Zobrazeno 1 - 10
of 261
pro vyhledávání: '"E, Rozet"'
Autor:
RD Marini, Nathalie Dubois, MP Ndelo, E Rozet, JP Ndelo, P Le Brun, MM Lusakibanza, Mlc Mputu, KR Cimanga, Corinne Charlier
Publikováno v:
Journal of Toxicology and Risk Assessment. 5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::88b3f090fe390e4063579cf0600a061b
https://doi.org/10.23937/2572-4061.1510030
https://doi.org/10.23937/2572-4061.1510030
Autor:
F, Lecomte, J, Aerts, A, Plenevaux, C, Defraiteur, F, Chapuis-Hugon, E, Rozet, P, Chiap, A, Luxen, V, Pichon, Ph, Hubert, C, Hubert
Publikováno v:
Journal of pharmaceutical and biomedical analysis. 180
Within the family of serotonin (5-HT) receptors, the 5-HT
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c32dda627c87082231ac66ecdddbb33e
https://pubmed.ncbi.nlm.nih.gov/31865206
https://pubmed.ncbi.nlm.nih.gov/31865206
Autor:
André Luxen, Frédéric Lecomte, Alain Plenevaux, C. Defraiteur, Ph. Hubert, Valérie Pichon, F. Chapuis-Hugon, J. Aerts, Patrice Chiap, E. Rozet, Cédric Hubert
Publikováno v:
Journal of Pharmaceutical and Biomedical Analysis. 180:113015
Within the family of serotonin (5-HT) receptors, the 5-HT1A subtype is particularly interesting as it may be involved in various physiological processes or psychological disorders. The p-[18F]MPPF, a highly selective 5-HT1A antagonist, is used for in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d204b40a24aae69cf300317f0af7f42d
https://doi.org/10.1016/j.jpba.2019.113015
https://doi.org/10.1016/j.jpba.2019.113015
Autor:
Amandine Dispas, Védaste Habyalimana, N. Kalenda, E. Rozet, Pierre Lebrun, J. Mavar Tayey Mbay, Jérémie Kindenge Mbinze, Roland Djang’eing’a Marini, Ph. Hubert
Publikováno v:
Journal of Pharmaceutical and Biomedical Analysis. 85:83-92
The poor quality of medicines is a crucial problem of public health. Therefore, it is important to have analytical tools to attend decisions of the legal authorities while combating this offense. In this context, the main objective of this study was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7dfacd673c56e73f4a03e884da8794b0
https://doi.org/10.1016/j.jpba.2013.06.036
https://doi.org/10.1016/j.jpba.2013.06.036
Publikováno v:
Analytica Chimica Acta. 760:46-52
Validation of analytical methods is required prior to their routine use. In addition, the current implementation of the Quality by Design (QbD) framework in the pharmaceutical industries aims at improving the quality of the end products starting from
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a4f22d8c6a01be882c27166121f405b
https://doi.org/10.1016/j.aca.2012.11.013
https://doi.org/10.1016/j.aca.2012.11.013
Autor:
Jérémie Kindenge Mbinze, Benjamin Debrus, J. Mavar Tayey Mbay, Amandine Dispas, Pierre Lebrun, Roland Djang’eing’a Marini, B. Boulanger, T. Schofield, Ph. Hubert, E. Rozet, N. Kalenda
Publikováno v:
Journal of Chromatography A. 1263:113-124
In the context of the battle against counterfeit medicines, an innovative methodology has been used to develop rapid and specific high performance liquid chromatographic methods to detect and determine 18 non-steroidal anti-inflammatory drugs, 5 phar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb90a3710652d3028181e2eb54afd7a1
https://doi.org/10.1016/j.chroma.2012.09.038
https://doi.org/10.1016/j.chroma.2012.09.038
Autor:
Ph. Hubert, M. El Karbane, A. Bouabidi, Mohammed Talbi, Y. Brik, H. Bourichi, B. Boulanger, E. Rozet, Abdelaziz Bouklouze
Publikováno v:
Drug Testing and Analysis. 4:1014-1027
An innovative versatile strategy using Total Error has been proposed to decide about the method's validity that controls the risk of accepting an unsuitable assay together with the ability to predict the reliability of future results. This strategy i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ab87c3ce447c75291b112b73ee775e1a
https://doi.org/10.1002/dta.1345
https://doi.org/10.1002/dta.1345
Autor:
Ph. Hubert, M. El Karbane, B. Boulanger, A. Bouabidi, Mohammed Talbi, E. Rozet, Abdelaziz Bouklouze, Cédric Hubert, H. Bourichi, Eric Ziemons, Roland Djang’eing’a Marini
Publikováno v:
Analytica Chimica Acta. 714:47-56
Analytical methods capability evaluation can be a useful methodology to assess the fitness of purpose of these methods for their future routine application. However, care on how to compute the capability indices have to be made. Indeed, the commonly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c79dcd520acd8e25745a60dfa791994
https://doi.org/10.1016/j.aca.2011.11.019
https://doi.org/10.1016/j.aca.2011.11.019
Publikováno v:
Journal of Pharmaceutical and Biomedical Analysis. 55:848-858
Bioanalytical method validation is a mandatory step to evaluate the ability of developed methods to provide accurate results for their routine application in order to trust the critical decisions that will be made with them. Even if several guideline
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b83089e9205de11e3ea28c0be00d6d62
https://doi.org/10.1016/j.jpba.2010.12.018
https://doi.org/10.1016/j.jpba.2010.12.018
Autor:
Eric Ziemons, E. Rozet, Roland Djang’eing’a Marini, Walthère Dewé, Philippe Hubert, B. Boulanger, Serge Rudaz
Publikováno v:
TrAC Trends in Analytical Chemistry. 30:797-806
Guidelines ISO 17025 and ISO 15189 aim to improve the quality-assurance scheme of laboratories. Reliable analytical results are of central importance due to the critical decisions that are taken with them. ISO 17025 and ISO 15189 therefore require th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a92de4d3fe180c1a8cad8adb756d98df
https://doi.org/10.1016/j.trac.2010.12.009
https://doi.org/10.1016/j.trac.2010.12.009