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摘要:
With the ever increasing complexity of active pharmaceutical ingredient (API) preparations, more potential genotoxic impurities (PGI’s) are being observed. It is thus necessary to determine if these PGI’s are present in the final API’s, and if they are present, to ensure the levels are acceptable for any clinical uses. For PGI’s that have authentic standards available, quantitation can be accomplished in a straightforward manner. However, for PGI’s that are expected to form through rearrangements or side reactions, authentic standards may not be readily available, significantly complicating the analysis. In this study we describe a surrogate standard approach for quantifying PGI’s that allows for relative response factor calculations of PGI species utilizing both gas chromatography-mass spectrometry (GC-MS) and liquid chromatography-mass spectrometry (LC-MS).
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篇名 Quantitation of Genetox Impurities Using a Surrogate Standard Approach
来源期刊 分析科学方法和仪器期刊(英文) 学科 医学
关键词 Potential GENOTOXIC Impurity (PGI) Active Pharmaceutical INGREDIENT (API) Mass Spectrometry Surrogate STANDARD ANALYTE Relative Response Factor (RRF)
年,卷(期) fxkxffhyqqkyw_2013,(3) 所属期刊栏目
研究方向 页码范围 167-172
页数 6页 分类号 R73
字数 语种
DOI
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研究主题发展历程
节点文献
Potential
GENOTOXIC
Impurity
(PGI)
Active
Pharmaceutical
INGREDIENT
(API)
Mass
Spectrometry
Surrogate
STANDARD
ANALYTE
Relative
Response
Factor
(RRF)
研究起点
研究来源
研究分支
研究去脉
引文网络交叉学科
相关学者/机构
期刊影响力
分析科学方法和仪器期刊(英文)
季刊
2164-2745
武汉市江夏区汤逊湖北路38号光谷总部空间
出版文献量(篇)
125
总下载数(次)
0
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