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Additionally, it was determined that modified scaffolds have proangiogenic activity.
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The molecular design concept of modified scaffolds has been used before to enhance binding affinity of Zn-BDPA structures to small, water-soluble phosphorylated target molecules such as inorganic phosphate, nucleoside polyphosphates, and phosphorylated peptides.
The modified PHBV scaffolds had interconnected pores with porosity of 75.4 78.6% and pore sizes at peak volume from 20 to 50 μm.
The modified scaffolds showed high tendency to induce cell adhesion.
Those modified scaffolds are then ordered and oriented.
The modified scaffolds showed a beta-sheet structure.
PInDI modified scaffolds controlled rhBMP-2 cumulative release.
Fig. 3 PInDI modified scaffolds controlled rhBMP-2 release.
A micro-porous collagen (CL -chondroitin sulfate (CL -chondroitinaffold (Csulfateg. 1A) has been fabriCSted by freeze-drying technique and functionalized with chondroitin sulfate through carbodiimodifiedmiscaffoldg. 1B).
Thus, a physically and chemically modified pNIPAM scaffold had a positive influence on the population of the scaffolds under dynamic culture conditions.
Although nanofibrous scaffolds have many benefits, they are sometimes modified with bioactive molecules using plasma treatment, etching, or γ-ray irradiation to improve the differentiation and mineralization of osteoblasts or mesenchymal stem cells (MSCs) [ 16– 16].
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