Ramulus mori polysaccharide-loaded PLGA nanoparticles and their anti-inflammatory effects in vivo

Zian Feng1, Song Peng1, Zhiyong Wu2

  • 1Institute of Traditional Chinese Veterinary Medicine, College of Veterinary Medicine, Nanjing Agricultural University, Nanjing 210095, PR China; MOE Joint International Research Laboratory of Animal Health and Food Safety, College of Veterinary Medicine, Nanjing Agricultural University, Nanjing 210095, PR China.

Insights

Ramulus mori polysaccharide (RMP) encapsulated in Poly (lactic-co-glycolicacid) (PLGA) forms PLGA-RMP (PR) nanoparticles. PR demonstrated significant anti-inflammatory effects in a colitis model, improving gut health and microbiota balance.

Area of Science:

  • Biomaterials Science
  • Nanomedicine
  • Gastroenterology

Background:

  • Inflammatory Bowel Disease (IBD) presents significant challenges in treatment.
  • Developing novel therapeutic agents with enhanced efficacy and reduced side effects is crucial.

Purpose of the Study:

  • To investigate the anti-inflammatory effects of Ramulus Mori Polysaccharide (RMP) encapsulated within Poly (lactic-co-glycolicacid) (PLGA) nanoparticles, termed PLGA-RMP (PR).
  • To evaluate the therapeutic potential of PR nanoparticles in a colitis mouse model.

Main Methods:

  • Encapsulation of RMP into PLGA nanoparticles to form PR nanoparticles (average size ~205.6 nm).
  • Administration of PR nanoparticles to a DSS-induced colitis mice model.
  • Assessment of therapeutic effects through body weight, disease activity index (DAI) score, colon length, histopathological analysis, cytokine levels (IFN-γ, IL-6, IL-10), tight junction protein expression (ZO-1, occludin), short-chain fatty acid (SCFA) content, gut microbiota composition, and metabolic profiles.

Main Results:

  • PR nanoparticles significantly attenuated colitis symptoms, including weight loss, DAI score, and colon shortening.
  • Histopathological analysis revealed reduced inflammation, decreased IFN-γ and IL-6, and increased IL-10.
  • PR treatment enhanced tight junction protein expression, improved SCFA levels (acetate, propionate, butyrate), and modulated gut microbiota diversity and composition.
  • PR nanoparticles mitigated metabolic disorders in the colon and reduced the Firmicutes/Bacteroidetes ratio.

Conclusions:

  • PLGA-RMP (PR) nanoparticles exhibit potent anti-inflammatory and therapeutic effects in a colitis model.
  • PR nanoparticles show potential as a nanomedicine for treating IBD and may act as prebiotics by modulating gut microbiota and improving gut barrier function.

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