Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Bernd Ulrich Riebesehl"'
Autor:
Bernard Van Eerdenbrugh, Bernd Ulrich Riebesehl, Arnaud Grandeury, Oksana Tsinman, Saijie Zhu, Konstantin Tsinman, Michael Juhnke, Ram Lingamaneni
Publikováno v:
Pharmaceutical Research. 35
The goal of the study was to evaluate a miniaturized dissolution-permeation apparatus (μFLUX™ apparatus) for its ability to benchmark several itraconazole (ITZ) formulations for which in vivo PK data was available in the literature. Untreated and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::04d70638e99bda9edf3325bb37b212d1
https://doi.org/10.1007/s11095-018-2440-3
https://doi.org/10.1007/s11095-018-2440-3
Autor:
Yi Zhang, Thomas Kissel, Bernd Ulrich Riebesehl, Moritz Beck-Broichsitter, Dafeng Chu, Catherine Curdy
Publikováno v:
European Journal of Pharmaceutics and Biopharmaceutics. 85:1232-1237
Cholesterol esterase (CE) induced surface erosion of poly(ethylene carbonate) (PEC) and drug release from PEC under mild physiological environment was investigated. The degradation process was monitored by changes of mass and molecular weight (MW) an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2279e7c85a3aad75c5b16c58f0db938a
https://doi.org/10.1016/j.ejpb.2013.04.011
https://doi.org/10.1016/j.ejpb.2013.04.011
Autor:
Bernd Ulrich Riebesehl
The choices for drug delivery options based on organic solvents and colloidal dispersed systems are discussed by route of administration. Key physicochemical properties and dosage forms of marketed oral and parenteral drugs are exemplified. For oral
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::21c4789307b9ed35e46187432a91e0fe
https://doi.org/10.1016/b978-0-12-417205-0.00029-8
https://doi.org/10.1016/b978-0-12-417205-0.00029-8
Publikováno v:
International journal of pharmaceutics. 465(1-2)
Macrophage induced surface degradation of poly(ethylene carbonate) (PEC) was investigated under in vitro conditions. Degradation of PEC with the MW of 41 kDa (PEC41) was slower than that of PEC with the MW of 200 kDa (PEC200). In terms of macrophage
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0760be1c576256f1910f884e4e07fe5
https://pubmed.ncbi.nlm.nih.gov/24530387
https://pubmed.ncbi.nlm.nih.gov/24530387
Autor:
Nathalie M. Pinkerton, Robert K. Prud'homme, Bernd Ulrich Riebesehl, Arnaud Grandeury, Jörg Brozio, Andreas Fisch
Publikováno v:
Molecular pharmaceutics. 10(1)
We present an in situ hydrophobic salt forming technique for the encapsulation of weakly hydrophobic, ionizable active pharmaceutical ingredients (API) into stable nanocarriers (NCs) formed via a rapid precipitation process. Traditionally, NC formati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b51342a18c554f458579319fc7faadfb
https://pubmed.ncbi.nlm.nih.gov/23259920
https://pubmed.ncbi.nlm.nih.gov/23259920