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Gert Fricker

Showing results (131-140 of 193) with videos related to

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Journal of Medicinal Chemistry|January 28, 2009
Potent and selective inhibitors of breast cancer resistance protein (ABCG2) derived from the p-glycoprotein (ABCB1) modulator tariquidarMatthias Kühnle, Michael Egger, Christine Müller, et al.
Neurobiology of Disease|April 26, 2022
Altered protein expression of membrane transporters in isolated cerebral microvessels and brain cortex of a rat Alzheimer's disease modelElena Puris, Seppo Auriola, Sabrina Petralla, et al.
Journal of Pharmaceutical Sciences|October 22, 2014
Improved oral bioavailability of human growth hormone by a combination of liposomes containing bio-enhancers and tetraether lipids and omeprazoleJohannes Parmentier, Götz Hofhaus, Silke Thomas, et al.
Drug Design, Development and Therapy|July 2, 2020
Sugar Codes Conjugated Alginate: An Innovative Platform to Make a Strategic Breakthrough in Simultaneous Prophylaxis of GERD and <i>Helicobacter pylori</i> InfectionSaeed Moayedi, Abbas Yadegar, Saeed Balalaie, et al.
Journal of Pharmaceutical Sciences|April 26, 2014
What is the mechanism behind increased permeation rate of a poorly soluble drug from aqueous dispersions of an amorphous solid dispersion?Kerstin J Frank, Ulrich Westedt, Karin M Rosenblatt, et al.
European Journal of Pharmaceutics and Biopharmaceutics : Official Journal of Arbeitsgemeinschaft Fur Pharmazeutische Verfahrenstechnik E.V|June 12, 2020
Physicochemical and biopharmaceutical characterization of novel Matrix-LiposomesMichael Binnefeld, Sandra Fritz, Viktor Balzer, et al.
International Journal of Nanomedicine|November 21, 2012
The amorphous solid dispersion of the poorly soluble ABT-102 forms nano/microparticulate structures in aqueous medium: impact on solubilityKerstin J Frank, Ulrich Westedt, Karin M Rosenblatt, et al.
European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences|May 15, 2012
Impact of FaSSIF on the solubility and dissolution-/permeation rate of a poorly water-soluble compoundKerstin J Frank, Ulrich Westedt, Karin M Rosenblatt, et al.
European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences|July 19, 2017
Oral delivery of vancomycin by tetraether lipid liposomesPhilipp Uhl, Silvia Pantze, Philip Storck, et al.
International Journal of Pharmaceutics|August 25, 2016
Delivery of Copper-chelating Trientine (TETA) to the central nervous system by surface modified liposomesRobin Tremmel, Philipp Uhl, Frieder Helm, et al.
Pageof 20

Showing results (131-140 of 193) with videos related to

Sort By:
Pageof 20
Journal of Medicinal Chemistry|January 28, 2009
Potent and selective inhibitors of breast cancer resistance protein (ABCG2) derived from the p-glycoprotein (ABCB1) modulator tariquidarMatthias Kühnle, Michael Egger, Christine Müller, et al.
Neurobiology of Disease|April 26, 2022
Altered protein expression of membrane transporters in isolated cerebral microvessels and brain cortex of a rat Alzheimer's disease modelElena Puris, Seppo Auriola, Sabrina Petralla, et al.
Journal of Pharmaceutical Sciences|October 22, 2014
Improved oral bioavailability of human growth hormone by a combination of liposomes containing bio-enhancers and tetraether lipids and omeprazoleJohannes Parmentier, Götz Hofhaus, Silke Thomas, et al.
Drug Design, Development and Therapy|July 2, 2020
Sugar Codes Conjugated Alginate: An Innovative Platform to Make a Strategic Breakthrough in Simultaneous Prophylaxis of GERD and <i>Helicobacter pylori</i> InfectionSaeed Moayedi, Abbas Yadegar, Saeed Balalaie, et al.
Journal of Pharmaceutical Sciences|April 26, 2014
What is the mechanism behind increased permeation rate of a poorly soluble drug from aqueous dispersions of an amorphous solid dispersion?Kerstin J Frank, Ulrich Westedt, Karin M Rosenblatt, et al.
European Journal of Pharmaceutics and Biopharmaceutics : Official Journal of Arbeitsgemeinschaft Fur Pharmazeutische Verfahrenstechnik E.V|June 12, 2020
Physicochemical and biopharmaceutical characterization of novel Matrix-LiposomesMichael Binnefeld, Sandra Fritz, Viktor Balzer, et al.
International Journal of Nanomedicine|November 21, 2012
The amorphous solid dispersion of the poorly soluble ABT-102 forms nano/microparticulate structures in aqueous medium: impact on solubilityKerstin J Frank, Ulrich Westedt, Karin M Rosenblatt, et al.
European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences|May 15, 2012
Impact of FaSSIF on the solubility and dissolution-/permeation rate of a poorly water-soluble compoundKerstin J Frank, Ulrich Westedt, Karin M Rosenblatt, et al.
European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences|July 19, 2017
Oral delivery of vancomycin by tetraether lipid liposomesPhilipp Uhl, Silvia Pantze, Philip Storck, et al.
International Journal of Pharmaceutics|August 25, 2016
Delivery of Copper-chelating Trientine (TETA) to the central nervous system by surface modified liposomesRobin Tremmel, Philipp Uhl, Frieder Helm, et al.
Pageof 20