Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Xavier Lories"'
Autor:
Pierre-François Chavez, Fanny Stauffer, Frédéric Eeckman, Nils Bostijn, David Didion, Cédric Schaefer, Hong Yang, Yousef El Aalamat, Xavier Lories, Martin Warman, Benoit Mathieu, Jérôme Mantanus
Publikováno v:
International journal of pharmaceutics. 624
This paper describes the specific control strategy of the commercial manufacturing process of an immediate release tablet formulation based on continuous twin-screw wet granulation. This control strategy has been defined by a multidisciplinary team u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0cb3a4a06f96e2e2f4841c11442493ad
https://pubmed.ncbi.nlm.nih.gov/35781027
https://pubmed.ncbi.nlm.nih.gov/35781027
Autor:
Bruno Boulanger, Eric Rozet, Perceval Sondag, Jean-François Michiels, Pierre Lebrun, Xavier Lories
Publikováno v:
Statistics for Biotechnology Process Development ISBN: 9781315120034
Optimizing a formulation buffer for biological products such as vaccines or monoclonal antibodies is a complex task. One of the reasons for this is that the number of formulation ingredients make it difficult to cost efficiently design experiments. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::faf84e81c2ed71d91800f44a49040a63
https://doi.org/10.1201/9781315120034-3
https://doi.org/10.1201/9781315120034-3
Publikováno v:
Computational and Theoretical Chemistry. 966:244-249
Strain has been defined as a source of errors in the determination of heats of formations using bond separation reactions. In this work, we define Ring Conserving Isodesmic Reactions to conserve the strain. First a set of reference systems is defined
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::51f0f0e4bc17157303c684c4fb9300e7
https://doi.org/10.1016/j.comptc.2011.03.007
https://doi.org/10.1016/j.comptc.2011.03.007
Publikováno v:
International Journal of Quantum Chemistry. 112:1959-1967
In this work, the isomerization mechanisms of dehydrofulvene radicals to the phenyl radical are described. This study shows, for 6-dehydrofulvene, a low-energy isomerization path going through a resonantly stabilized bicyclic system. In a second part
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6649b1700298021f238682f44b1b53fe
https://doi.org/10.1002/qua.23142
https://doi.org/10.1002/qua.23142
Publikováno v:
International Journal of Quantum Chemistry. 112:540-550
In this work, we define an isodesmicity index, which allows the evaluation of the conservation of the error within a given bond conserving reaction. This index is reaction-specific and, therefore, does not rely on the nature of the reference systems.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::57c4870b94a5abd6785b9084952fd62e
https://doi.org/10.1002/qua.23035
https://doi.org/10.1002/qua.23035
Publikováno v:
Combustion Science and Technology. 182:350-364
Experimental structures of two dimethoxymethane/oxygen/argon flames at equivalence ratios of phi = 0.24 and 1.72 have been studied by mass spectrometry. The detected species throughout the flame thickness were H-2, CH3, CH4, H2O, C2H2, CO, CH2O, CH3O
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::710563fae9eb33748923ddb49670a5c1
https://doi.org/10.1080/00102200903462458
https://doi.org/10.1080/00102200903462458
Publikováno v:
Chemical Physics Letters. 452:29-32
The experimental value for the heat of formation of fulvene is 53.6 or 53.5 kcal mol(-1) depending on the source. However, no theoretical calculation seems to reproduce that value. In this work, we deduce the heat of formation of fulvene from high-le
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::82b33878db9c10178f44e73c1b348b01
https://doi.org/10.1016/j.cplett.2007.12.033
https://doi.org/10.1016/j.cplett.2007.12.033
Publikováno v:
Physical chemistry chemical physics : PCCP. 12(15)
Various reactions following acetylene addition on i- and n-C(4)H(3) radicals are studied using a modified G3B3 method. For the addition of C(2)H(2) on n-C(4)H(3), the commonly admitted phenyl radical decomposition path of Madden and coworkers has bee
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::acbce1de2b92d7562f7902ec346b8fce
https://pubmed.ncbi.nlm.nih.gov/20358071
https://pubmed.ncbi.nlm.nih.gov/20358071