Cannabidiol-Loaded Poly Lactic-Co-Glycolic Acid Nanoparticles with Improved Bioavailability as a Potential for Osteoarthritis Therapeutic

Chembiochem. 2023 May 2;24(9):e202200698. doi: 10.1002/cbic.202200698. Epub 2023 Apr 3.

Abstract

Cannabidiol (CBD) is a non-intoxicating cannabinoid from cannabis sativa that has demonstrated efficacious against inflammation, which can be considered as a potential drug for arthritis treatment. However, the poor solubility and low bioavailability limit its clinical application. Here, we report an effective strategy to fabricate Cannabidiol-loaded poly(lactic-co-glycolic acid) copolymer (CBD-PLGA) nanoparticles (NPs), with a spherical morphology and an average diameter of 238 nm. CBD was sustained release from CBD-PLGA-NPs, which improved the bioavailability of CBD. The CBD-PLGA-NPs effectively protect the damage of LPS to cell viability. We observed that CBD-PLGA-NPs significantly suppressed LPS-induced primary rat chondrocyte expression of inflammatory cytokines, including interleukin 1β (IL-1β), interleukin 6 (IL-6), tumor necrosis factor-α (TNF-α) and matrix metalloproteinase 13 (MMP-13). Remarkably, CBD-PLGA-NPs also showed better therapeutic effects of inhibiting the degradation of the extracellular matrix of chondrocytes than equivalent CBD solution. In general, the fabrication CBD-PLGA-NPs showed good protection of primary chondrocytes in vitro and is a promising system for osteoarthritis treatment.

Keywords: anti-inflammatory; cannabidiol; chondrocytes; nanoparticles; osteoarthritis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biological Availability
  • Cannabidiol* / pharmacology
  • Cannabidiol* / therapeutic use
  • Drug Carriers
  • Glycols
  • Lipopolysaccharides
  • Nanoparticles*
  • Osteoarthritis* / drug therapy
  • Polylactic Acid-Polyglycolic Acid Copolymer
  • Rats

Substances

  • Cannabidiol
  • Glycols
  • glycolic acid
  • Lipopolysaccharides
  • Polylactic Acid-Polyglycolic Acid Copolymer
  • Drug Carriers