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Enhancing the mechanical properties and physical stability of biomimetic polymer hydrogels for micro-patterning and tissue engineering applications

机译:增强仿生聚合物水凝胶在微图案和组织工程应用中的机械性能和物理稳定性

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Low mechanical strength and rapid degradation of photo-crosslinkable polymers are the major obstacles for their applications. The aim of this study was to address these issues by fabricating hybrid polymeric hydrogels from a biopolymer (gelatin) and a synthetic polymer. Methacrylated gelatin (GelMA) and poly(lactic-ethylene oxide fumarate) (PLEOF) were photo-crosslinked, using Irgacure and poly(ethylene glycol)-diacrylate. The optimum hybrid hydrogel was produced when using 200 mg/ml PLEOF and 100 mg/ml GelMA. These hydrogels possessed porosity in the range of 90%, also comprised of micro (~20 lm) and macro pores (540 lm), which are suitable for nutrients mass transfer and osteoblast cell proliferation, respectively. The compression modulus of GelMA-PLEOF hydrogels was more than 200 kPa, which is paramount compared to GelMA hydrogels. Moreover, fabrication of hybrid hydrogel substantially enhanced the structural stability of gelatin in simulated physiological environment from one week to more than 28 days. In vitro studies showed that primary human osteoblast cells adhered and proliferated into PLEOF/GelMA hydrogel. Additionally, micro-patterns with 10 x 100 μm dimensions were created on the surface of these hydrogels to promote the cellular alignment. These results demonstrated the potential of using this hybrid construct for in vitro regeneration of load-bearing tissues.
机译:机械强度低和光可交联聚合物的快速降解是其应用的主要障碍。这项研究的目的是通过由生物聚合物(明胶)和合成聚合物制造杂化聚合物水凝胶来解决这些问题。使用Irgacure和聚(乙二醇)-二丙烯酸酯对甲基丙烯酸酯化的明胶(GelMA)和聚(乳酸-环氧乙烷富马酸酯)(PLEOF)进行光交联。当使用200 mg / ml PLEOF和100 mg / ml GelMA时,可产生最佳的杂化水凝胶。这些水凝胶的孔隙率在90%的范围内,还包括微孔(〜20 lm)和大孔(540 lm),分别适合营养物质的传质和成骨细胞的增殖。 GelMA-PLEOF水凝胶的压缩模量大于200 kPa,这与GelMA水凝胶相比至关重要。此外,杂化水凝胶的制备从模拟的生理环境中将明胶的结构稳定性从一周提高到了超过28天。体外研究表明,人类原代成骨细胞粘附并增殖为PLEOF / GelMA水凝胶。另外,在这些水凝胶的表面上创建了尺寸为10 x 100μm的微图案,以促进细胞排列。这些结果证明了使用这种杂合构建体在承重组织的体外再生中的潜力。

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