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Multiple responses optimization in the development of a headspace gas chromatography method for the determination of residual solvents in pharmaceuticals

机译:顶空气相色谱法开发中用于测定药物中残留溶剂的多重响应优化

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摘要

An efficient generic static headspace gas chromatography (HSGC) method was developed, optimized and validated for the routine determination of several residual solvents (RS) in drug substance, using a strategy with two sets of calibration. Dimethylsulfoxide (DMSO) was selected as the sample diluent and internal standards were used to minimize signal variations due to the preparative step. A gas chroma-tograph from Agilent Model 6890 equipped with flame ionization detector (FID) and a DB-624 (30 m × 0.53 mm i.d., 3.00μm film thickness) column was used. The inlet split ratio was 5:1. The influ-encing factors in the chromatographic separation of the analytes were determined through a fractional factorial experimental design. Significant variables: the initial temperature (IT), the final temperature (FT) of the oven and the carrier gas flow rate (F) were optimized using a central composite design. Response transformation and desirability function were applied to find out the optimal combination of the chromatographic variables to achieve an adequate resolution of the analytes and short analysis time. These conditions were 30 °C for IT, 158 °C for FT and 1.90 mL/min for F. The method was proven to be accurate, linear in a wide range and very sensitive for the analyzed solvents through a comprehensive validation according to the ICH guidelines.
机译:使用具有两组校准的策略,开发,优化和验证了高效的通用静态通顶空气色谱(HSGC)方法,针对药物物质的几种残留溶剂(RS)进行了优化和验证。选择二甲基磺砜(DMSO),因为样品稀释剂和内标以最小化由于制备步骤而最小化信号变化。使用具有火焰电离检测器(FID)和DB-624(30m×0.53mm I.d.,3.00μm膜厚度)柱的Agilent Model 6890的气体色度谱图。入口分流比为5:1。通过分数阶乘实验设计确定分析物的色谱分离中的冲击因子。使用中央复合设计优化了显着变量:初始温度(IT),烘箱的最终温度(FT)和载气流速(F)进行了优化。应用响应变换和期望功能,以找出色谱变量的最佳组合,以实现分析物的足够分辨率和短分析时间。这些条件为30℃,FT为158℃,FT为1.90ml / min。该方法被证明是准确的,在宽范围内,通过根据ICH的全面验证,对分析的溶剂非常敏感指导方针。

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  • 来源
    《药物分析学报(英文)》 |2015年第005期|296-306|共11页
  • 作者单位

    Laboratorio de Control de Calidad de Medicamentos, Facultad de Bioquímica y Ciencias Biológicas, Universidad Nacional del Litoral, C.C.242, S3000ZAA Santa Fe, Argentina;

    Laboratorio de Control de Calidad de Medicamentos, Facultad de Bioquímica y Ciencias Biológicas, Universidad Nacional del Litoral, C.C.242, S3000ZAA Santa Fe, Argentina;

    Laboratorio de Control de Calidad de Medicamentos, Facultad de Bioquímica y Ciencias Biológicas, Universidad Nacional del Litoral, C.C.242, S3000ZAA Santa Fe, Argentina;

    Laboratorio de Control de Calidad de Medicamentos, Facultad de Bioquímica y Ciencias Biológicas, Universidad Nacional del Litoral, C.C.242, S3000ZAA Santa Fe, Argentina;

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  • 入库时间 2022-08-19 03:45:46
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