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- Publications
- Influence
Biowaiver monographs for immediate release solid oral dosage forms: prednisone.
- M. Vogt, H. Derendorf, +6 authors D. Barends
- Medicine
- Journal of pharmaceutical sciences
- 1 June 2007
Literature data relevant to the decision to allow a waiver of in vivo bioequivalence (BE) testing for the approval of immediate release (IR) solid oral dosage forms containing prednisone are… Expand
Dissolution Testing as a Prognostic Tool for Oral Drug Absorption: Dissolution Behavior of Glibenclamide
- R. Löbenberg, J. Krämer, V. Shah, G. Amidon, J. Dressman
- Medicine
- Pharmaceutical Research
- 1 April 2000
Purpose. The dissolution behavior of two commercially availableglibenclamide formulations was tested in various media. The aim of thestudy was to investigate whether the use of biorelevant… Expand
Biowaiver Monographs for Immediate-Release Solid Oral Dosage Forms: Nifedipine.
- Jayachandar Gajendran, J. Krämer, +7 authors J. Dressman
- Chemistry, Medicine
- Journal of pharmaceutical sciences
- 1 October 2015
Literature data relevant to the biopharmaceutical properties of the active pharmaceutical ingredient (API) nifedipine are reviewed to evaluate whether a waiver of in vivo bioequivalence (BE) testing… Expand
In Vitro Performance Testing of Medicated Chewing Gums
- Lisa Zieschang, M. Klein, J. Krämer, M. Windbergs
- Chemistry
- 2018
The oromucosal route of therapeutic administration can be targeted by medicated chewing gums (MCGs) loaded with locally or systemically acting active pharmaceutical ingredients (API). Compared to… Expand
Biowaiver monographs for immediate release solid oral dosage forms: prednisolone.
- M. Vogt, H. Derendorf, +6 authors D. Barends
- Medicine, Chemistry
- Journal of pharmaceutical sciences
- 2007
Literature data relevant to the decision to allow a waiver of in vivo bioequivalence (BE) testing for the approval of immediate release (IR) solid oral dosage forms containing prednisolone are… Expand
Towards Standardized Dissolution Techniques for In Vitro Performance Testing of Dry Powder Inhalers
- A. Floroiu, M. Klein, J. Krämer, C. Lehr
- Chemistry
- 2018
The pulmonary route of administration is used for both locally and systemically acting drugs. However, knowledge gaps about the fate of aerosol particles after deposition in the lung provide room for… Expand
In Situ Drug Release Monitoring with a Fiber-Optic System: Overcoming Matrix Interferences Using Derivative Spectrophotometry
- A. Guillot, M. Limberger, J. Krämer, C. Lehr
- Chemistry
- 2013
The use of automation has increased in all the fields of the pharmaceutical industry, such as manufacturing and quality control. In the field of in vitro dissolution testing, the fiber-optic system… Expand
Dissolution Testing in Drug Product Development: Workshop Summary Report
- Andreas M Abend, David Curran, +17 authors Sandra Suarez-Sharp
- Computer Science, Medicine
- The AAPS Journal
- 28 January 2019
This publication summarizes the proceedings and key outcomes of the first day (“Day 1”) of the 3-day workshop on “Dissolution and Translational Modeling Strategies Enabling Patient-Centric Product… Expand
[Relative bioavailability of paracetamol in suppositories preparations in comparison to tablets].
- H. Blume, S. L. Ali, M. Elze, J. Krämer, G. Wendt, M. E. Scholz
- Chemistry, Medicine
- Arzneimittel-Forschung
- 1 December 1994
Relative Bioavailability of Paracetamol as Suppositories Compared to Tablets. The relative bioavailability of paracetamol (CAS 103-90-2) in ben-u-ron 500 mg and ben-u-ron 1000 mg suppositories (test… Expand
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