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采用纳米纤维双组分支架进行神经组织工程的双重生长因子的复合和释放。

Incorporation and release of dual growth factors for nerve tissue engineering using nanofibrous bicomponent scaffolds.

机构信息

Department of Mechanical Engineering, The University of Hong Kong, Pokfulam Road, Hong Kong, People's Republic of China. Department of Research and Development, Shenzhen Gene Health Bio Tech Co., Ltd, Shenzhen, 518055, People's Republic of China.

出版信息

Biomed Mater. 2018 May 4;13(4):044107. doi: 10.1088/1748-605X/aab693.

Abstract

Electrospun fibrous scaffolds have been extensively used as cell-supporting matrices or delivery vehicles for various biomolecules in tissue engineering. Biodegradable scaffolds with tunable degradation behaviors are favorable for various resorbable tissue replacements. In nerve tissue engineering, delivery of growth factors (GFs) such as nerve growth factor (NGF) and glial cell line-derived neurotrophic factor (GDNF) from scaffolds can be used to promote peripheral nerve repair. In this study, using the established dual-source dual-power electrospinning technique, bicomponent scaffolds incorporated with NGF and GDNF were designed and demonstrated as a strategy to develop scaffolds providing dual GF delivery. NGF and GDNF were encapsulated in poly(D, L-lactic acid) (PDLLA) and poly(lactic-co-glycolic acid) (PLGA) nanofibers, respectively, via emulsion electrospinning. Bicomponent scaffolds with various mass ratios of GDNF/PLGA fibers to NGF/PDLLA fibers were fabricated. Their morphology, structure, properties, and the in vitro degradation were examined. Both types of core-shell structured fibers were evenly distributed in bicomponent scaffolds. Robust scaffolds with varying component ratios were fabricated with average fiber diameter ranging from 307 ± 100 nm to 688 ± 129 nm. The ultimate tensile stress and elastic modulus could be tuned ranging from 0.23 ± 0.07 MPa to 1.41 ± 0.23 MPa, 11.1 ± 3.0 MPa to 75.9 ± 3.3 MPa, respectively. Adjustable degradation was achieved and the weight loss of scaffolds ranged from 9.2% to 44.0% after 42 day degradation test. GDNF and NGF were incorporated with satisfactory encapsulation efficiency and their bioactivity were well preserved. Sustained release of both types of GFs was also achieved.

摘要

静电纺丝纤维支架已广泛用作细胞支持基质或用于组织工程中各种生物分子的传递载体。具有可调节降解行为的可生物降解支架有利于各种可吸收组织替代物。在神经组织工程中,支架中生长因子(GFs)的传递,如神经生长因子(NGF)和胶质细胞源性神经营养因子(GDNF),可用于促进周围神经修复。在这项研究中,使用已建立的双源双功率静电纺丝技术,设计并展示了包含 NGF 和 GDNF 的双组分支架,作为提供双重 GF 传递的策略。NGF 和 GDNF 通过乳液静电纺丝分别包封在聚(D,L-乳酸)(PDLLA)和聚(乳酸-共-羟基乙酸)(PLGA)纳米纤维中。制备了具有不同 GDNF/PLGA 纤维与 NGF/PDLLA 纤维质量比的双组分支架。对其形态、结构、性能和体外降解进行了研究。两种类型的核壳结构纤维在双组分支架中均匀分布。通过改变各组分的比例,制备了具有不同形貌的支架,平均纤维直径范围为 307±100nm 至 688±129nm。支架的拉伸强度和弹性模量可在 0.23±0.07MPa 至 1.41±0.23MPa,11.1±3.0MPa 至 75.9±3.3MPa 范围内进行调节。实现了可调节的降解,支架在 42 天降解测试后的失重率范围为 9.2%至 44.0%。NGF 和 NGF 的包封效率较高,生物活性保持良好。两种类型的 GF 都实现了持续释放。

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