Article (Scientific journals)
Transfer of drug dissolution testing by statistical approaches: Case Study
AL-Kamarany, M. A.; EL Karbane, M.; Ridouan, K. et al.
2012In Saudi Pharmaceutical Journal, 20 (1), p. 93–101
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Keywords :
Accuracy profile; Dissolution test; Total error; Transfer; Statistics approach
Abstract :
[en] The analytical transfer is a complete process that consists in transferring an analytical procedure from a sending laboratory to a receiving laboratory. After having experimentally demonstrated that also masters the procedure in order to avoid problems in the future. Method of transfers is now commonplace during the life cycle of analytical method in the pharmaceutical industry. No official guideline exists for a transfer methodology in pharmaceutical analysis and the regulatory word of transfer is more ambiguous than for validation. Therefore, in this study, Gauge repeatability and reproducibility (R&R) studies associated with other multivariate statistics appropriates were successfully applied for the transfer of the dissolution test of diclofenac sodium as a case study from a sending laboratory A (accredited laboratory) to a receiving laboratory B. The HPLC method for the determination of the percent release of diclofenac sodium in solid pharmaceutical forms (one is the discovered product and another generic) was validated using accuracy profile (total error) in the sender laboratory A. The results showed that the receiver laboratory B masters the test dissolution process, using the sameHPLC analytical procedure developed in laboratory A. In conclusion, if the sender used the total error to validate its analytical method, dissolution test can be successfully transferred without mastering the analytical method validation by receiving laboratory B and the pharmaceutical analysis method state should be maintained to ensure the same reliable results in the receiving laboratory.
Research center :
CIRM - Centre Interdisciplinaire de Recherche sur le Médicament - ULiège
Disciplines :
Pharmacy, pharmacology & toxicology
Author, co-author :
AL-Kamarany, M. A.;  Mohammed V University, Soussi, > Faculty of Medicine and Pharmacy > Laboratory of Pharmacology and Toxicology
EL Karbane, M.;  Mohammed V University, Soussi, > Faculty of Medicine and Pharmacy > Laboratory of Pharmacology and Toxicology
Ridouan, K.;  Laboratory of Pharmacology and Toxicology > Faculty of Medecine and Pharmacy > Laboratory of Pharmacology and Toxicology
Alanazi, F. K.;  King Saud University > College of Pharmacy > Department of Pharmaceutics
Hubert, Philippe  ;  Université de Liège - ULiège > Département de pharmacie > Chimie analytique
Cherrah, Y.;  Mohammed V University, Soussi > Faculty of Medecine and Pharmay > Laboratory of Pharmacology and Toxicology
Bouklouze, A.;  Mohammed V University, Soussi, > Faculty od Medecine and Pharmacy > Laboratory of Pharmacology and Toxicology
Language :
English
Title :
Transfer of drug dissolution testing by statistical approaches: Case Study
Publication date :
January 2012
Journal title :
Saudi Pharmaceutical Journal
ISSN :
1319-0164
Publisher :
Elsevier
Volume :
20
Issue :
1
Pages :
93–101
Peer reviewed :
Peer Reviewed verified by ORBi
Available on ORBi :
since 08 January 2012

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