Moisture content determination in an antibody-drug conjugate freeze-dried medicine by near-infrared spectroscopy: A case study for release testing

被引:16
作者
Clavaud, Matthieu [1 ,2 ]
Roggo, Yves [1 ]
Degardin, Klara [1 ]
Sacre, Pierre-Yves [2 ]
Hubert, Philippe [2 ]
Ziemons, Eric [2 ]
机构
[1] F Hoffmann La Roche Ltd, Bldg 250 Room 3-504-01, CH-4303 Kaiseraugst, Switzerland
[2] Univ Liege ULg, Quartier Hop, Dept Pharm, Analyt Chem Lab, Ave Hippocrate 15,B36, B-4000 Liege, Belgium
关键词
Antibody-drug conjugate; Freeze-dried medicine; Moisture content; Near-infrared spectroscopy; Partial least squares regression; Validation; FORMULATIONS; VALIDATION; STABILITY; WATER; CHEMOMETRICS;
D O I
10.1016/j.jpba.2016.09.014
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The use of Near-infrared spectroscopy (NIRS) as a fast and non-destructive technique was employed for moisture content (MC) determination in Antibody-drug conjugates (ADCs) in replacement to Karl Fischer (KF) method. The lab analysis of ADCs, high potent medicines, should be performed in conditions ensuring the operator's safety and using secured analytical tools like NIRS. A NIRS method was first developed and validated in compliance with current guidelines. The novelty of this work first lies in the large number of samples prepared for a wide moisture calibration range of 0.51%-4.01%. Then, the classical Partial Least Square (PLS) regression was used as chemometric tool for the computation of the model. Excellent predictive calibration results were shown. A coefficient of correlation (r) value of 0.99 was obtained. An intercept value of 0.02 and a slope of 0.99 were observed, while the root mean square error of calibration (RMSEC) and the root mean square error of prediction (RMSEP) were respectively 0.10% and 0.12%. In addition, instrumentation, model performances and robustness of the method were evaluated, demonstrating the validation results. Calibration transfer issue and impact of the number of samples were also evaluated. Consequently, a validation strategy was introduced as a basis for submission to the health authorities' for release and stability activities in a cGMP environment in replacement of the KF method. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:380 / 390
页数:11
相关论文
共 42 条
[1]   Role of water in the physical stability of solid dosage formulations [J].
Airaksinen, S ;
Karjalainen, M ;
Shevchenko, A ;
Westermarck, S ;
Leppänen, E ;
Rantanen, J ;
Yliruusi, J .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2005, 94 (10) :2147-2165
[2]  
[Anonymous], 2012, E165505 ASTM
[3]  
[Anonymous], 2010, 120992010E ISO
[4]  
[Anonymous], 2004, Food and Drug Administration Guidance for industry PATa framework for innovative pharmaceutical development, manufacturing and quality Assurance
[5]  
[Anonymous], 2016, CHEM METH APPL AN DA
[6]  
[Anonymous], 2016, NEAR INFRARED SPECTR
[7]   Plant analysis using near infrared reflectance spectroscopy: the potential and the limitations [J].
Batten, GD .
AUSTRALIAN JOURNAL OF EXPERIMENTAL AGRICULTURE, 1998, 38 (07) :697-706
[8]   Critical review of chemometric indicators commonly used for assessing the quality of the prediction of soil attributes by NIR spectroscopy [J].
Bellon-Maurel, Veronique ;
Fernandez-Ahumada, Elvira ;
Palagos, Bernard ;
Roger, Jean-Michel ;
McBratney, Alex .
TRAC-TRENDS IN ANALYTICAL CHEMISTRY, 2010, 29 (09) :1073-1081
[9]  
Cogdill RP., 2006, Spectroscopy of Pharmaceutical Solids, V1, P313
[10]   Formulation and delivery issues for monoclonal antibody therapeutics [J].
Daugherty, Ann L. ;
Mrsny, Randall J. .
ADVANCED DRUG DELIVERY REVIEWS, 2006, 58 (5-6) :686-706