In vivo methods for drug absorption–comparative physiologies, model selection, correlations with in vitro methods (IVIVC), and applications for formulation/API …

E Sjögren, B Abrahamsson, P Augustijns… - European Journal of …, 2014 - Elsevier
This review summarizes the current knowledge on anatomy and physiology of the human
gastrointestinal tract in comparison with that of common laboratory animals (dog, pig, rat and …

Hydrogel delivery systems for vaginal and oral applications: Formulation and biological considerations

K Knuth, M Amiji, JR Robinson - Advanced drug delivery reviews, 1993 - Elsevier
Hydrophilic polymer gels (hydrogels) exhibit a range of physical, chemical, and biological
properties which makes them attractive as drug delivery systems. Such systems are …

[图书][B] Handbook of pharmaceutical controlled release technology

DL Wise - 2000 - taylorfrancis.com
The Handbook of Pharmaceutical Controlled Release Technology reviews the design,
fabrication, methodology, administration, and classifications of various drug delivery …

The influence of variable gastric emptying and intestinal transit rates on the plasma level curve of cimetidine; an explanation for the double peak phenomenon

RL Oberle, GL Amidon - Journal of pharmacokinetics and …, 1987 - Springer
A physiological flow model is presented to account for plasma level double peaks based on
cyclical gastric emptying and intestinal motility in the fasted state. Central to the model is the …

Relative bioavailability estimation of carbamazepine crystal forms using an artificial stomach-duodenum model

SR Carino, DC Sperry, M Hawley - Journal of pharmaceutical sciences, 2006 - Elsevier
The in vitro dissolution of carbamazepine (CBZ) was investigated using an automated
artificial stomach-duodenum (ASD) model. Successful simulation of the dog physiology in …

Novel High-Drug-Loaded Amorphous Dispersion Tablets of Posaconazole; In Vivo and In Vitro Assessment

DM Mudie, AM Stewart, N Biswas… - Molecular …, 2020 - ACS Publications
Amorphous solid dispersions (ASDs) can increase the bioavailability of drugs with poor
aqueous solubility. However, concentration-sustaining dispersion polymers (CSPs) …

Oral controlled-release delivery

PK Gupta, JR Robinson - Treatise on controlled drug delivery, 2017 - taylorfrancis.com
This chapter reviews oral controlled-release (CR) systems, with a focus on dosage-form
characteristics and gastrointestinal (GI) physiology. Since an understanding of the basic …

A new multiple-unit oral floating dosage system. II: In vivo evaluation of floating and sustained-release characteristics with p-aminobenzoic acid and isosorbide …

M Ichikawa, T Kato, M Kawahara, S Watanabe… - Journal of …, 1991 - Elsevier
In a previous study, we developed a multiple-unit type of oral floating dosage system, which
is a new type of floating pill composed of both an effervescent layer and a swellable …

Companion animal physiology and dosage form performance

SC Sutton - Advanced drug delivery reviews, 2004 - Elsevier
Among the most critical parameters for any drug candidate are tolerability, dose, solubility
and permeability. For controlled release formulations, gastrointestinal transit is an added …

Dissolution media simulating the proximal canine gastrointestinal tract in the fasted state

M Arndt, H Chokshi, K Tang, NJ Parrott… - European Journal of …, 2013 - Elsevier
Human biorelevant media have been shown to be a useful tool in pharmaceutical
development and to provide input for in silico prediction of pharmacokinetic profiles after oral …