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Monitoring of heat- and light exposure of cell culture media by RAMAN spectroscopy: Towards an analytical tool for cell culture media quality control

机译:拉曼光谱法监测细胞培养基的热敏和曝光:朝向细胞培养基质量控制的分析工具

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摘要

Cell culture media are highly complex solutions of multiple nutrients for mammalian cells and lay the foundation for enhanced quality of the expressed protein and the performance of the bioprocess. Especially for long term, large-volume continuous production processes the constant quality of media without compositional variation is desirable, despite exposure to various stress conditions like (UV)-light or (high)-temperature cannot be represented by a measurable parameter yet. In this study, chemometric analysis of non-enhanced RAMAN spectra was used to identify different cell culture media and to track accelerated degradation conditions by light or temperature in aqueous solutions of glucose and chemically defined media. To link the changes in the RAMAN spectra with cell culture parameters we used the untreated and stressed media for biophysical and biochemical measurements as well as cell culture experiments. The two tested media were exceptionally stable against heat, but showed diminished biological performance after light exposure accompanied by reduced concentrations of the key amino acids Met, His, Trp and Lys. RAMAN spectroscopy provides a rapid and non-destructive method to distinguish individual cell culture media and to find even minor differences between otherwise comparable media lots. In this study we demonstrate the suitability of RAMAN spectroscopy for identity- and quality testing of various process media as an exciting tool for implementation in quality control of bioprocessing.
机译:细胞培养基是哺乳动物细胞的多种营养素的高度复杂溶液,并为表达蛋白质的增强质量和生物过程的性能奠定基础。特别是对于长期来说,大容量连续生产过程不需要组成变化的常量介质质量,尽管暴露于诸如(UV) - 灯或(高) - 尚不通过可测量的参数表示的各种应力条件。在该研究中,使用非增强拉曼光谱的化学计量分析来鉴定不同的细胞培养基,并通过葡萄糖和化学限定的培养基的水溶液中的光或温度跟踪加速降解条件。为了将拉曼光谱的变化与细胞培养参数联系在细胞培养参数中,我们使用未处理和强调的培养基,用于生物物理和生化测量以及细胞培养实验。两种测试的介质对热量稳定,但在伴随着浓度的关键氨基酸,他,TRP和Lys的浓度降低后,伴随着浓度的生物学性能减少。拉曼光谱提供了一种快速和非破坏性的方法来区分单个细胞培养基并在其他媒体批次之间找到甚至在其他媒体之间的微小差异。在这项研究中,我们证明了拉曼光谱对各种过程介质的身份和质量测试的适用性,作为生物处理质量控制的令人兴奋的工具。

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