastly, altering the composition of the membrane itself resulted in a decreased number of adsorption events onto negatively charged bilayers compared to neutral bilayers. Overall, a model membrane system offers a facile platform for real-time imaging of individual adsorption-desorption processes, revealing complex adsorption kinetics, governed by particle surface energy, size dependent interaction forces, flow and membrane composition. |
| Databáze: |
OpenAIRE |
| Externí odkaz: |
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