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      Challenges in design of translational nanocarriers

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      Journal of Controlled Release
      Elsevier BV

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          Abstract

          Cancer drug delivery achieving high therapeutic efficacy and low side effects requires a nanocarrier to tightly retain the drug, efficiently reach the tumor, then quickly enter the tumor cells and release the drug. Furthermore, the nanocarrier intended for clinical applications should use materials safe as pharmaceutical excipients and its formulation (nanomedicine) should have good manufacture processes with scale-up ability. Thus, the challenge is to design safe, approvable, and easily scaled-up nanocarriers that simultaneously meet the two pairs of requirements of 'drug retention in circulation versus intracellular release' and 'stealthy in circulation versus sticky (cell-binding) in tumor' at the right places in order to deliver a cytosolic drug dose lethal to cancer cells with minimized side effects. Herein, we briefly review these elements aimed at promoting developments of translational nanocarriers.

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          Author and article information

          Journal
          Journal of Controlled Release
          Journal of Controlled Release
          Elsevier BV
          01683659
          December 2012
          December 2012
          : 164
          : 2
          : 156-169
          Article
          10.1016/j.jconrel.2012.05.042
          22664472
          1bf6172e-86ec-49fb-b734-e4ed0881dd52
          © 2012

          http://www.elsevier.com/tdm/userlicense/1.0/

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