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Cell trauma detection using infra-red live cell imaging

机译:使用红外线活细胞成像进行细胞创伤检测

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Infra-red (IR) spectroscopic imaging of live cells is greatly affected by the presence of water, which is a strong absorber of IR radiation. In order to overcome this, a variety of methods have been developed using complex microfluidic devices to reduce the liquid sample path length. However, these devices are often custom made needing both specialised equipment and detailed fabrication steps. Here we show the novel utilisation of a liquid-air interface configuration and a negative contrast imaging device (NCI) reflectance imaging system for the collection of spectral data from live cells within an in vitro environment. Spectral differences were observed between two different cell densities, both in the presence and absence of cell culture media. Additionally, differences were observed between control and test cultures exposed to dimethyl sulfoxide (DMSO) to induce cell apoptosis. The NCI system acquired data in the 2.5 - 3.5 μm spectral region, at a spectral sampling interval of 10 nm. This method will allow further investigation of spectral bio-markers within cell cultures to augment understanding of specific cell contributions to wound healing in vivo.
机译:通过水存在,活细胞的红外线(IR)光谱成像受到水的存在,这是IR辐射的强吸收器。为了克服这一点,使用复杂的微流体装置开发了各种方法,以减少液体样品路径长度。然而,这些设备通常是定制的,需要专业设备和详细的制造步骤。在这里,我们示出了用于液体 - 空气接口配置的新颖利用和负对比度成像装置(NCI)反射成像系统,用于从体外环境内的活细胞集合的谱数据。在两种不同的细胞密度之间观察到光谱差异,在细胞培养基的存在和不存在中。另外,在暴露于二甲基亚甲醚(DMSO)的对照和测试培养物之间观察到差异以诱导细胞凋亡。 NCI系统以10nm的光谱采样间隔在2.5 - 3.5μm光谱区域中获取数据。该方法将允许进一​​步研究细胞培养物中的光谱生物标记,以增加对体内伤口愈合的特定细胞贡献的认识。

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