Comparison of impurity profiles of lipiblock® vs. orlistat using HPLC and LC-MS/MS


Autoria(s): Schneider, Alex; Wessjohann, Ludger A.; Severi, Juliana A.; Wagner, Vilegas
Contribuinte(s)

Universidade Estadual Paulista (UNESP)

Data(s)

27/05/2014

27/05/2014

30/04/2012

Resumo

Comparative HPLC-UV and LC-MS/MS studies of impurity profiles of a reference sample (Xenical®, F. Hoffmann-La Roche Ltd., Switzerland) vs. generic (Lipiblock®, EMS-Sigma Pharma, a generic drug) were carried out with ethanol extracts of commercial samples. The generic formulation contained higher levels of common impurities as well as a considerable number of impurities not found in the reference product. The detected impurity profile of Lipiblock® revealed that it most likely is based on fermentation. Since the effect of the impurities is unknown, at this point fully synthetic Xenical® appears to offer a better safety margin than Lipiblock® which, however, compares quite well to other generic formulations.

Formato

91-96

Identificador

http://www.latamjpharm.org/resumenes/31/1/LAJOP_31_1_1_14.pdf

Latin American Journal of Pharmacy, v. 31, n. 1, p. 91-96, 2012.

0326-2383

http://hdl.handle.net/11449/73298

2-s2.0-84860125323

Idioma(s)

eng

Relação

Latin American Journal of Pharmacy

Direitos

closedAccess

Palavras-Chave #Generics #HPLC-MS/MS #HPLC-UV #Orlistat #cobese #generic drug #lipiblock #orsoten #rotipuran #suprapur #tetrahydrolipstatin #unclassified drug #controlled study #drug formulation #drug impurity #drug safety #drug structure #fermentation #high performance liquid chromatography #intermethod comparison #liquid chromatography #mass spectrometry
Tipo

info:eu-repo/semantics/article