Vibrational spectroscopy; silicone-based drug reservoirs; Quality by Design; Process Analytical Technology; Chemometrics; Validation
Abstract :
[en] Using Near Infrared (NIR) and Raman spectroscopy as PAT tools, 3 critical quality attributes of a silicone-based drug reservoir were studied. First, the Active Pharmaceutical Ingredient (API) homogeneity in the reservoir was evaluated using Raman spectroscopy (mapping): the API distribution within the industrial drug reservoirs was found to be homogeneous while API aggregates were detected in laboratory scale samples manufactured with a non optimal mixing process. Second, the crosslinking process of the reservoirs was monitored at different temperatures with NIR spectroscopy. Conformity tests and Principal Component Analysis (PCA) were performed on the collected data to find out the relation between the temperature and the time necessary to reach the crosslinking endpoints. An agreement was found between the conformity test results and the PCA results. Compared to the conformity test method, PCA had the advantage to discriminate the heating effect from the crosslinking effect occurring together during the monitored process. Therefore the 2 approaches were found to be complementary. Third, based on the HPLC reference method, a NIR model able to quantify the API in the drug reservoir was developed and thoroughly validated. Partial Least Squares (PLS) regression on the calibration set was performed to build prediction models of which the ability to quantify accurately was tested with the external validation set. The 1.2 % RMSEP of the NIR model indicated the global accuracy of the model. The accuracy profile based on tolerance intervals was used to generate a complete validation report. The 95 % tolerance interval calculated on the validation results indicated that each future result will have a relative error below ±5 % with a probability of at least 95 %. In conclusion, 3 critical quality attributes of silicone-based drug reservoirs were quickly and efficiently evaluated by NIR and Raman spectroscopy.
Research Center/Unit :
C.I.R.M.
Disciplines :
Pharmacy, pharmacology & toxicology
Author, co-author :
Mantanus, Jérôme ; Université de Liège - ULiège > Département de pharmacie > Chimie analytique
Rozet, Eric ; Université de Liège - ULiège > Département de pharmacie > Chimie analytique
Van Butsele, K.; Odyssea pharma
De Bleye, Charlotte ; Université de Liège - ULiège > 2e an. master sc. pharm., fin. approf.
Ceccato, Attilio ; Université de Liège - ULiège > Département de pharmacie > Analyse des médicaments
Evrard, Brigitte ; Université de Liège - ULiège > Département de pharmacie > Pharmacie galénique
Hubert, Philippe ; Université de Liège - ULiège > Département de pharmacie > Chimie analytique
Ziemons, Eric ; Université de Liège - ULiège > Département de pharmacie > Département de pharmacie
Language :
English
Title :
Near infrared and Raman spectroscopy as Process Analytical Technology tools for the manufacturing of silicone-based drug reservoirs
Publication date :
2011
Journal title :
Analytica Chimica Acta
ISSN :
0003-2670
eISSN :
1873-4324
Publisher :
Elsevier, Amsterdam, Netherlands
Volume :
699
Pages :
96-106
Peer reviewed :
Peer Reviewed verified by ORBi
Funders :
DGTRE - Région wallonne. Direction générale des Technologies, de la Recherche et de l'Énergie F.R.S.-FNRS - Fonds de la Recherche Scientifique
International Conference on Harmonisation (ICH) of Technical Requirements for Registration of Pharmaceuticals for Human Use, Topic Q8(R2) 2009, Pharmaceutical Development, Geneva.
Tabasi S.H., Fahmy R., Bensley D., O'brien C., Hoag S.W. J. Pharm. Sci. 2008, 97:4040-4051.
International Conference on Harmonisation (ICH) of Technical Requirements for Registration of Pharmaceuticals for Human Use, Topic Q10 2008, Pharmaceutical Quality System, Geneva.
Kunzler J.F. Trends Polym. Sci. 1996, 4:52-59.
Chen Z., Ward R., Tian Y., Malizia F., Gracias D.H., Shen Y.R. J. Biomed. Mater. Res. 2002, 62:254-264.
United States Food and Drug Administration (FDA) Guidance for Industry PAT-A Framework for Innovative Pharmaceutical Manufacturing and Quality Assurance 2004, FDA.
Li X. Design of Controlled Release Drug Delivery Systems 2005, McGraw-Hill Professional, New York. first ed.
United States Food and Drug Administration (FDA) Pharmaceutical CGMPs for the 21st Century - A Risk-based Approach 2004, FDA.
Burns D.A., Ciurczak E.W. Handbook of Near-Infrared Analysis 2008, CRC Press, New York. third ed.
Luypaert J., Massart D.L., Vander Heyden Y. Talanta 2007, 72:865-883.
Sasic S. Pharmaceutical Applications of Raman Spectroscopy 2007, John Wiley & Sons, New Jersey.
International Conference on Harmonization (ICH) of Technical Requirements for Registration of Pharmaceuticals for Human Use, Topic Q2 (R1) 2005, Validation of Analytical Procedures: Text and Methodology, Geneva.
Hubert Ph., Nguyen-Huu J.J., Boulanger B., Chapuzet E., Chiap P., Cohen N., Compagnon P.A., Dewé W., Feinberg M., Lallier M., Laurentie M., Mercier N., Muzard G., Nivet C., Valat L. J. Pharm. Biomed. Anal. 2004, 36:579-586. http://hdl.handle.net/2268/6169.