4.8 Review

Endocytosis of nanomedicines

期刊

JOURNAL OF CONTROLLED RELEASE
卷 145, 期 3, 页码 182-195

出版社

ELSEVIER
DOI: 10.1016/j.jconrel.2010.01.036

关键词

Endocytosis; Nanomedicines; Nanoparticles; Intracellular trafficking; Caveolae; Clathrin

资金

  1. National Institutes of Health [CA89225, CA116591, NS051334, 1P20RR021937]
  2. Department of Defense [W81XWH-09-1-0386, USAMRMC 06108004]
  3. UNMC

向作者/读者索取更多资源

Novel nanomaterials are being developed to improve diagnosis and therapy of diseases through effective delivery of drugs, biopharmaceutical molecules and imaging agents to target cells in disease sites. Such diagnostic and therapeutic nanomaterials, also termed nanomedicines, often require site-specific cellular entry to deliver their payload to sub-cellular locations hidden beneath cell membranes. Nanomedicines can employ multiple pathways for cellular entry, which are currently insufficiently understood. This review,first, classifies various mechanisms of endocytosis available to nanomedicines including phagocytosis and pinocytosis through clathrin-dependent and clathrin-independent pathways. Second, it describes the current experimental tools to study endocytosis of nanomedicines. Third, it provides specific examples from recent literature and our own work on endocytosis of nanomedicines. Finally, these examples are used to ascertain 1) the role of particle size, shape, material composition, surface chemistry and/or charge for utilization of a selected pathway(s); 2) the effect of cell type on the processing of nanomedicines; and 3) the effect of nanomaterial-cell interactions on the processes of endocytosis, the fate of the nanomedicines and the resulting cellular responses. This review will be useful to a diverse audience of students and scientists who are interested in understanding endocytosis of nanomedicines. (c) 2010 Elsevier B.V. All rights reserved.

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