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Targeting Strategies for Tissue-Specific Drug Delivery

Journal

CELL
Volume 181, Issue 1, Pages 151-167

Publisher

CELL PRESS
DOI: 10.1016/j.cell.2020.02.001

Keywords

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Funding

  1. NIH
  2. Wyss Institute for Biologically Inspired Engineering

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Off-target effects of systemically administered drugs have been a major hurdle in designing therapies with desired efficacy and acceptable toxicity. Developing targeting strategies to enable sitespecific drug delivery holds promise in reducing off-target effects, decreasing unwanted toxicities, and thereby enhancing a drug's therapeutic efficacy. Over the past three decades, a large body of literature has focused on understanding the biological barriers that hinder tissue-specific drug delivery and strategies to overcome them. These efforts have led to several targeting strategies that modulate drug delivery in both the preclinical and clinical settings, including small molecule-, nucleic acid-, peptide-, antibody-, and cell-based strategies. Here, we discuss key advances and emerging concepts for tissue-specific drug delivery approaches and their clinical translation.

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