Hochschulschrift
In vivo-relevant mini-scale biphasic dissolution model for the development of solid oral dosage forms
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Dimensions
-
21 cm
- Extent
-
176, XX Seiten
- Language
-
Englisch
- Notes
-
Illustrationen
Rheinische Friedfrich-Wilhelms-Universität zu Bonn, Dissertation, 2019
- Table of contents
- Rights
-
Bei diesem Objekt liegt nur das Inhaltsverzeichnis digital vor. Der Zugriff darauf ist unbeschränkt möglich.
- Last update
-
11.06.2025, 2:14 PM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Object type
- Hochschulschrift
Associated
Time of origin
- 2019
Other Objects (12)
Combined assessment of dissolution and epithelial permeability of solid oral dosage forms
Phospholipids as functional excipients in solid oral dosage forms
“Solidified liquid lipids” for oral solid dosage forms : characterisation and processing
Biopredictive disintegration and dissolution of solid oral dosage forms : biorelevant in vitro tests for enteric-coated dosage forms and development of fast dissolving pH-responsive polymers
Evaluation of multiple factors influencing the ability to swallow solid oral dosage forms
Liposomes as a solid dosage form and for the oral delivery of vancomycin
Biorelevant dissolution test methods for modified release dosage forms
Development of discriminative and predictive dissolution tests for immediate release oral dosage forms of poorly soluble drugs
Oral Controlled-Release Solid Dosage Forms, Use of Novel Polymer and Unconventional Polymer Blends
Micro-valve technology for flexible processing of drug nanosuspensions into solid oral dosage forms
Predicting oral pharmacokinetic profiles of solid dosage forms containing poorly-soluble weak acid drugs
Hydrodynamics and solid dosage form disintegration/dissolution : immediate release tablets and novel in situ polyelectrolyte gastroretentive drug delivery systems
Combined assessment of dissolution and epithelial permeability of solid oral dosage forms
Phospholipids as functional excipients in solid oral dosage forms
“Solidified liquid lipids” for oral solid dosage forms : characterisation and processing
Biopredictive disintegration and dissolution of solid oral dosage forms : biorelevant in vitro tests for enteric-coated dosage forms and development of fast dissolving pH-responsive polymers
Evaluation of multiple factors influencing the ability to swallow solid oral dosage forms
Liposomes as a solid dosage form and for the oral delivery of vancomycin
Biorelevant dissolution test methods for modified release dosage forms
Development of discriminative and predictive dissolution tests for immediate release oral dosage forms of poorly soluble drugs
Oral Controlled-Release Solid Dosage Forms, Use of Novel Polymer and Unconventional Polymer Blends
Micro-valve technology for flexible processing of drug nanosuspensions into solid oral dosage forms
Predicting oral pharmacokinetic profiles of solid dosage forms containing poorly-soluble weak acid drugs
Hydrodynamics and solid dosage form disintegration/dissolution : immediate release tablets and novel in situ polyelectrolyte gastroretentive drug delivery systems
Combined assessment of dissolution and epithelial permeability of solid oral dosage forms
Phospholipids as functional excipients in solid oral dosage forms
“Solidified liquid lipids” for oral solid dosage forms : characterisation and processing
Biopredictive disintegration and dissolution of solid oral dosage forms : biorelevant in vitro tests for enteric-coated dosage forms and development of fast dissolving pH-responsive polymers
Evaluation of multiple factors influencing the ability to swallow solid oral dosage forms
Liposomes as a solid dosage form and for the oral delivery of vancomycin
Biorelevant dissolution test methods for modified release dosage forms
Development of discriminative and predictive dissolution tests for immediate release oral dosage forms of poorly soluble drugs
Oral Controlled-Release Solid Dosage Forms, Use of Novel Polymer and Unconventional Polymer Blends
Micro-valve technology for flexible processing of drug nanosuspensions into solid oral dosage forms
Predicting oral pharmacokinetic profiles of solid dosage forms containing poorly-soluble weak acid drugs