Evaluating intra-articular drug delivery for the treatment of osteoarthritis in a rat model.

Journal Article (Journal Article;Review)

Osteoarthritis (OA) is a degenerative joint disease that can result in joint pain, loss of joint function, and deleterious effects on activity levels and lifestyle habits. Current therapies for OA are largely aimed at symptomatic relief and may have limited effects on the underlying cascade of joint degradation. Local drug delivery strategies may provide for the development of more successful OA treatment outcomes that have potential to reduce local joint inflammation, reduce joint destruction, offer pain relief, and restore patient activity levels and joint function. As increasing interest turns toward intra-articular drug delivery routes, parallel interest has emerged in evaluating drug biodistribution, safety, and efficacy in preclinical models. Rodent models provide major advantages for the development of drug delivery strategies, chiefly because of lower cost, successful replication of human OA-like characteristics, rapid disease development, and small joint volumes that enable use of lower total drug amounts during protocol development. These models, however, also offer the potential to investigate the therapeutic effects of local drug therapy on animal behavior, including pain sensitivity thresholds and locomotion characteristics. Herein, we describe a translational paradigm for the evaluation of an intra-articular drug delivery strategy in a rat OA model. This model, a rat interleukin-1beta overexpression model, offers the ability to evaluate anti-interleukin-1 therapeutics for drug biodistribution, activity, and safety as well as the therapeutic relief of disease symptoms. Once the action against interleukin-1 is confirmed in vivo, the newly developed anti-inflammatory drug can be evaluated for evidence of disease-modifying effects in more complex preclinical models.

Full Text

Duke Authors

Cited Authors

  • Allen, KD; Adams, SB; Setton, LA

Published Date

  • February 2010

Published In

Volume / Issue

  • 16 / 1

Start / End Page

  • 81 - 92

PubMed ID

  • 19943805

Pubmed Central ID

  • PMC2817653

Electronic International Standard Serial Number (EISSN)

  • 1937-3376

Digital Object Identifier (DOI)

  • 10.1089/ten.teb.2009.0447


  • eng

Conference Location

  • United States