Long-term implant fibrosis prevention in rodents and non-human primates using crystallized drug formulations

  • Shady Farah
  • , Joshua C. Doloff
  • , Peter Müller
  • , Atieh Sadraei
  • , Hye Jung Han
  • , Katy Olafson
  • , Keval Vyas
  • , Hok Hei Tam
  • , Jennifer Hollister-Lock
  • , Piotr S. Kowalski
  • , Marissa Griffin
  • , Ashley Meng
  • , Malia McAvoy
  • , Adam C. Graham
  • , James McGarrigle
  • , Jose Oberholzer
  • , Gordon C. Weir
  • , Dale L. Greiner
  • , Robert Langer
  • , Daniel G. Anderson

Research output: Contribution to journalArticlepeer-review

Abstract

Implantable medical devices have revolutionized modern medicine. However, immune-mediated foreign body response (FBR) to the materials of these devices can limit their function or even induce failure. Here we describe long-term controlled-release formulations for local anti-inflammatory release through the development of compact, solvent-free crystals. The compact lattice structure of these crystals allows for very slow, surface dissolution and high drug density. These formulations suppress FBR in both rodents and non-human primates for at least 1.3 years and 6 months, respectively. Formulations inhibited fibrosis across multiple implant sites—subcutaneous, intraperitoneal and intramuscular. In particular, incorporation of GW2580, a colony stimulating factor 1 receptor inhibitor, into a range of devices, including human islet microencapsulation systems, electrode-based continuous glucose-sensing monitors and muscle-stimulating devices, inhibits fibrosis, thereby allowing for extended function. We believe that local, long-term controlled release with the crystal formulations described here enhances and extends function in a range of medical devices and provides a generalized solution to the local immune response to implanted biomaterials.

Original languageEnglish
Pages (from-to)892-904
Number of pages13
JournalNature Materials
Volume18
Issue number8
DOIs
Publication statusPublished - 1 Aug 2019
Externally publishedYes

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