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.
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The data supporting the findings of this study are available within the article and its supplementary information files and from the corresponding author upon reasonable request.
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Work was supported by: JDRF-Juvenile Diabetes Research Foundation Grant 17-2007-1063, National Institutes of Health Grants: DE013023, EB000244, CA151884 and EB000351, Leona M. and Harry B. Helmsley Charitable Trust Foundation Grants: 2015PG-T1D063 and 09PG-T1D027, and through a gift from the Tayebati Family Foundation. J.C.D. was supported by postdoctoral fellowship from JDRF (Fellowship: 3-PDF-2015-91-A-N). J.O. is supported by the Chicago Diabetes Project and the National Institutes of Health (NIH/NIDDK) R01DK091526. G.C.W. is supported by the National Institutes of Health Diabetes Research Centers Grant P30 DK 36836. D.L.G. is supported by the National Institutes of Health (NIH/NIDDK) UC4 DK104218. We acknowledge the use of resources at Core Facilities (Swanson Biotechnology Center, David H. Koch Institute for Integrative Cancer Research at MIT) and W. M. Keck Biological Imaging Facility for Flow Cytometry, Histology, in situ Accelerated Release Microscopy (Wendy C. Salmon, Whitehead Institute), Animal Imaging, and Scanning Electron Microscopy.
The authors declare no competing interests.
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Supplementary Figs. 1–21, Supplementary Video captions 1–3, Supplementary Discussions 1–4 and Supplementary references
In situ monitoring MII and MIII crystals stability and release with fluorescent microscope
Laparoscopic evaluation and 4-week retrievals of implanted ~0.5 mm capsule without drug in non-human primates
Laparoscopic evaluation and 4-week retrievals of implanted ~0.5 mm capsule with GW2580 crystals in non-human primates
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Nature Materials (2019)