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W Peter Wuelfing

Showing results (1-10 of 29) with videos related to

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Molecular Pharmaceutics|March 8, 2012
Identification of suitable formulations for high dose oral studies in rats using in vitro solubility measurements, the maximum absorbable dose model, and historical data setsW Peter Wuelfing, Elizabeth Kwong, John Higgins
Journal of Pharmaceutical Sciences|August 8, 2020
Base-Mediated Oxidative Degradation of Secondary Amides Derived from p-Amino Phenol to Primary Amides in Drug MoleculesKausik K Nanda, Anthony Ginnetti, W Peter Wuelfing
Journal of Chromatography. A|March 4, 2019
Mechanistic understanding of abnormal reverse phase chromatographic behavior of basic analytes in the presence of sodium dodecyl sulfateAdam Socia, Yong Liu, Andreas Abend, et al.
Journal of Pharmaceutical and Biomedical Analysis|November 1, 2005
Profiling of medium chain glycerides used in pharmaceutical formulation development by reversed-phase HPLCKyle A Fliszar, W Peter Wuelfing, Zhong Li, et al.
Journal of Pharmaceutical and Biomedical Analysis|April 2, 2003
Development and validation of an automated extraction method (accelerated solvent extraction) and a reverse-phase HPLC analysis method for assay of ivermectin in a meat-based chewable formulationAndreas M Abend, Le Chung, David G McCollum, et al.
Molecular Pharmaceutics|March 29, 2016
Mechanism of Dissolution-Induced Nanoparticle Formation from a Copovidone-Based Amorphous Solid DispersionPaul Harmon, Kendra Galipeau, Wei Xu, et al.
Journal of Separation Science|August 14, 2020
Development of an ultra-high-performance liquid chromatography-charged aerosol detection/UV method for the quantitation of linear polyethylenimines in oligonucleotide polyplexesAdam Socia, Yong Liu, Yuejie Zhao, et al.
Molecular Pharmaceutics|February 12, 2015
Preclinical dose number and its application in understanding drug absorption risk and formulation design for preclinical speciesW Peter Wuelfing, Pierre Daublain, Filippos Kesisoglou, et al.
Molecular Pharmaceutics|September 10, 2020
Probing Protein Conformation Destabilization in Sterile Liquid Formulations through the Formation of 3,4-DihydroxyphenylalanineOlivier Mozziconacci, Natalia Subelzu, Christian Schöneich, et al.
Journal of Pharmaceutical Sciences|October 14, 2018
In-Use Photostability Practice and Regulatory Evaluation for Pharmaceutical Products in an Age of Light-Emitting Diode Light SourcesLeonardo R Allain, Brittany C Pierce, W Peter Wuelfing, et al.
Pageof 3

Showing results (1-10 of 29) with videos related to

Sort By:
Pageof 3
Molecular Pharmaceutics|March 8, 2012
Identification of suitable formulations for high dose oral studies in rats using in vitro solubility measurements, the maximum absorbable dose model, and historical data setsW Peter Wuelfing, Elizabeth Kwong, John Higgins
Journal of Pharmaceutical Sciences|August 8, 2020
Base-Mediated Oxidative Degradation of Secondary Amides Derived from p-Amino Phenol to Primary Amides in Drug MoleculesKausik K Nanda, Anthony Ginnetti, W Peter Wuelfing
Journal of Chromatography. A|March 4, 2019
Mechanistic understanding of abnormal reverse phase chromatographic behavior of basic analytes in the presence of sodium dodecyl sulfateAdam Socia, Yong Liu, Andreas Abend, et al.
Journal of Pharmaceutical and Biomedical Analysis|November 1, 2005
Profiling of medium chain glycerides used in pharmaceutical formulation development by reversed-phase HPLCKyle A Fliszar, W Peter Wuelfing, Zhong Li, et al.
Journal of Pharmaceutical and Biomedical Analysis|April 2, 2003
Development and validation of an automated extraction method (accelerated solvent extraction) and a reverse-phase HPLC analysis method for assay of ivermectin in a meat-based chewable formulationAndreas M Abend, Le Chung, David G McCollum, et al.
Molecular Pharmaceutics|March 29, 2016
Mechanism of Dissolution-Induced Nanoparticle Formation from a Copovidone-Based Amorphous Solid DispersionPaul Harmon, Kendra Galipeau, Wei Xu, et al.
Journal of Separation Science|August 14, 2020
Development of an ultra-high-performance liquid chromatography-charged aerosol detection/UV method for the quantitation of linear polyethylenimines in oligonucleotide polyplexesAdam Socia, Yong Liu, Yuejie Zhao, et al.
Molecular Pharmaceutics|February 12, 2015
Preclinical dose number and its application in understanding drug absorption risk and formulation design for preclinical speciesW Peter Wuelfing, Pierre Daublain, Filippos Kesisoglou, et al.
Molecular Pharmaceutics|September 10, 2020
Probing Protein Conformation Destabilization in Sterile Liquid Formulations through the Formation of 3,4-DihydroxyphenylalanineOlivier Mozziconacci, Natalia Subelzu, Christian Schöneich, et al.
Journal of Pharmaceutical Sciences|October 14, 2018
In-Use Photostability Practice and Regulatory Evaluation for Pharmaceutical Products in an Age of Light-Emitting Diode Light SourcesLeonardo R Allain, Brittany C Pierce, W Peter Wuelfing, et al.
Pageof 3