Fabrication and characterization of apigenin-loaded chitosan/gelatin membranes for bone tissue engineering applications

被引:8
作者
Bozorgi, Azam [1 ,2 ]
Khazaei, Mozafar [2 ]
Bozorgi, Maryam [2 ]
Jamalpoor, Zahra [3 ]
机构
[1] Kermanshah Univ Med Sci, Sch Med, Dept Tissue Engn, Kermanshah, Iran
[2] Kermanshah Univ Med Sci, Hlth Technol Inst, Fertil & Infertil Res Ctr, Kermanshah, Iran
[3] AJA Univ Med Sci, Trauma Res Ctr, Tehran, Iran
关键词
Bone tissue engineering; chitosan; gelatin membrane; apigenin; osteoblast proliferation; mineralization; PROMOTES OSTEOGENIC DIFFERENTIATION; MESENCHYMAL STEM-CELLS; MORPHOGENETIC PROTEIN-2; OSTEOCLASTOGENESIS; SCAFFOLDS; JNK;
D O I
10.1177/08839115221149725
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Fabricating degradable polymer-based membranes has attracted much attention for guided bone regeneration. Chitosan/gelatin (Cs/Gel) composites are among the most known scaffolds with structural similarity to bone matrix and a high potential to support cell attachment and proliferation. Recently, plant-derived phenolic compound apigenin has been identified to direct the osteogenic differentiation of mesenchymal stem cells and retain osteoblast metabolic functions. We incorporated apigenin into Cs/Gel membranes to improve apigenin bioavailability and get proper concentrations for efficient biological activities. Apigenin-loaded Cs/Gel membranes were prepared using a solution casting method with various apigenin contents (0, 10, 25, 50, and 100 mu M). Chemical composition, morphological characteristics, swelling behavior, degradation rate, and apigenin release from membranes were evaluated. Saos-2 osteoblasts were cultured on membranes to investigate cell-membrane interaction, proliferation, viability, and mineralization under the osteogenic culture condition. The results showed that membranes had homogeneous and moderate rough surfaces, facilitating osteoblast attachment and expansion. Swelling ratios exceeded 200%, reaching a stable rate in 24 h. Apigenin-loaded membranes degraded slower in vitro. Membranes containing lower apigenin concentrations exhibited a higher cargo release profile over 21 days. Apigenin improved osteoblast proliferation and viability, but the mineralization depended on apigenin dose, with optimized values at low concentrations. These data suggested that Cs/Gel membranes loaded with low apigenin contents improved osteoblast survival, proliferation, and mineralization.
引用
收藏
页码:142 / 157
页数:16
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