4.5 Article

Cartilage-targeting drug delivery: can electrostatic interactions help?

Journal

NATURE REVIEWS RHEUMATOLOGY
Volume 13, Issue 3, Pages 183-193

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/nrrheum.2016.210

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Funding

  1. NIH National Institute of Biomedical Imaging and Bioengineering [EB017755]
  2. National Science Foundation Materials Research Science and Engineering Centers (MRSEC) [DMR-1419807]
  3. NIH National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) [AR060331]
  4. Department of Defense (DoD) Congressionally Directed Medical Research Programs (CDMRP) [W81XWH-14-1-0544]

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Current intra-articular drug delivery methods do not guarantee sufficient drug penetration into cartilage tissue to reach cell and matrix targets at the concentrations necessary to elicit the desired biological response. Here, we provide our perspective on the utilization of charge-charge (electrostatic) interactions to enhance drug penetration and transport into cartilage, and to enable sustained binding of drugs within the tissue's highly negatively charged extracellular matrix. By coupling drugs to positively charged nanocarriers that have optimal size and charge, cartilage can be converted from a drug barrier into a drug reservoir for sustained intra-tissue delivery. Alternatively, a wide variety of drugs themselves can be made cartilage-penetrating by functionalizing them with specialized positively charged protein domains. Finally, we emphasize that appropriate animal models, with cartilage thickness similar to that of humans, must be used for the study of drug transport and retention in cartilage.

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