稳定性指示方法用于氯唑唑酮中潜在的遗传毒性杂质和其他有机杂质的定量

IF 1.3 Q4 CHEMISTRY, ANALYTICAL SEPARATION SCIENCE PLUS Pub Date : 2023-11-02 DOI:10.1002/sscp.202300138
Bhujanga Rao Nagulancha, Vandavasi Koteswara Rao
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引用次数: 0

摘要

摘要:建立了一种简便、可靠、稳定的RP - HPLC - UV测定骨骼肌松弛剂氯唑唑酮中相关物质(对氯酚和未知杂质)的方法,并进行了验证。此外,由于该化合物含有潜在的遗传毒性杂质(2‐氨基‐4‐氯苯酚),需要在定量时具有更高的灵敏度,我们还开发并验证了一种单独的RP - HPLC -质谱(MS)/MS方法,用于估计2‐氨基‐4‐氯苯酚杂质。两种方法(RP - HPLC - UV;RP - HPLC - MS/MS)根据国际统一委员会Q2(R1)进行了验证,发现其精确、准确、稳健、线性和特异性,其定量限为100%的测试浓度,RP - HPLC - UV为0.018% w/w的对氯酚,RP - HPLC - MS为2ppm的2 -氨基- 4 -氯酚。
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Stability‐indicating method for quantification of potential genotoxic impurity and other organic impurities of chlorzoxazone using hyphenated techniques
Abstract A simple, reliable, and stability‐indicating RP‐HPLC‐UV method was developed and validated for the estimation of related substances ( p ‐chlorophenol and unknown impurities) of chlorzoxazone (skeletal muscle relaxant). Along with this as the compound contains a potential genotoxic impurity (2‐amino‐4‐chlorophenol), which needs to have more sensitivity in quantification, we have also developed and validated a separate RP‐HPLC‐mass spectrometry (MS)/MS method for the estimation of 2‐amino‐4‐chlorophenol impurity. Both methods (RP‐HPLC‐UV & RP‐HPLC–MS/MS) were validated in accordance with International Council for Harmonization Q2(R1) and were found to be precise, accurate, robust, linear, and specific with limit of quantification values established with respect to 100% of test concentration, 0.018% w/w of p ‐chlorophenol by RP‐HPLC‐UV, and 2 ppm of 2‐amino‐4‐chlorophenol by RP‐HPLC–MS.
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来源期刊
SEPARATION SCIENCE PLUS
SEPARATION SCIENCE PLUS CHEMISTRY, ANALYTICAL-
CiteScore
1.90
自引率
9.10%
发文量
111
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