A Novel Validated HS-GC-MS method for the Trace Level Determination of Acetyl Chloride as Isopropyl Acetate in Various Anti-cancer Drug Substances

Srivalli Kasina, Annapurna Nowduri, R. Chavakula
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Abstract

A novel, simple and precise headspace gas chromatography-mass spectrometry (HS-GC-MS) method was developed and validated for the determination of acetyl chloride (AC) in various anti-cancer drug substances like bendamustine HCl, Ibrutinib, trifluridine and abemaciclib drug substances. In this methodology, AC reacts with isopropyl alcohol and is converted into isopropyl acetate. Hence AC is quantified as Isopropyl acetate. The lower level of detection was achieved on the capillary GC column (DB-624, Fused silica capillary column; 30 m length; 0.32 mm internal diameter, coated with 6% Cyanopropylphenyl and 94% dimethyl polysiloxane stationary phase of 1.8 μm film thickness) with electron impact ionization (EI) technique by GC-MS in selective ion monitoring (SIM) mode. The mass ions were selected for the quantifier is 63 and the qualifier is 87 for isopropyl acetate. The performance of the method was assessed by evaluating the specificity, linearity, sensitivity, precision, accuracy and robustness experiments. The established limit of detection and limit of quantification values for the AC were 0.1 and 0.3 μg/g, respectively. This developed method was found to be linear with a correlation coefficient is greater than 0.999 for all four drug substances. The average recoveries of AC in bendamustine HCl, ibrutinib, trifluridine and abemaciclib were obtained 106.1, 109.0, 97.4 and 101.6%, respectively. The proposed method was validated successfully as per ICH guidelines. Hence, the proposed method can be routinely used for the quantification of AC in various anti-cancer drug substances.
用于痕量测定各种抗癌药物中作为乙酸异丙酯的乙酰氯的新型验证 HS-GC-MS 方法
本研究开发并验证了一种新颖、简便、精确的顶空气相色谱-质谱(HS-GC-MS)方法,用于测定多种抗癌药物(如盐酸苯达莫司汀、伊布替尼、曲夫鲁啶和阿贝替尼)中的乙酰氯(AC)。在此方法中,乙酰氯与异丙醇反应,转化为乙酸异丙酯。因此,AC 被定量为乙酸异丙酯。毛细管气相色谱柱(DB-624,熔融石英毛细管柱;长 30 米;内径 0.32 毫米,涂有 6% 氰丙基苯基和 94% 二甲基聚硅氧烷固定相,膜厚 1.8 μm)采用电子碰撞电离(EI)技术,气相色谱-质谱仪(GC-MS)在选择离子监测(SIM)模式下实现了较低的检测水平。乙酸异丙酯的定量离子为 63,定性离子为 87。通过特异性、线性、灵敏度、精密度、准确度和稳健性实验对该方法的性能进行了评估。乙酸异丙酯的检出限和定量限分别为 0.1 和 0.3 μg/g。该方法线性关系良好,四种药物的相关系数均大于 0.999。苯达莫司汀盐酸盐、伊布替尼、曲夫卢啶和阿贝西利中AC的平均回收率分别为106.1%、109.0%、97.4%和101.6%。根据 ICH 指南,所提议的方法成功通过了验证。因此,该方法可用于各种抗癌药物中AC的常规定量分析。
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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