Identification of Two Novel Hydroperoxide Impurities in Fluocinolone Acetonide Topical Solution by Liquid Chromatography Mass Spectrometry.

IF 1.5 4区 化学 Q4 BIOCHEMICAL RESEARCH METHODS Journal of chromatographic science Pub Date : 2024-05-31 DOI:10.1093/chromsci/bmad003
DasameswaraRao Kavitapu, Nagadeep Jaishetty, Arthanareeswari Maruthapillai, J N S R C Murty
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Abstract

Fluocinolone acetonide topical is used to treat skin discomforts such as swelling, itching and redness by activating the natural substances in the skin. Several process-related impurities and degradation products are identified and reported. But hydroperoxide impurities in Fluocinolone acetonide topical solution are not reported anywhere. In this study, we identify two potential genotoxic isomeric hydroperoxide impurities in Fluocinolone acetonide topical solution by Liquid Chromatography Mass Spectrometry analysis. A possible mechanism for the formation of these two novel hydroperoxide impurities is based on the neighboring group participation effect of adjacent hydroxyl group (Internal SN2) which results in the loss of fluorine atom and formation of epoxide intermediate followed by the addition of the HOOH group. Since most of the hydroperoxide impurities are genotoxic in nature, one should eliminate these impurities from Active Pharmaceutical Ingredient (API) or protect the formulation product from these oxidative impurities.

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利用液相色谱质谱法鉴定阿塞通氨氟西酮外用溶液中的两种新型过氧化氢杂质
外用氟西诺龙通过激活皮肤中的天然物质来治疗皮肤不适,如红肿、瘙痒和发红。已发现并报告了几种与加工过程有关的杂质和降解产物。但是氟西诺龙醋酸肤轻松外用溶液中的过氧化氢杂质却没有任何报道。在本研究中,我们通过液相色谱-质谱分析法确定了氟西酮缩丙酮外用溶液中两种潜在的基因毒性异构体过氧化氢杂质。这两种新型过氧化氢杂质的可能形成机制是基于相邻羟基的邻位基团参与效应(内部 SN2),该效应导致氟原子丢失,形成环氧化物中间体,然后再加入 HOOH 基团。由于大多数过氧化氢杂质都具有基因毒性,因此应从活性药物成分(API)中去除这些杂质,或保护制剂产品免受这些氧化杂质的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.90
自引率
7.70%
发文量
94
审稿时长
5.6 months
期刊介绍: The Journal of Chromatographic Science is devoted to the dissemination of information concerning all methods of chromatographic analysis. The standard manuscript is a description of recent original research that covers any or all phases of a specific separation problem, principle, or method. Manuscripts which have a high degree of novelty and fundamental significance to the field of separation science are particularly encouraged. It is expected the authors will clearly state in the Introduction how their method compares in some markedly new and improved way to previous published related methods. Analytical performance characteristics of new methods including sensitivity, tested limits of detection or quantification, accuracy, precision, and specificity should be provided. Manuscripts which describe a straightforward extension of a known analytical method or an application to a previously analyzed and/or uncomplicated sample matrix will not normally be reviewed favorably. Manuscripts in which mass spectrometry is the dominant analytical method and chromatography is of marked secondary importance may be declined.
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