Table 3.
Enumeration of devices containing macroencapsulated islets being used in various preclinical and clinical trials.
Name of device | Pre-clinical/clinical trials | Design advantage | Reference(s) |
---|---|---|---|
β-Air | Transplantation of porcine islets into monkeys Clinical trial with human islets transplanted into humans |
Promises adequate oxygen supply and comparatively improved protection from recipient immune system | (80, 81) |
3D printed vascularized device | Transplantation of human islets in mice | Contains growth factors for optimized vascularization of islets | (82) |
Bioplotted scaffold | Transplantation of human islets into mice without immunosuppression | Enhanced vascularization and efficient diffusion owing to adjustable pore size; also avoids islet clumping | (83) |
Silicon nanopore membrane device | Mouse islets into pig islets | Adequate pore size (10 nm) and more cell viability | (84) |
TheraCyte | Lewis rats were islet donors, and alloimmunized, diabetic Wistar–Furth rats were used as recipients | More vascularization and optimum inner membrane pore size (0.4 μm) to embargo immune response | (85) |
Encaptra | Implantation of pancreatic progenitor cells into mice. Clinical trial: implantation of pancreatic progenitor cells into humans | The device allows the growth of pancreatic progenitor cells | (86) |