Dissolution Testing as a Prognostic Tool for Oral Drug Absorption: Immediate Release Dosage Forms

By J. Dressman, G. Amidon, C. Reppas, V. Shah. Pharmaceutical Research, 2004

1,113 citations recorded by the source corpus.

Subfields: Materials Chemistry, Molecular Biology, Pharmaceutical Science

View Paper: https://www.semanticscholar.org/paper/13fc3e138fc9842b099f51697cc690a6881525da

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

In Materials Chemistry

1. M. Brewster
2. Christopher J. H. Porter
3. W. Charman
4. S. Charman
5. H. Williams
6. R. Shanker
7. Natalie L. Trevaskis
8. T. Loftsson

In Molecular Biology

1. W. Charman
2. M. Brewster
3. Colin W. Pouton
4. Christopher J. H. Porter
5. S. Charman
6. H. Williams
7. R. Shanker
8. J. Emami

In Pharmaceutical Science

1. Christopher J. H. Porter
2. M. Brewster
3. W. Charman
4. Natalie L. Trevaskis
5. R. Shanker
6. S. Charman
7. H. Williams
8. Colin W. Pouton

Citations in the corpus

• In vitro - in vivo correlation: from theory to applications. (2006, methodology): “As the total volume of fluid entering the GI tract within 24 hrs period is only about 5 to 10 liters (16), insufficient fluid would be available at any given time to dissolve the entire dose of griseofulvin (7).”
• Nanosuspensions: a promising drug delivery strategy (2004, methodology): “According to the Nernst–Brunner and Levich modification of the Noyes Whitney dissolution model equation (Dressman et al 1998; Horter & Dressman 2001), the dissolution velocity of the nanosuspension increases due to a dramatic increase in the surface area of the drug particles from microns to…”
• Nanoparticle technology for drug delivery (2006, background): “716 ISBN 978-607-8164-02-8 where A is surface area, D is diffusivity, h is boundary layer thickness, Cs is saturation solubility, and Cb is bulk concentration (Dressman et al., 1998).”
• Strategies to Address Low Drug Solubility in Discovery and Development (2013, methodology): “Dispersion testing can be conducted in standard dissolution apparatus and using, for example, FaSSGF, FaSSIF, or FeSSIF media (Dressman et al., 1998; Dressman et al., 2007).”
• Cyclodextrins as pharmaceutical solubilizers. (2007, background): “The BCS divides drugs and drug candidates into 4 classes based on their solubility and permeability characteristics [52–54].”
• Pharmaceutical approaches to colon targeted drug delivery systems. (2003, background): “The GI residence time of the dosage forms is another important parameter for pH-dependent colon targeted drug delivery systems which is influenced by many physiological and other factors (78, 79); nevertheless, there are some generally accepted GI residence values for various parts of the GIT (80).”