AI Article Synopsis

  • Hydroxy-safflower yellow A (HYSA), a component of traditional Chinese medicine, has not been thoroughly studied for its potential benefits in bone healing through osteogenesis and angiogenesis.
  • Researchers developed synthetic bioactive glass scaffolds coated with chitosan/sodium alginate to deliver HYSA, which greatly improved mechanical strength and provided controlled drug release.
  • In laboratory and animal studies, high doses of HYSA-loaded scaffolds significantly enhanced bone cell proliferation and new bone formation compared to scaffolds without HYSA, suggesting their potential as effective biomaterials for bone regeneration.

Article Abstract

Some traditional Chinese medicine (TCM) has been applied in bone repair, however, hydroxy-safflower yellow A (HYSA), one composition of safflower of the typical invigorating the circulation of TCM, has little been studied in orthopedics field for osteogenesis and angiogenesis clinically. Herein, we hypothetically speculated that the synthetic bioactive glasses (BG, 1393) scaffolds carried HYSA by a 3D print technique could enhance osteogenic repair properties. Notably, scaffolds coating chitosan/sodium alginate endowed with excellent drug control release ability, and significantly improved the BG mechanical strength. HYSA was loaded into BG scaffolds by coating chitosan/sodium alginate film, and the osteogenesis and angiogenesis of the HYSA/scaffolds were evaluated in vitro and in vivo. In vitro the cell culture results exhibited that the high dose of HYSA (0.5 mg/ml) loaded scaffolds can promote the proliferation of bone marrow stromal cells (rBMSCs) and migration, tubule formation of human umbilical vein endothelial cells (HUVECs). The active alkaline phosphatase (ALP) of rBMSCs can also be improved by the high dose of HYSA/scaffolds. Results of qRT-PCR and Western blot indicated that the high dose of HYSA/scaffolds can up-regulate ALP, OCN, OPN and RUNX-2 expression and relative protein secretion of the HIF-1α and BMP-2. In the animal experiment, the high dose of HYSA/scaffolds has a significantly better capacity to promote new bone formation than the undoped scaffolds at 8 weeks post-surgery. Thus, our results claimed that the novel HYSA/scaffolds hold the substantial potential to be further developed as effective and safe bone tissue engineering biomaterials for bone regeneration by combining enhanced osteogenesis and angiogenesis.

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Source
http://dx.doi.org/10.1016/j.yexcr.2020.112139DOI Listing

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