测定多种药物中 I 类残留溶剂的顶空气相色谱质谱法:通过设计质量统计工具进行方法评估。

Kousrali Sayyad, Leela Prasad Kowtharapu, Tanmoy Mondal
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引用次数: 0

摘要

背景:1,1-二氯乙烷、1,1,1-三氯乙烷、四氯化碳、苯、1,2-二氯乙烷等一类残留溶剂具有毒性,对环境有害,对人体致癌。顶空气相色谱质谱仪是对残留溶剂进行下限定量的精密仪器:利用顶空气相色谱质谱仪,建立了一种准确、灵敏、可靠和快速的方法来测定不同药物中的 1,1-二氯乙烷、1,1,1-三氯乙烷、四氯化碳、苯和 1,2-二氯乙烷:方法:该方法使用氦气作为载气。方法:以氦气为载气,N-甲基-2-吡咯烷酮为稀释剂,DB-624(60 m x 0.25 mm x 1.4 μm膜厚)色谱柱为固定相,流速为 1.5 mL/min:结果:1,1-二氯乙烷、1,1,1-三氯乙烷、四氯化碳、苯和 1,2-二氯乙烷的检测限浓度分别为 0.24 ppm、5 ppm、0.12 ppm、0.06 ppm 和 0.15 ppm。随后,上述杂质的定量限浓度分别为 0.8 ppm、15 ppm、0.4 ppm、0.2 ppm 和 0.5 ppm。线性范围为 LOQ 至 120%:结论:当前方法的系统适用性、精密度、线性度和准确度参数符合美国药典和 ICH Q2(R2),结果在接受标准范围内:关于盐酸林可霉素、达帕利嗪、富马酸冯诺普拉嗪、替米沙坦等药物中一类残留溶剂的测定,目前尚无相关研究报道。拟议的研究旨在开发药物物质 I 类残留溶剂定量的通用方法。在方法性能验证中采用了 QbD 概念。
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Headspace Gas Chromatography-Mass Spectrometry Method for Determination of Class-I Residual Solvents in Several Drug Substances: Method Evaluation by Quality by Design Statistical Tool.

Background: Class-I residual solvents such as 1,1-dichloroethene, 1,1,1-trichloroethane, carbon tetrachloride, benzene, 1,2-dichloroethane are toxic, environmental hazards, and carcinogenic to humans. A headspace-gas chromatography-mass spectrometer is a sophisticated instrument for the quantification of residual solvents at lower limits.

Objective: An exact, sensitive, reliable, and fast method was developed to determine 1,1-dichloroethene, 1,1,1-trichloroethane, carbon tetrachloride, benzene, and 1,2-dichloroethane present in different drug substances using a headspace-gas chromatography-mass spectrometer.

Methods: Helium is used as a carrier gas. N-methyl-2-pyrrolidone is used as a diluent, and the stationary phase is a DB-624 (60 m × 0.25 mm × 1.4 μm film thickness) column with a flow rate of 1.5 mL/min.

Results: The concentration LODs for 1,1-dichloroethene, 1,1,1-trichloroethane, carbon tetrachloride, benzene, and 1,2-dichloroethane were 0.24, 5, 0.12, 0.06, and 0.15 ppm. The concentrations LOQs for the aforementioned impurities were 0.8, 15, 0.4, 0.2, and 0.5 ppm. The linearity was assessed over the range from LOQ to 120% of the specification level.

Conclusion: The current method's system suitability, precision, linearity, and accuracy parameters were assessed in accordance with the United states pharmacopeia (USP) < 1225> and International Conference on Harmonization of technical standards for the registration of medicines for human use (ICH) Q2(R2), and the results were within the acceptance criteria.

Highlights: No research studies have been reported on determining class-I residual solvents in lincomycin hydrochloride, dapagliflozin, vonoprazan fumarate, and telmisartan drug substances. The proposed research aims to develop a common method for the quantification of class-I residual solvents for drug substances. The quality by design (QbD) concept is utilized in performance verification.

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