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Gas-Foaming Calcium Phosphate Cement Scaffold Encapsulating Human Umbilical Cord Stem Cells

机译:气体发泡磷酸钙水泥支架包封人脐带干细胞。

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摘要

Tissue engineering approaches are promising to meet the increasing need for bone regeneration. Calcium phosphate cement (CPC) can be injected and self-set to form a scaffold with excellent osteoconductivity. The objectives of this study were to develop a macroporous CPC–chitosan–fiber construct containing alginate–fibrin microbeads encapsulating human umbilical cord mesenchymal stem cells (hUCMSCs) and to investigate hUCMSC release from the degrading microbeads and proliferation inside the porous CPC construct. The hUCMSC-encapsulated microbeads were completely wrapped inside the CPC paste, with the gas-foaming porogen creating macropores in CPC to provide for access to culture media. Increasing the porogen content in CPC significantly increased the cell viability, from 49% of live cells in CPC with 0% porogen to 86% of live cells in CPC with 15% porogen. The alginate–fibrin microbeads started to degrade and release the cells inside CPC at 7 days. The released cells started to proliferate inside the macroporous CPC construct. The live cell number inside CPC increased from 270 cells/mm2 at 1 day to 350 cells/mm2 at 21 days. The pore volume fraction of CPC increased from 46.8% to 78.4% using the gas-foaming method, with macropore sizes of approximately 100 to 400 μm. The strength of the CPC–chitosan–fiber scaffold at 15% porogen was 3.8 MPa, which approximated the reported 3.5 MPa for cancellous bone. In conclusion, a novel gas-foaming macroporous CPC construct containing degradable alginate–fibrin microbeads was developed that encapsulated hUCMSCs. The cells had good viability while wrapped inside the porous CPC construct. The degradable microbeads in CPC quickly released the cells, which proliferated over time inside the porous CPC. Self-setting, strong CPC with alginate–fibrin microbeads for stem cell delivery is promising for bone tissue engineering applications.
机译:组织工程学方法有望满足不断增长的骨骼再生需求。可以注射磷酸钙水泥(CPC)并自固化以形成具有出色骨传导性的支架。这项研究的目的是开发包含藻酸盐-纤维蛋白微珠的大孔CPC-壳聚糖-纤维构建体,该微囊包封人脐带间充质干细胞(hUCMSCs),并研究hUCMSC从降解微珠释放以及在多孔CPC构建体内的增殖。将hUCMSC封装的微珠完全包裹在CPC糊剂中,用发泡泡沫的致孔剂在CPC中产生大孔,以提供进入培养基的通道。增加CPC中的致孔剂含量会显着提高细胞活力,从含0%致孔剂的CPC中49%的活细胞到含有15%致孔剂的CPC中86%的活细胞。 7天时,藻酸盐-纤维蛋白微珠开始降解并释放CPC内的细胞。释放的细胞开始在大孔CPC构建体中增殖。 CPC中的活细胞数量从第1天的270个细胞/ mm 2 增加到第21天的350个细胞/ mm 2 。使用气体发泡法,CPC的孔体积分数从46.8%增加到78.4%,大孔尺寸大约为100至400μm。 CPC-壳聚糖-纤维支架在成孔剂为15%时的强度为3.8 MPa,大约相当于所报道的松质骨的3.5 MPa。总之,开发了一种新型的气体发泡大孔CPC构建体,其中包含可降解的藻酸盐-血纤蛋白微珠,并封装了hUCMSC。这些细胞被包裹在多孔CPC结构中时具有良好的生存能力。 CPC中的可降解微珠迅速释放了细胞,这些细胞随着时间的推移在多孔CPC中增殖。具有海藻酸盐-血纤蛋白微珠的自定性强CPC可以用于干细胞递送,有望用于骨组织工程应用。

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