Ibuprofen-loaded porous microspheres suppressed the progression of monosodium iodoacetate-induced osteoarthritis in a rat model

Colloids Surf B Biointerfaces. 2016 Nov 1:147:265-273. doi: 10.1016/j.colsurfb.2016.07.050. Epub 2016 Jul 28.

Abstract

The objectives of this study were (1) to fabricate ibuprofen-loaded porous microspheres (IBU/PMSs), (2) to evaluate the in vitro anti-inflammatory effects of the microspheres using LPS-induced inflammation in cultured synoviocytes, and (3) to evaluate the in vivo effect of the IBU/PMSs on the progression of monosodium iodoacetate (MIA)-induced osteoarthritis (OA) in a rat model. A dose-dependent in vitro anti-inflammatory effect on pro-inflammatory cytokine markers (matrix metallopeptidase-3 (MMP-3), matrix metallopeptidase-13 (MMP-13), cyclooxygenase-2 (COX-2), a disintegrin and metalloproteinase with thrombospondin motifs-5 (ADAMTS-5)), interleukin-6 (IL-6), and tumor necrosis factor (TNF-α) was observed by confirming with real-time PCR analyses. In vivo, treatment with IBU/PMSs reduced MIA-stimulated mRNA expression of MMP-3, MMP-13, COX-2, ADAMTS-5, IL-6, and TNF-α in rat synoviocytes. In addition, we demonstrated that intra-articular IBU/PMSs suppressed the progression of MIA-induced OA in the rat model via anti-inflammatory mechanisms. In conclusion, IBU/PMSs are a promising therapeutic material to control the pain and progression of OA.

Keywords: Anti-inflammatory effect; Ibuprofen; Osteoarthritis; PLGA; Porous microspheres.

MeSH terms

  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal / pharmacology*
  • Arthritis, Experimental / chemically induced
  • Arthritis, Experimental / pathology
  • Arthritis, Experimental / prevention & control*
  • Cell Proliferation / drug effects*
  • Chondrocytes / cytology
  • Chondrocytes / drug effects
  • Chondrocytes / metabolism
  • Cyclooxygenase 2 / genetics
  • Cytokines / metabolism
  • Enzyme Inhibitors / toxicity
  • Ibuprofen / pharmacology*
  • Inflammation Mediators / metabolism
  • Iodoacetic Acid / toxicity*
  • Male
  • Matrix Metalloproteinase 13 / genetics
  • Microspheres*
  • Osteoarthritis / chemically induced
  • Osteoarthritis / pathology
  • Osteoarthritis / prevention & control*
  • Rats
  • Real-Time Polymerase Chain Reaction
  • Tumor Necrosis Factor-alpha / genetics

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Cytokines
  • Enzyme Inhibitors
  • Inflammation Mediators
  • Tumor Necrosis Factor-alpha
  • Cyclooxygenase 2
  • MMP13 protein, human
  • Matrix Metalloproteinase 13
  • Iodoacetic Acid
  • Ibuprofen