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Deep-Ultraviolet Resonance Raman (DUVRR) Spectroscopy of Therapeutic Monoclonal Antibodies Subjected to Thermal Stress

机译:承受热应激的治疗性单克隆抗体的深紫外共振拉曼光谱(DUVRR)

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摘要

The structural assessment of Rituximab, an IgG1 mAb, was investigated with deep-ultraviolet resonance Raman (DUVRR) spectroscopy. DUVRR spectroscopy was used to monitor the changes to the secondary structure of Rituximab under thermal stress. DUVRR spectra showed obvious changes from 22 to 72 degrees C. Specifically, changes in the amide I vibrational mode were assigned to an increase in unordered structure (random coil). Structural changes in samples heated to 72 degrees C were related to loss in drug potency via a complement dependent cytotoxicity (CDC) bioassay. The DUVRR spectroscopic method shows promise as a tool for the quality assessment of mAb drug products and would represent an improvement over current methodology in terms of analysis time and sample preparation. To determine the scope of the method, protein pharmaceuticals of different molecular weights (ranging from 4 to 143 kDa) and secondary structure (beta-sheet, alpha-helix and unordered structure) were analyzed. The model illustrated the methods sensitivity for the analysis of protein drug products of different secondary structure. Results show promise for DUVRR spectroscopy as a rapid screening tool of a variety of formulated protein pharmaceuticals.
机译:用深紫外共振拉曼光谱(DUVRR)对利妥昔单抗(一种IgG1 mAb)的结构进行了评估。 DUVRR光谱用于监测热应激下利妥昔单抗二级结构的变化。 DUVRR光谱显示出从22摄氏度到72摄氏度的明显变化。具体地说,酰胺I振动模式的变化被归因于无序结构(无规卷曲)的增加。通过补体依赖性细胞毒性(CDC)生物测定,加热至72摄氏度的样品的结构变化与药物效能的下降有关。 DUVRR光谱方法显示出有望作为mAb药物产品质量评估的工具,并且在分析时间和样品制备方面将代表对当前方法的一种改进。为了确定该方法的范围,分析了不同分子量(范围从4至143 kDa)和二级结构(β-折叠,α-螺旋和无序结构)的蛋白质药物。该模型说明了分析不同二级结构蛋白质药物产品的方法灵敏度。结果表明,DUVRR光谱技术有望作为多种配制蛋白药物的快速筛选工具。

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