A.C, Unidad de Materiales, Calle 43 No. 130, Centro de Investigación Científica de Yucatán, Col. Chuburná de Hidalgo, C.P. 97205, Mérida, Yucatán, México.
Facultad de Ingeniería Química, Periférico Norte Km 33.5 Tablaje Catastral 13615, Universidad Autónoma de Yucatán, Chuburná de Hidalgo Inn, C.P. 97203, Mérida, Yucatán, México.
J Mater Sci Mater Med. 2022 May 18;33(6):45. doi: 10.1007/s10856-022-06668-1.
The surface of Tecoflex SG-80A Polyurethane (PU) films was modified by grafting polyethylene glycol (PEG) chains at three different molar amounts (0.05, 0.10, and 0.15 mmol). The resulting substrata were characterized by FTIR-ATR, TGA, AFM, SEM and contact angle to assess the surface modifications occurred during the grafting reactions. Osteoblasts and fibroblasts were cultured with PU extracts for 24 h, and their cell viability and morphology were evaluated by CellTiterBlue assay, Crystal Violet staining and Live/Dead assay. FTIR and TGA results indicated that PEG chains were successfully grafted onto PU surfaces, specifically in the hard segment of PU forming allophanate groups as the PEG grafting density increased. SEM and AFM images suggest that PU substrata were partially covered by PEG, increasing the dispersive and basic components of the PU surface energy. It was found that extracts from PEG-grafted polyurethanes increased the osteoblast viability, although fibroblasts viability remained constant regardless PEG grafting density; in spite of this both cells presented a more spread morphology at the lower PEG grafting density. Our results showed that surface energy of PU substrata can be tuned by PEG grafting density; also, the PEG leached tends to increase the pH of culture medium which leads to a higher viability of osteoblasts; nevertheless, PEG grafting density should be optimized to promote a healthy cell morphology as alterations in its morphology were detected at higher concentrations. Graphical abstract.
Tecoflex SG-80A 型聚氨酯(PU)薄膜的表面通过接枝三种不同摩尔量(0.05、0.10 和 0.15 mmol)的聚乙二醇(PEG)链来进行改性。采用傅里叶变换衰减全反射红外光谱(FTIR-ATR)、热重分析(TGA)、原子力显微镜(AFM)、扫描电子显微镜(SEM)和接触角对所得基底进行了表征,以评估接枝反应过程中发生的表面改性。将成骨细胞和纤维母细胞与 PU 提取物共培养 24 h,通过 CellTiterBlue 检测、结晶紫染色和 Live/Dead 检测评估细胞活力和形态。FTIR 和 TGA 结果表明,PEG 链成功接枝到 PU 表面,特别是在 PU 的硬段中形成了三聚氰胺基团,PEG 接枝密度增加。SEM 和 AFM 图像表明,PEG 接枝后的 PU 基底部分被 PEG 覆盖,增加了 PU 表面能的色散和碱性成分。结果发现,PEG 接枝聚氨酯的提取物增加了成骨细胞的活力,尽管纤维母细胞的活力保持不变,与 PEG 接枝密度无关;尽管如此,两种细胞在较低的 PEG 接枝密度下呈现出更舒展的形态。我们的研究结果表明,PU 基底的表面能可以通过 PEG 接枝密度进行调节;此外,PEG 的浸出会增加培养基的 pH 值,从而提高成骨细胞的活力;然而,PEG 接枝密度应该进行优化,以促进细胞形态健康,因为在较高浓度下检测到细胞形态的改变。图表摘要。