4.7 Article

Preparation of collagen/hydroxyapatite/alendronate hybrid hydrogels as potential scaffolds for bone regeneration

Journal

COLLOIDS AND SURFACES B-BIOINTERFACES
Volume 143, Issue -, Pages 81-87

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.colsurfb.2016.03.025

Keywords

Hydroxyapatite; Collagen; Alendronate; In situ forming hydrogels; Enzymatically degradable; Bone tissue engineering

Funding

  1. National Natural Science Foundation of China (NSFC) [51103093, 51173126, 81471790, 51473111]
  2. National Science Fund for Distinguished Young Scholars [NSFC 51225302]
  3. Ph.D. Programs Foundation of Ministry of Education of China [20133201110005]
  4. Jiangsu Provincial Special Program of Medical Science [BL2012004]
  5. Priority Academic Program Development (PAPD) of Jiangsu Higher Education Institutions

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Development of biomimetic scaffolds represents a promising direction in bone tissue engineering. In this study, we designed a two-step process to prepare a type of biomimetic hybrid hydrogels that were composed of collagen, hydroxyapatite (HAP) and alendronate (ALN), an anti-osteoporosis drug. First, water-soluble ALN-conjugated HAP (HAP-ALN) containing 4.0 wt.% of ALN was synthesized by treating HAP particles with ALN. Hydrogels were then formed from HAP-ALN conjugate and collagen under physiological conditions using genipin (GNP) as the crosslinker. Depending on the ALN/collagen molar ratio and GNP concentration, the gelation time of hydrogels ranged from 5 to 37 min. Notably, these hybrid hydrogels exhibited markedly improved mechanical property (storage modulus G' = 38-187 kPa), higher gel contents, and lower swelling ratios compared to the hydrogels prepared from collagen alone under similar conditions. Moreover, they showed tunable degradation behaviors against collagenase. The collagen/HAP-ALN hybrid hydrogels supported the adhesion and growth of murine MC3T3-E1 osteoblastic cells well. Such tough yet enzymatically degradable hybrid hydrogels hold potential as scaffolds for bone tissue engineering. (C) 2016 Elsevier B.V. All rights reserved.

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