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Cellular uptake and retention of nanoparticles: Insights on particle properties and interaction with cellular components

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submitted on 2023-10-05, 09:16 and posted on 2023-10-05, 11:34 authored by Robin Augustine, Anwarul Hasan, Rosita Primavera, Rudilyn Joyce Wilson, Avnesh S. Thakor, Bhavesh D. Kevadiya

The utilization of nanomaterials in the biological and medical field is quickly progressing, particularly in areas where traditional diagnostics and treatment approaches have limited success. The success of nanomaterials in medical products such as biomedical implants, wound dressings and drug delivery systems rely upon their effective interaction between the extracellular matrix, cells, and intracellular components. Upon contact with mammalian cells, nanoparticles (NPs) begin to interact with the extracellular matrix, cell membrane, cytoplasmic proteins, nucleus, and other cellular organelles, which result in nanoparticle internalization and subsequent cellular responses. Such responses elicited by the mammalian cells as a result of the cell-nanomaterials interactions, both at the cellular and molecular level, are mainly determined by the morphological, chemical, and surface characteristics of the nanomaterials themselves. This review provides an overview of how such different attributes, such as chemical nature, size, shape, surface charge, topography, stiffness, and functional features of nanomaterials, influence the cell-nanomaterials interactions.

Other Information

Published in: Materials Today Communications
License: http://creativecommons.org/licenses/by/4.0/
See article on publisher's website: https://dx.doi.org/10.1016/j.mtcomm.2020.101692

Funding

Open Access funding provided by the Qatar National Library

History

Language

  • English

Publisher

Elsevier

Publication Year

  • 2020

License statement

This Item is licensed under the Creative Commons Attribution 4.0 International License

Institution affiliated with

  • Qatar University
  • College of Engineering - QU
  • Biomedical Research Center - QU

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