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首页> 外文期刊>Vibrational Spectroscopy: An International Journal devoted to Applications of Infrared and Raman Spectroscopy >Preventing damage of germanium optical material in attenuated total reflection-Fourier transform infrared (ATR-FTIR) studies of living cells
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Preventing damage of germanium optical material in attenuated total reflection-Fourier transform infrared (ATR-FTIR) studies of living cells

机译:防止锗光学材料的损伤在减毒的总反射 - 傅里叶变换红外(ATR-FTIR)研究中的活细胞

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Germanium is an important element for ATR-FTIR spectroscopy. It has often been selected as a substrate for live cells FTIR spectroscopy because of its low toxicity for most human cells. However, there is a lack of study on the physical interactions between germanium and the living cells. In this study, we have shown that germanium surfaces are easily damaged when living cells are grown directly in contact for more than 20 h on the element surface. We then proposed a methodology to reduce the damage by coating the surface of the element with a thin layer of biological materials and tested for their capacities to protect polished germanium surfaces from living cell cultures. Fibronectin, collagen and gelatine coated and non-coated, newly polished Ge plates were subjected to 48 h culture of HeLa cells for six times and the degree of erosion by the cell was monitored using optical and atomic force microscopy (AFM). The cells showed normal attachment and morphology to either the treated or untreated surfaces and the viability of the cells were confirmed by trypan blue assay. Furthermore we have tested with an ATR FTIR measurement with a multi-bounce Ge element and found that the coatings were thin enough not to interfere with the measurements. However the degree of erosion (measured by the roughness of the Ge plate after cell culturing) was found to depend on the types of coating used where gelatine coating showed the best protection. (C) 2016 The Authors. Published by Elsevier B.V.
机译:锗是ATR-FTIR光谱的重要因素。由于其对大多数人细胞的低毒性,通常被选择为活细胞的底物。然而,缺乏研究锗和活细胞之间的物理相互作用。在这项研究中,我们已经表明,当活细胞直接在元件表面上达到20小时以上时,锗表面容易受损。然后,我们提出了一种方法,通过用薄的生物材料涂覆元件的表面来减少损伤,并测试它们的能力以保护抛光锗表面免受活细胞培养物。纤维蛋白,胶原蛋白和明胶涂覆和非涂覆的新抛光的GE板对Hela细胞的48小时培养六次,并且使用光学和原子力显微镜(AFM)监测细胞的腐蚀程度。细胞显示正常的附着和形态,对处理或未治疗的表面和细胞的可生存性通过台盼蓝测定确认。此外,我们用ATR FTIR测量用多次反弹GE元素进行了测试,发现涂层足够薄,不能干扰测量。然而,发现侵蚀程度(通过电池培养后Ge板的粗糙度测量)取决于使用明胶涂层显示最佳保护的涂层类型。 (c)2016年作者。 elsevier b.v出版。

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