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Polymer Microparticles Prolong Delivery of the 15-PGDH Inhibitor SW033291.

Alan B DoganNathan A RohnerJulianne N P SmithJessica A KilgoreNoelle S WilliamsSanford D MarkowitzHorst A von RecumAmar B Desai
Published in: Pharmaceutics (2021)
As the prevalence of age-related fibrotic diseases continues to increase, novel antifibrotic therapies are emerging to address clinical needs. However, many novel therapeutics for managing chronic fibrosis are small-molecule drugs that require frequent dosing to attain effective concentrations. Although bolus parenteral administrations have become standard clinical practice, an extended delivery platform would achieve steady-state concentrations over a longer time period with fewer administrations. This study lays the foundation for the development of a sustained release platform for the delivery of (+)SW033291, a potent, small-molecule inhibitor of the 15-hydroxyprostaglandin dehydrogenase (15-PGDH) enzyme, which has previously demonstrated efficacy in a murine model of pulmonary fibrosis. Herein, we leverage fine-tuned cyclodextrin microparticles-specifically, β-CD microparticles (β-CD MPs)-to extend the delivery of the 15-PGDH inhibitor, (+)SW033291, to over one week.
Keyphrases
  • small molecule
  • pulmonary fibrosis
  • clinical practice
  • protein protein
  • high throughput
  • air pollution
  • systemic sclerosis
  • clinical trial
  • drug induced
  • nk cells
  • anti inflammatory