4.7 Review

Targeting receptor-mediated endocytotic pathways with nanoparticles: Rationale and advances

Journal

ADVANCED DRUG DELIVERY REVIEWS
Volume 65, Issue 1, Pages 121-138

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.addr.2012.09.041

Keywords

Endocytosis; Drug delivery; Cellular targeting; Multivalent targeting

Funding

  1. NIH [RO1 EY016985, R21 EB012281, RO1 EY011386, RO1 EY017293, 5UL1RR031986, R21 CA129388, R21 HL094969]
  2. NSF [0748838]
  3. NATIONAL CANCER INSTITUTE [R21CA129388] Funding Source: NIH RePORTER
  4. NATIONAL CENTER FOR RESEARCH RESOURCES [UL1RR031986] Funding Source: NIH RePORTER
  5. NATIONAL EYE INSTITUTE [R01EY011386, R01EY016985, R01EY017293] Funding Source: NIH RePORTER
  6. NATIONAL HEART, LUNG, AND BLOOD INSTITUTE [R21HL094969] Funding Source: NIH RePORTER
  7. NATIONAL INSTITUTE OF BIOMEDICAL IMAGING AND BIOENGINEERING [R21EB012281] Funding Source: NIH RePORTER

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Targeting of drugs and their carrier systems by using receptor-mediated endocytotic pathways was in its nascent stages 25 years ago. In the intervening years, an explosion of knowledge focused on design and synthesis of nanoparticulate delivery systems as well as elucidation of the cellular complexity of what was previously-termed receptor-mediated endocytosis has now created a situation when it has become possible to design and test the feasibility of delivery of highly specific nanoparticle drug carriers to specific cells and tissue. This review outlines the mechanisms governing the major modes of receptor-mediated endocytosis used in drug delivery and highlights recent approaches using these as targets for in vivo drug delivery of nanoparticles. The review also discusses some of the inherent complexity associated with the simple shift from a ligand-drug conjugate versus a ligand-nanoparticle conjugate, in terms of ligand valency and its relationship to the mode of receptor-mediated internalization. (C) 2012 Elsevier B.V. All rights reserved.

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