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Quality control in residual solvent analysis: the static headspace gas chromatographic method

机译:残留溶剂分析中的质量控制:静态顶空气相色谱法

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Residual solvent testing of raw materials and drug products constitutes part of a quality control programme. Static headspace gas chromatography (HS/GC) is suggested in current pharmacopoeias as a general tool for residual solvent testing. But the main obstacles to using HS/GC procedures are the absence of performance tests, suitable reference solvents and matrix standards, and reference methods. Harmonized regulations for residual solvent testing allow the use of a cumulative approach to estimate the residual solvent content in drug products. The supplier data may be appropriate. Therefore, in a quality control programme the main accent is put on the definition of specification limits (in accordance with toxicological data, and the influence of residual solvents on the physical properties and stability of the product) and supplier qualification. This paper focuses on two main problems linked to supplier qualification: system performance and matrix effect. HS/GC of a mixture containing solvents of different volatility and polarity is proposed as a performance test. The test can be done in three ways in accordance with the residual solvents characteristics, the test sample solubility and the specification levels required. The use of the test as a diagnostic tool is demonstrated and sources of uncertainty of the recovery determination are discussed. [References: 8]
机译:原料和药品的残留溶剂测试是质量控制计划的一部分。在目前的药典中建议使用静态顶空气相色谱法(HS / GC)作为残留溶剂测试的通用工具。但是,使用HS / GC程序的主要障碍是缺乏性能测试,合适的参比溶剂和基质标准品以及参比方法。残留溶剂测试的统一法规允许使用累积方法来估计药品中的残留溶剂含量。供应商数据可能是适当的。因此,在质量控制程序中,主要重点是规格限制的定义(根据毒理学数据以及残留溶剂对产品物理性能和稳定性的影响)和供应商资格。本文关注与供应商资格相关的两个主要问题:系统性能和矩阵效应。提议将含有挥发性和极性不同的溶剂的混合物的HS / GC作为性能测试。根据残留溶剂的特性,测试样品的溶解度和所需的规格水平,可以通过三种方式进行测试。证明了该测试方法作为诊断工具的用途,并讨论了回收率测定不确定性的来源。 [参考:8]

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