4.8 Article

Biodegradable, phosphate-containing, dual-gelling macromers for cellular delivery in bone tissue engineering

Journal

BIOMATERIALS
Volume 67, Issue -, Pages 286-296

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.biomaterials.2015.07.016

Keywords

Hydrogel; Poly(N-isopropyl acrylamide); Monoacryloxyethyl phosphate; Rat cranial defect; Mesenchymal stem cell encapsulation

Funding

  1. National Institutes of Health [R01 DE17441, R01 AR48756]
  2. Keck Center Nanobiology Training Program of the Gulf Coast Consortia (NIH) [T32 EB009379]
  3. Baylor College of Medicine Medical Scientist Training Program [NIH T32 GM007330]

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Injectable, biodegradable, dual-gelling macromer solutions were used to encapsulate mesenchymal-stem cells (MSCs) within stable hydrogels when elevated to physiologic temperature. Pendant phosphate groups were incorporated in the N-isopropyl acrylamide-based macromers to improve biointegration and facilitate hydrogel degradation. The MSCs were shown to survive the encapsulation process, and live cells were detected within the hydrogels for up to 28 days in vitro. Cell-laden hydrogels were shown to undergo significant mineralization in osteogenic medium. Cell-laden and acellular hydrogels were implanted into a critical-size rat cranial defect for 4 and 12 weeks. Both cell-laden and acellular hydrogels were shown to degrade in vivo and help to facilitate bone growth into the defect. Improved bone bridging of the defect was seen with the incorporation of cells, as well as with higher phosphate content of the macromer. Furthermore, direct bone-to-hydrogel contact was observed in the majority of implants, which is not commonly seen in this model. The ability of these macromers to deliver stem cells while forming in situ and subsequently degrade while facilitating bone ingrowth into the defect makes this class of macromers a promising material for craniofacial bone tissue engineering. (C) 2015 Elsevier Ltd. All rights reserved.

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