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首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Establishment of a reference standard database for use in the qualitative and semi-quantitative analysis of pharmaceutical contact materials within an extractables survey by GC-MS
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Establishment of a reference standard database for use in the qualitative and semi-quantitative analysis of pharmaceutical contact materials within an extractables survey by GC-MS

机译:建立参考标准数据库,用于使用GC-MS的提取物调查中的药物接触材料的定性和半定量分析

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摘要

The analysis of reference standards may be performed to enhance the qualitative and quantitative data generated by non-specific screening methods utilized in extractables studies performed on pharmaceutical contact materials. However, the establishment of a database containing relative response factor and retention index values obtained from these standards has not been published. In this study, the establishment of such a database for GC-MS, a methodology commonly included in extractables studies, on an intra-lab basis was investigated. A set of 154 organic compounds representing a diverse range of chemical functionalities and properties was analyzed at eight time points on four GC-MS instruments that represent the diversity of age and model at our laboratory. The results of this study have shown that any variance in relative response factor between instruments was not significant from a practical perspective as supported by the coefficient of variation values (n =32), which were = 15% and = 10% for 75% and 45% of the compounds tested, respectively. Furthermore, the retention index of the compounds, as expressed by retention time and relative retention time, did not have more than a 2% coefficient of variation between instruments or columns in most cases. It was concluded that a database of these values could be established for future use in extractables studies on an intra-laboratory basis. (C) 2017 Elsevier B.V. All rights reserved.
机译:可以进行参考标准的分析以增强通过在药物接触材料的提取物研究中使用的非特异性筛选方法产生的定性和定量数据。但是,尚未公布包含从这些标准获得的相对响应因子和从这些标准获得的保留指标值的数据库的建立。在本研究中,研究了对GC-MS的这种数据库的建立,一种常用于实验室内的提取物研究中的方法。在四个GC-MS仪器上以8个GC-MS仪器分析了代表各种化学功能和性质和性质的一组154种有机化合物,该仪器代表了我们实验室的年龄和模型的多样性。该研究的结果表明,由于仪器之间的相对响应因子之间的任何方差与由变异系数(n = 32)支撑的实际角度不显着,这是& = 15%,并且<= 10% 75%和45%的化合物分别测试。此外,在大多数情况下,通过保留时间和相对保留时间表达的化合物的保留指数在大多数情况下,仪器或柱之间的变异系数不超过2%。得出结论,可以建立这些价值的数据库,以便在实验室内的提取物研究中的萃取物研究中建立。 (c)2017年Elsevier B.V.保留所有权利。

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