Publication: Long-Term Implant Fibrosis Prevention in Rodents and Non-Human Primates Using Localized Deliverable Crystals
No Thumbnail Available
Open/View Files
Date
2019-06-24
Published Version
Journal Title
Journal ISSN
Volume Title
Publisher
Nature Publishing Group
The Harvard community has made this article openly available. Please share how this access benefits you.
Citation
Farah, Shady, Joshua Doloff, Peter Müller, Atieh Sadraei, Katy Olafson, Keval Vyas, Hok Tam, Jennifer Hollister-Lock, Piotr Kowalski, Marissa Griffin, Ashley Meng, Malia McAvoy, Adam Graham, James McGarrigle, Jose Oberholzer, Gordon Weir, Dale Greiner, Robert Langer, and Daniel Anderson. 2019. Long-term Implant Fibrosis Prevention in Rodents and Non-human Primates Using Crystallized Drug Formulations. Nature Materials 18, no. 8: 892-904.
Research Data
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 (CSF1R) 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.
Description
Other Available Sources
Keywords
Terms of Use
Metadata Only