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In?situ observation of a cell adhesion and metabolism using surface infrared spectroscopy

机译:使用表面红外光谱原位观察细胞粘附和代谢

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摘要

In this study, we report on an in?situ monitoring system of living cultured cells using infrared absorption spectroscopy in the geometry of multiple internal reflections (MIR-IRAS). In order to observe living cultured cells, the temperature in the sample chamber of a FT-IR spectrometer was maintained at 37?°C and a humidified gas mixture containing 5% CO2 was introduced into the sample chamber. Human breast cell line MCF-7 cultured on Si MIR prisms were placed in the sample chamber and infrared spectra of MCF-7 cells were collected for 5?h. It was found that the adhesion and metabolism of MCF-7 cells could be monitored by the absorption intensity of amide-II protein band (1,545?cm?1) and also by the absorption intensities of CHx bands (2,700–3,100?cm?1). These results suggest that our system is useful for a nondestructive and non-label monitoring of cell viability. Our method based on infrared absorption spectroscopy has a potential for bioscreening application.
机译:在这项研究中,我们报告了在多个内部反射(MIR-IRAS)的几何形状中使用红外吸收光谱对活培养细胞的原位监测系统。为了观察活的培养细胞,将FT-IR光谱仪的样品室中的温度保持在37℃,并且将含有5%CO 2的加湿气体混合物引入样品室中。将在Si MIR棱镜上培养的人乳腺细胞系MCF-7放置在样品室中,并收集MCF-7细胞的红外光谱达5?h。结果发现,MCF-7细胞的粘附和代谢可以通过酰胺II蛋白带的吸收强度(1,545?cm?1)和通过CHx谱带的吸收强度(2,700–3,100?cm?1)来监测。 )。这些结果表明我们的系统可用于细胞活力的非破坏性和非标记性监测。我们基于红外吸收光谱法的方法具有生物筛选应用的潜力。

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