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Gas anti-solvent precipitation assisted salt leaching for generation of micro- and nano-porous wall in bio-polymeric 3D scaffolds

机译:气体反溶剂沉淀辅助盐浸法可在生物聚合3D支架中生成微孔和纳米孔壁

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摘要

The mass transport through biocompatible and biodegradable polymeric 3D porous scaffolds may be depleted by non-porous impermeable internal walls. As consequence the concentration of metabolites and growth factors within the scaffold may be heterogeneous leading to different cell fate depending on spatial cell location, and in some cases it may compromise cell survival. In this work, we fabricated polymeric scaffolds with micro- and nano-scale porosity by developing a new technique that couples two conventional scaffold production methods: solvent casting-salt leaching and gas antisolvent precipitation. 10-15 w/w solutions of a hyaluronic benzyl esters (HYAFF11) and poly-(Iactic acid) (PLA) were used to fill packed beds of 0.177-0.425 mm NaCl crystals. The polymer precipitation in micro and nano-porous structures between the salt crystals was induced by high-pressure gas, then its flushing extracted the residual solvent. The salt was removed by water-wash. Morphological analysis by scanning electron microscopy showed a uniform porosity (-70%) and a high interconnectivity between porous. The polymeric walls were porous themselves counting for 30% of the total porosity. This wall porosity did not lead to a remarkable change in compressive modulus, deformation, and rupture pressure. Scaffold biocom-patibility was tested with murine muscle cell line C2C12 for 4 and 7 days. Viability analysis and histology showed that micro- and nano-porous scaffolds are biocompatible and suitable for 3D cell culture promoting cell adhesion on the polymeric wall and allowing their proliferation in layers. Micro- and nano-scale porosities enhance cell migration and growth in the inner part of the scaffold.
机译:通过生物相容性和可生物降解的聚合物3D多孔支架的大量运输可能会被无孔的不渗透内壁所消耗。结果,支架中代谢物和生长因子的浓度可能是异质的,这取决于空间细胞位置,导致不同的细胞命运,在某些情况下,它可能会损害细胞存活率。在这项工作中,我们通过开发一种结合了两种传统支架生产方法的新技术,制造了具有微米级和纳米级孔隙率的聚合物支架,这两种方法分别是:溶剂浇铸-盐浸和气体反溶剂沉淀。透明质酸苄酯(HYAFF11)和聚(乳酸)(PLA)的10-15 w / w溶液用于填充0.177-0.425 mm NaCl晶体的填充床。高压气体诱导盐晶体之间的微孔和纳米孔结构中的聚合物沉淀,然后冲洗除去残余溶剂。通过水洗除去盐。通过扫描电子显微镜的形态分析显示均匀的孔隙率(-70%)和多孔之间的高互连性。聚合物壁本身是多孔的,占总孔隙率的30%。该壁的孔隙率并未导致压缩模量,变形和破裂压力的显着变化。用鼠肌细胞系C2C12测试支架生物相容性4天和7天。生存力分析和组织学研究表明,微孔和纳米孔支架具有生物相容性,适用于3D细胞培养,可促进细胞在聚合物壁上的粘附并使其分层扩散。微米和纳米级的孔隙度增强了支架内部细胞的迁移和生长。

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