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作为定制组织支架材料的静电纺丝脂肪族聚碳酸酯

Electrospun aliphatic polycarbonates as tailored tissue scaffold materials.

作者信息

Welle Alexander, Kröger Mario, Döring Manfred, Niederer Kerstin, Pindel Elvira, Chronakis Ioannis S

机构信息

Forschungszentrum Karlsruhe, Institute for Biological Interfaces (IBG), P.O. Box 3640, 76021 Karlsruhe, Germany.

出版信息

Biomaterials. 2007 Apr;28(13):2211-9. doi: 10.1016/j.biomaterials.2007.01.024. Epub 2007 Jan 16.

Abstract

Two different aliphatic polycarbonates were synthesised from CO(2) and the respective epoxides. Poly(propyl carbonate) (PPC) was prepared by heterogeneous catalysis with zinc glutarate. Poly(cyclohexyl carbonate) (PCHC) was prepared via living copolymerisation homogeneously catalysed by a 3-amino-2-cyanoimidoacrylate zinc acetate complex and subjected to electrospinning. The obtained nanofibres had a well-defined morphology free of beads along the fibres and with slightly porous structures on their surface. Subsequently, low-power deep UV irradiations, previously applied for photochemical surface modifications of two-dimensional and three-dimensional scaffolds from biostable polymers, were performed. Here, an effect on surface and bulk properties of PPC nanofibres was observed. Surface modifications of both polymers affected plasma protein adsorption. Photochemical bulk modifications observed for the first time on PPC nanofibres are indicating the possibility of spatial control of biodegradation rates, hence allow for control of the progression of host/implant interactions in vivo. In particular PPC was used for cell culture of L929 fibroblasts and primary rat hepatocytes. Even delicate primary cells showed good adhesion to the scaffolds and high viability.

摘要

由二氧化碳和相应的环氧化物合成了两种不同的脂肪族聚碳酸酯。聚(碳酸丙酯)(PPC)通过戊二酸锌非均相催化制备。聚(碳酸环己酯)(PCHC)通过由3-氨基-2-氰基亚氨基丙烯酸锌醋酸络合物均相催化的活性共聚制备,并进行静电纺丝。所得纳米纤维具有明确的形态,沿纤维无珠粒,表面具有轻微的多孔结构。随后,进行了低功率深紫外照射,此前该照射已应用于由生物稳定聚合物制成的二维和三维支架的光化学表面改性。在此,观察到对PPC纳米纤维的表面和本体性能的影响。两种聚合物的表面改性均影响血浆蛋白吸附。首次在PPC纳米纤维上观察到的光化学本体改性表明了对生物降解速率进行空间控制的可能性,因此允许控制体内宿主/植入物相互作用的进程。特别是PPC被用于L929成纤维细胞和原代大鼠肝细胞的细胞培养。即使是脆弱的原代细胞也对支架表现出良好的粘附性和高活力。

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