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首页> 外文期刊>Biotechnology Progress >Quantitation and Characterization of Process Impurities and Extractables in Protein-Containing Solutions Using Proton NMR as a General Tool
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Quantitation and Characterization of Process Impurities and Extractables in Protein-Containing Solutions Using Proton NMR as a General Tool

机译:使用质子NMR作为通用工具对蛋白质溶液中的过程杂质和可萃取物进行定量和表征

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摘要

The ability to detect and quantitate a variety of components in solution has become increasingly important in carrying out efficient and rigorous validation studies for biophar-maceutical manufacturing processes. Here, we demonstrate the general applicability of NMR spectroscopy for the identification and quantitation of leachables and other impurities in protein-based drugs, at low levels previously unattainable in protein-containing solutions. With improved NMR technology (i.e., CryoProbes) and the application of a Carr-Purcell-Mei-boom-Gill pulse sequence (CPMG) to attenuate protein signals, we have been able to use NMR to quantify impurities in a protein-based biopharmaceutical product at ~1 μg mL~(-1). The data indicate that NMR spectra can be used to quantitate a range of impurities, from small molecule components to higher molecular weight leachables, without removing protein from solution. Furthermore, quantitation of impurities by NMR is reliable and accurate enough for biopharmaceutical process validation, even for high molecular weight extractables whose structures are not precisely known.
机译:检测和定量解决方案中各种成分的能力在进行有效且严格的生物相-制造过程验证研究中变得越来越重要。在这里,我们证明了NMR光谱的普遍适用性,用于鉴定和定量蛋白质基药物中的可浸出物和其他杂质,含量低,以前是含蛋白质溶液中无法达到的。通过改进的NMR技术(例如CryoProbes)和Carr-Purcell-Mei-Boom-Gill脉冲序列(CPMG)的应用来衰减蛋白质信号,我们已经能够使用NMR定量基于蛋白质的生物制药产品中的杂质在〜1μgmL〜(-1)。数据表明,NMR光谱可用于定量从小分子组分到更高分子量可浸出物的一系列杂质,而无需从溶液中去除蛋白质。此外,即使对于结构未知的高分子量可萃取物,通过NMR进行杂质定量也足够可靠和准确,可用于生物制药过程验证。

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