首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Application of quality by design concept to develop a dual gradient elution stability-indicating method for cloxacillin forced degradation studies using combined mixture-process variable models
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Application of quality by design concept to develop a dual gradient elution stability-indicating method for cloxacillin forced degradation studies using combined mixture-process variable models

机译:设计概念的应用在利用组合混合物 - 过程变量模型开发了一种开发了一种双梯度洗脱稳定性指示方法

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Penicillins are typical of complex ionic samples which likely contain large number of degradation-related impurities (DRIs) with different polarities and charge properties. It is often a challenge to develop selective and robust high performance liquid chromatography (HPLC) methods for the efficient separation of all DRIs. In this study, an analytical quality by design (AQbD) approach was proposed for stability indicating method development of cloxacillin. The structures, retention and UV characteristics rules of penicillins and their impurities were summarized and served as useful prior knowledge. Through quality risk assessment and screen design, 3 critical process parameters (CPPs) were defined, including 2 mixture variables (MVs) and 1 process variable (PV). A combined mixture-process variable (MPV) design was conducted to evaluate the 3 CPPs simultaneously and a response surface methodology (RSM) was used to achieve the optimal experiment parameters. A dual gradient elution was performed to change buffer pH, mobile-phase type and strength simultaneously. The design spaces (DSs) was evaluated using Monte Carlo simulation to give their possibility of meeting the specifications of CQAs. A Plackett-Burman design was performed to test the robustness around the working points and to decide the normal operating ranges (NORs). Finally, validation was performed following International Conference on Harmonisation (ICH) guidelines. To our knowledge, this is the first study of using MPV design and dual gradient elution to develop HPLC methods and improve separations for complex ionic samples. (C) 2017 Elsevier B.V. All rights reserved.
机译:青霉素是典型的复杂离子样本,其可能含有大量的有关相关的杂质(DRIS),具有不同的极性和电荷性能。开发选择性和稳健的高效液相色谱(HPLC)方法往往是一个挑战,以便有效地分离所有DRIS。在这项研究中,提出了通过设计(AQBD)方法的分析质量,用于克罗克里林的稳定性指示方法开发。总结了青霉素的结构,保留和UV特征规则及其杂质,并作为有用的先验知识。通过质量风险评估和屏幕设计,定义了3个关键过程参数(CPP),包括2个混合物变量(MV)和1个过程变量(PV)。进行组合的混合物 - 过程变量(MPV)设计以同时评估3个CPP,并使用响应表面方法(RSM)来实现最佳实验参数。进行双重梯度洗脱以同时进行缓冲液pH,移动相类型和强度。使用Monte Carlo仿真评估设计空间(DSS),以满足CQAS规格的可能性。进行Plackett-Burman设计以测试工作点周围的稳健性,并决定正常操作范围(nors)。最后,在协调会议上进行验证(ICH)指导方针进行。据我们所知,这是第一次使用MPV设计和双重梯度洗脱来开发HPLC方法的研究,并改善复杂离子样品的分离。 (c)2017年Elsevier B.V.保留所有权利。

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