Angiogenic biomaterials for cell delivery
The subcutaneous space has been pursued as an alternative site for islet transplantation, however hypoxic conditions experienced during revascularization has resulted in islet loss.
To reduce the therapeutic dosage, we highlight a biomaterial-based approach using a methacrylic acid copolymer coating to generate a robust pre-vascularized subcutaneous cavity for islet transplantation.
In addition, we devised a simple, but not-trivial, procedure for filling the cavity with an islet suspension in collagen.
We showed that the pre-vascularized cavity supported a marginal mass of islets in pre-clinical diabetic models of mice and rats.
For more information, check out our 2021 publication in Biomaterials.
Here we report the preparation of a semi-interpenetrating polymer network (SIPN), and its evaluation as an injectable carrier to deliver cells and generate blood vessels in a subcutaneous implantation site.
The SIPN was prepared by reacting a blend of vinyl sulfone-terminated polyethylene glycol (PEG-VS) and sodium polymethacrylate (PMAA-Na) with dithiothreitol.
SIPN containing 20 mol% PMAA-Na generated a vascular network in the surrounding tissues, with 2–3 times as many vessels as was obtained with 10 mol% PMAA-Na or PEG alone.
Using a streptozotocin-induced diabetic mouse model we validated the potential to use SIPN to deliver pancreatic islets into the subcutaneous space and return them to normoglycemic levels.
Furthermore, transplanted islets were revascularized and reinnervated by day 70 in host-derived subcutaneous tissues.
For more information, please read our 2017, 2022, and 2023 work in Biomaterials.