4.7 Article

Hyaluronic acid oligosaccharide-collagen mineralized product and aligned nanofibers with enhanced vascularization properties in bone tissue engineering

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ELSEVIER
DOI: 10.1016/j.ijbiomac.2022.02.148

关键词

Hyaluronic acid oligosaccharide; Collagen; Anisotropic nanofiber; Mineralized microparticles; Vascularization; Bone tissue engineering

资金

  1. Technology Development Project of Shandong Province of China [2017GSF18119]
  2. Central Government Guide Local Science and Technology Development Funds [YDZX20203700002579]

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Considering the complexity and limitations of current treatment options for bone defects, designing a biomimetic and functional tissue-engineered bone graft is urgently needed. In this study, an engineered bone scaffold based on aligned nanofibers and mineralized microparticles was developed to guide cell-specific orientation and osseointegration in bone healing. The scaffold exhibited ideal biocompatibility and tissue regenerative capacity, making it a promising candidate for bone tissue engineering applications.
Considering the structural complexity of natural bone and the limitations of current treatment options, designing a biomimetic and functional tissue-engineered bone graft has been an urgent need for the replacement and regeneration of defected bone tissue. In light of the cell recruitment to the defect region, scaffold-guided bone tissue engineering has proven to be a viable strategy that is poised to deliver effective osseointegration and vascularization during bone remodeling. Herein, we provide an engineered bone scaffold based on aligned poly (lactic-co-glycolide) (PLGA) nanofibers incorporated with hyaluronic acid oligosaccharide-collagen mineralized microparticles (labeled oHA-Col/HAP) to guide the cell-specific orientation and osseointegration in bone healing. The aligned nanofibers were successfully prepared by a custom-made rotating mandrel with separating railings and HAs-Col/HAP mineralized microparticles were uniformly distributed in the composite scaffolds that acted as temporary templates for bone remodeling. The morphology, physicochemical properties and tensile strength of the scaffolds were characterized, the cell responses and in vivo biocompatibility and biodegradability of the scaffolds were also studied to evaluate the potential for bone tissue engineering. The experimental results illustrated that such anisotropic scaffolds loaded with oHA-Col/HAP microparticles mediated cell orderly arrangement conducive to the migration and recruitment of osseointegration-related cells and were stimulatory of cell proliferation. Those oHA-Col/HAP@PLGA scaffolds exhibited ideal biocompatibility and tissue regenerative capacity in vivo through a higher expression of vascularization-related genes. Overall, the novel engineered bone scaffold promises to serve as alternative candidates for bone tissue engineering applications.

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