Process Analytical Technology (PAT);
Near infrared spectroscopy;
On-line measurement;
Active pharmaceutical ingredient (API) crystallization;
BATCH COOLING CRYSTALLIZATION;
NIR SPECTROSCOPY;
AT-LINE;
CALIBRATION;
MODELS;
CHEMOMETRICS;
SCUTELLAREIN;
REGRESSION;
PLS;
D O I:
10.1016/j.jpba.2013.05.015
中图分类号:
O65 [分析化学];
学科分类号:
070302 ;
081704 ;
摘要:
The final step of an active pharmaceutical ingredient (API) manufacturing synthesis process consists of a crystallization during which the API and residual solvent contents have to be quantified precisely in order to reach a predefined seeding point. A feasibility study was conducted to demonstrate the suitability of on-line NIR spectroscopy to control this step in line with new version of the European Medicines Agency (EMA) guideline [1]. A quantitative method was developed at laboratory scale using statistical design of experiments (DOE) and multivariate data analysis such as principal component analysis (PCA) and partial least squares (PLS) regression. NIR models were built to quantify the API in the range of 9-12% (w/w) and to quantify the residual methanol in the range of 0-3% (w/w). To improve the predictive ability of the models, the development procedure encompassed: outliers elimination, optimum model rank definition, spectral range and spectral pre-treatment selection. Conventional criteria such as, number of PLS factors, R-2, root mean square errors of calibration, cross-validation and prediction (RMSEC, RMSECV, RMSEP) enabled the selection of three model candidates. These models were tested in the industrial pilot plant during three technical campaigns. Results of the most suitable models were evaluated against to the chromatographic reference methods. Maximum relative bias of 2.88% was obtained about API target content. Absolute bias of 0.01 and 0.02% (w/w) respectively were achieved at methanol content levels of 0.10 and 0.13% (w/w). The repeatability was assessed as sufficient for the on-line monitoring of the 2 analytes. The present feasibility study confirmed the possibility to use on-line NIR spectroscopy as a PAT tool to monitor in real-time both the API and the residual methanol contents, in order to control the seeding of an API crystallization at industrial scale. Furthermore, the successful scale-up of the method proved its capability to be implemented in the manufacturing plant with the launch of the new API process. (c) 2013 Elsevier B.V. All rights reserved.
机构:
Nankai Univ, Coll Pharm, State Key Lab Med Chem Biol, Tianjin Key Lab Mol Drug Res, Tianjin 300071, Peoples R ChinaNankai Univ, Coll Pharm, State Key Lab Med Chem Biol, Tianjin Key Lab Mol Drug Res, Tianjin 300071, Peoples R China
Ding, Guoyu
Hou, Yuanyuan
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Nankai Univ, Coll Pharm, State Key Lab Med Chem Biol, Tianjin Key Lab Mol Drug Res, Tianjin 300071, Peoples R ChinaNankai Univ, Coll Pharm, State Key Lab Med Chem Biol, Tianjin Key Lab Mol Drug Res, Tianjin 300071, Peoples R China
Hou, Yuanyuan
Peng, Jiamin
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Nankai Univ, Coll Pharm, State Key Lab Med Chem Biol, Tianjin Key Lab Mol Drug Res, Tianjin 300071, Peoples R ChinaNankai Univ, Coll Pharm, State Key Lab Med Chem Biol, Tianjin Key Lab Mol Drug Res, Tianjin 300071, Peoples R China
Peng, Jiamin
Shen, Yunbing
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Nankai Univ, Coll Pharm, State Key Lab Med Chem Biol, Tianjin Key Lab Mol Drug Res, Tianjin 300071, Peoples R ChinaNankai Univ, Coll Pharm, State Key Lab Med Chem Biol, Tianjin Key Lab Mol Drug Res, Tianjin 300071, Peoples R China
Shen, Yunbing
Jiang, Min
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Nankai Univ, Coll Pharm, State Key Lab Med Chem Biol, Tianjin Key Lab Mol Drug Res, Tianjin 300071, Peoples R ChinaNankai Univ, Coll Pharm, State Key Lab Med Chem Biol, Tianjin Key Lab Mol Drug Res, Tianjin 300071, Peoples R China
Jiang, Min
Bai, Gang
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Nankai Univ, Coll Pharm, State Key Lab Med Chem Biol, Tianjin Key Lab Mol Drug Res, Tianjin 300071, Peoples R ChinaNankai Univ, Coll Pharm, State Key Lab Med Chem Biol, Tianjin Key Lab Mol Drug Res, Tianjin 300071, Peoples R China
机构:
State Key Laboratory of Medicinal Chemical Biology, College of Pharmacy, Nankai UniversityState Key Laboratory of Medicinal Chemical Biology, College of Pharmacy, Nankai University
Guoyu Ding
Yuanyuan Hou
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State Key Laboratory of Medicinal Chemical Biology, College of Pharmacy, Nankai UniversityState Key Laboratory of Medicinal Chemical Biology, College of Pharmacy, Nankai University
Yuanyuan Hou
Jiamin Peng
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State Key Laboratory of Medicinal Chemical Biology, College of Pharmacy, Nankai UniversityState Key Laboratory of Medicinal Chemical Biology, College of Pharmacy, Nankai University
Jiamin Peng
Yunbing Shen
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机构:
State Key Laboratory of Medicinal Chemical Biology, College of Pharmacy, Nankai UniversityState Key Laboratory of Medicinal Chemical Biology, College of Pharmacy, Nankai University
Yunbing Shen
Min Jiang
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机构:
State Key Laboratory of Medicinal Chemical Biology, College of Pharmacy, Nankai UniversityState Key Laboratory of Medicinal Chemical Biology, College of Pharmacy, Nankai University
Min Jiang
Gang Bai
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机构:
State Key Laboratory of Medicinal Chemical Biology, College of Pharmacy, Nankai UniversityState Key Laboratory of Medicinal Chemical Biology, College of Pharmacy, Nankai University