J
Jason A. Burdick
Researcher at University of Pennsylvania
Publications - 363
Citations - 42498
Jason A. Burdick is an academic researcher from University of Pennsylvania. The author has contributed to research in topics: Self-healing hydrogels & Tissue engineering. The author has an hindex of 103, co-authored 335 publications receiving 34137 citations. Previous affiliations of Jason A. Burdick include Duke University & University of Kentucky.
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Journal ArticleDOI
Mechanically robust and bioadhesive collagen and photocrosslinkable hyaluronic acid semi-interpenetrating networks.
Mark D. Brigham,Alexander G. Bick,Edward Lo,Amel Bendali,Jason A. Burdick,Ali Khademhosseini +5 more
TL;DR: A class of hydrogels that leverage the favorable properties of the photo-cross-linkable hyaluronic acid (HA) and semi-interpenetrating collagen components and far surpass those achievable with collagen gels or collagen gel-based semi-IPNs are presented.
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Sequential crosslinking to control cellular spreading in 3-dimensional hydrogels
TL;DR: A novel process that utilizes different crosslinking mechanisms to provide gel environments that are either permissive or inhibitory to cellular spreading is developed, both to provide new insights into the relationships between gel structure and cell behavior, and for eventual tissue-engineering applications where spatial control over cells is desired.
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3D bioprinting of high cell-density heterogeneous tissue models through spheroid fusion within self-healing hydrogels
TL;DR: In this paper, the authors developed a bioprinting approach to transfer spheroids into self-healing support hydrogels at high resolution, which enables their patterning and fusion into high-cell density microtissues of prescribed spatial organization.
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Matrix degradability controls multicellularity of 3D cell migration.
Britta Trappmann,Britta Trappmann,Brendon M. Baker,Brendon M. Baker,William J. Polacheck,William J. Polacheck,Colin K. Choi,Colin K. Choi,Jason A. Burdick,Christopher S. Chen,Christopher S. Chen +10 more
TL;DR: An in vitro model whereby molded tubular channels inside a synthetic hydrogel are seeded with endothelial cells and subjected to chemokine gradients within a microfluidic device is developed and it is found that matrix degradability modulates the collectivity of cell migration.
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Hydrolytically Degradable Hyaluronic Acid Hydrogels with Controlled Temporal Structures
TL;DR: For the first time, a new macromer allows for enhanced control over the structural evolution of the HA hydrogels toward applications as biomaterials.