单纯形搜索框架的构建,用于开发一种新的特异性和鲁棒性稳定性指示反相高效液相色谱法:用于肽基端粒酶疫苗的稳定性

IF 2.8 3区 工程技术 Q2 CHEMISTRY, ANALYTICAL
Claire Andre, Lydie Lethier, Yves Claude Guillaume
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引用次数: 0

摘要

在这项工作中,描述了一种新的数学算法,用于开发高效液相色谱(HPLC)稳定性指示分析。这种方法被应用于一种通用的癌症肽基端粒酶疫苗的稳定性研究,该疫苗由两种肽的混合物组成。采用计算机辅助设计的实验-单纯形算法软件,仅通过18个实验,确定了最佳的HPLC梯度条件。此外,还实现了异天冬氨酸肽降解产物与活性药物成分的色谱分离。该方法按照国际协调委员会的指导方针进行了验证。结果表明,该疫苗在- 20℃硼硅玻璃小瓶中保存2个月,物化性能稳定,未检测到异天冬氨酸肽的形成。此外,该疫苗在解冻样品后在4°C或室温下稳定达10小时。未观察到潜在温度漂移对硼硅玻璃小瓶中疫苗浓度的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Construction of a Simplex Search Framework for the Development of a New Specific and Robust Stability-Indicating Reversed-Phase High-Performance Liquid Chromatography Assay: Application for the Stability of a Peptide-Based Telomerase Vaccine

In this work, a novel mathematical algorithm was described for the development of a high-performance liquid chromatography (HPLC) stability-indicating assay. This approach was applied for the stability study of a universal cancer peptide-based telomerase vaccine constituted of a mixture of two peptides. With only 18 experiments, the optimum HPLC gradient conditions were determined using a computer-assisted design of experiments—simplex algorithm software. In addition, the separation on the chromatogram of the isoaspartate peptide degradation product with the active pharmaceutical ingredients was achieved. This HPLC method was validated as per the International Committee on Harmonization guidelines. It was shown that this vaccine was physicochemical stable for 2 months when stored in borosilicate glass vials at −20°C and no formation of isoaspartate peptide was detected. In addition, this vaccine was stable for up to 10 h at 4°C or room temperature after thawing the samples. No impact of potential temperature excursion on the vaccine concentration in the borosilicate glass vial was observed.

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来源期刊
Journal of separation science
Journal of separation science 化学-分析化学
CiteScore
6.30
自引率
16.10%
发文量
408
审稿时长
1.8 months
期刊介绍: The Journal of Separation Science (JSS) is the most comprehensive source in separation science, since it covers all areas of chromatographic and electrophoretic separation methods in theory and practice, both in the analytical and in the preparative mode, solid phase extraction, sample preparation, and related techniques. Manuscripts on methodological or instrumental developments, including detection aspects, in particular mass spectrometry, as well as on innovative applications will also be published. Manuscripts on hyphenation, automation, and miniaturization are particularly welcome. Pre- and post-separation facets of a total analysis may be covered as well as the underlying logic of the development or application of a method.
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