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Growth behavior of endothelial cells according to electrospun poly(DL-lactic-co-glycolic acid) fiber diameter as a tissue engineering scaffold

机译:根据电纺聚(DL-乳酸-乙醇酸)纤维直径的内皮细胞的生长行为作为组织工程支架

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摘要

Investigating the effect of electrospun fiber diameter on endothelial cell proliferation provides an important guidance for the design of a fabric scaffold. In this study, we prepared biodegradable poly(D,L-lactic-co-glycolic acid) (PLGA) fibrous nonwoven mats with different fiber diameters ranged from 200 nm to 5 µm using the electrospinning technique. To control the fiber diameters of PLGA mats, 4 mixture solvents [hexafluoro-2-propanol, 2,2,2,-trifluoroethanol:dimethylformamide (9:1), 2,2,2,-trifluoroethanol:hexafluoro-2-propanol (9:1), chloroform] were used. Average diameters were 200 nm, 600 nm, 1.5 µm, and 5.0 µm, respectively. Stereoscopic structure and spatial characterization of fibrous PLGA mats were analyzed using atomic force microscopy and a porosimeter. The mechanical properties of PLGA mats were analyzed using a universal testing machine. The spreading behavior and infiltration of endothelial cells on PLGA mats were visualized by field emission scanning electron microscopy and hematoxylin and eosin staining. Cell proliferation on different PLGA fibers with different diameters was quantified using the MTT assay. Cells on 200 nm diameter PLGA mats showed rapid attachment and spreading. However, the cells did not penetrate the PLGA mat. Cells cultured on 600 nm and 1.5 µm diameter fibers could infiltrate the pores and cell proliferation was dramatically increased after 14 days. Secreted prostacyclin from endothelial cells on each mat was measured to examine the ability to inhibit platelet activation. This basic study on cell proliferation and fiber diameter with physical characterization provides a foundation for studies examining nonwoven fibrous PLGA mats as a tissue engineering scaffold.
机译:研究电纺纤维直径对内皮细胞增殖的影响为织物支架的设计提供了重要指导。在这项研究中,我们使用静电纺丝技术制备了可生物降解的聚(D,L-乳酸-乙醇酸)(PLGA)纤维非织造垫,其纤维直径从200 nm到5 µm不等。为了控制PLGA垫的纤维直径,需要使用4种混合溶剂[六氟-2-丙醇,2,2,2,-三氟乙醇:二甲基甲酰胺(9:1),2,2,2,-三氟乙醇:六氟-2-丙醇( 9:1),使用氯仿]。平均直径分别为200nm,600nm,1.5μm和5.0μm。使用原子力显微镜和孔隙率计分析纤维PLGA垫的立体结构和空间特征。使用通用测试机分析PLGA垫的机械性能。通过场发射扫描电子显微镜以及苏木精和曙红染色,可以观察到内皮细胞在PLGA垫上的扩散行为和浸润。使用MTT分析定量在具有不同直径的不同PLGA纤维上的细胞增殖。直径为200 nm的PLGA垫上的细胞显示出快速附着和扩散。但是,细胞没有穿透PLGA垫。在直径为600 nm和1.5 µm的纤维上培养的细胞可以渗入毛孔,并且在14天后细胞增殖急剧增加。测量每个垫上的内皮细胞分泌的前列环素,以检查抑制血小板活化的能力。这项具有物理特性的细胞增殖和纤维直径的基础研究为研究非织造纤维PLGA毡作为组织工程支架提供了基础。

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