378549 Injectable Hydrogels with in Situ Double-Network Formation for Cell Transplantation

Monday, November 17, 2014: 3:47 PM
International 7 (Marriott Marquis Atlanta)
Lei Cai, Ruby E. Dewi and Sarah C. Heilshorn, Materials Science and Engineering, Stanford University, Stanford, CA

Cell transplantation via direct cell injection at the target site is a minimally invasive strategy for treating various injuries and degenerative diseases. However, cell viability is typically only 5% in these procedures, and the therapeutic success critically hinges on the survival and subsequent maintenance of the transplanted cells. To protect these cells, we designed an injectable hydrogel that undergoes two different physical crosslinking mechanisms. The first crosslinking step occurs ex vivo through peptide-based molecular recognition to encapsulate cells within a physical hydrogel, while the second crosslinking step occurs in situ through a thermal phase transition to form a reinforcing network.  At room temperature, the physical hydrogel is shear-thinning and self-healing to facilitate gentle cell encapsulation and transplantation by syringe injection. At body temperature, the hydrogel forms a secondary network resulting in a 10-fold increase in shear modulus and significantly reduced erosion rates and prolonged retention time. Human adipose-derived stromal cells (hASCs) injected through a 28-gauge syringe needle were significantly protected from disruptive mechanical forces when encapsulated within the hydrogel compared to medium alone. In vivo subcutaneous injection of hASCs in a murine model demonstrated significantly improved cell retention when delivered in a double-network hydrogel compared to a single-network gel or medium alone. These results suggest that in situ formation of a reinforcing network within an already existing hydrogel can enhance mechanical properties and retention time, and thereby improve long-term cell viability. These cell-delivery materials are being further investigated for the ability to support functional tissue regeneration at sites of ischemia.

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