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Pharmaceutical analysis model robustness from Bagging-PLS and PLS using systematic tracking mapping

机译:Bagging-PLS和PLS使用系统跟踪映射的药物分析模型的鲁棒性

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Our work proved that processing trajectory could effectively obtain a more reliable and robust quantitative model compared with the step-by-step optimization method. The use of systematic tracking was investigated as a tool to optimize parameters in a quantitative model including spectral pretreatment, latent factors, variable selection and calibration method. The variable was selected by interval partial least-squares (iPLS), backward interval partial least-square (BiPLS) and synergy interval partial least-squares (SiPLS). The models were established by Partial least squares (PLS) and Bagging-PLS. The model performance was assessed by using the root mean square errors of validation (RMSEP) and the ratio of standard error of prediction to standard deviation (RPD). The proposed procedure was used to develop the models for near infrared (NIR) datasets of active pharmaceutical ingredients in tablets and chlorogenic acid of Lonicera japonica solution in ethanol precipitation process. The results demonstrated the feasibility and advantages of processing trajectory in the development and optimization of multivariate calibration models as well as the effectiveness of bagging model and variable selection to improve prediction accuracy and robustness.
机译:我们的工作证明,与逐步优化方法相比,加工轨迹可以有效地获得更可靠,更可靠的定量模型。研究了使用系统跟踪作为优化定量模型中参数的工具,包括光谱预处理,潜在因子,变量选择和校准方法。通过区间偏最小二乘(iPLS),向后区间偏最小二乘(BiPLS)和协同区间偏最小二乘(SiPLS)选择变量。通过偏最小二乘(PLS)和Bagging-PLS建立模型。通过使用验证的均方根误差(RMSEP)和预测标准误差与标准偏差(RPD)的比率来评估模型性能。拟议的程序用于建立片剂中活性成分的近红外(NIR)数据模型和乙醇沉淀过程中忍冬忍冬溶液的绿原酸数据模型。结果证明了加工轨迹在多元校准模型开发和优化中的可行性和优势,以及装袋模型和变量选择对​​提高预测准确性和鲁棒性的有效性。

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