Results 171 to 180 of about 1,723 (196)
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Developing a Biorelevant Dissolution Method for an Extrudable Core System (ECS) Osmotic Tablet
AAPS PharmSciTech, 2021The objective of this work is to develop a biorelevant dissolution method to support the clinical study for In Vitro In Vivo Correlation (IVIVC) of the first commercially approved single-layer extrudable core system (ECS) osmotic tablet - the 11 mg tofacitinib modified-release tablet.
Raymond, Chen +5 more
openaire +2 more sources
International Journal of Pharmaceutics, 2021
Amorphous Solid Dispersions (ASDs) are a major drug formulation technique to achieve higher bioavailability for poorly water-soluble active pharmaceutical ingredients. So far, dissolution tailoring and supersaturation enhancement have been studied in detail, whereas less is known about the importance of formed precipitates with amorphous or crystalline
Martin, Müller +7 more
openaire +2 more sources
Amorphous Solid Dispersions (ASDs) are a major drug formulation technique to achieve higher bioavailability for poorly water-soluble active pharmaceutical ingredients. So far, dissolution tailoring and supersaturation enhancement have been studied in detail, whereas less is known about the importance of formed precipitates with amorphous or crystalline
Martin, Müller +7 more
openaire +2 more sources
International Journal of Pharmaceutics, 2021
Currently, there is no compendial-level method to assess dissolution of particulate systems administered in the periodontal pocket. This work seeks to develop dissolution methods for extended release poly(lactic-co-glycolic acid) (PLGA) microspheres applied in the periodontal pocket. Arestin®, PLGA microspheres containing minocycline hydrochloride (MIN)
Sravan Kumar Patel +11 more
openaire +2 more sources
Currently, there is no compendial-level method to assess dissolution of particulate systems administered in the periodontal pocket. This work seeks to develop dissolution methods for extended release poly(lactic-co-glycolic acid) (PLGA) microspheres applied in the periodontal pocket. Arestin®, PLGA microspheres containing minocycline hydrochloride (MIN)
Sravan Kumar Patel +11 more
openaire +2 more sources
Use of biorelevant dissolution and PBPK modeling to predict oral drug absorption
European Journal of Pharmaceutics and Biopharmaceutics, 2018Compromised oral drug absorption, due to poor aqueous solubility, is one of the major challenges faced by the pharmaceutical industry in the drug discovery and development process. Scientific community is striving to develop tools for accurate prediction of the oral absorption profile of drugs.
Navpreet, Kaur +2 more
openaire +2 more sources
Theoretical Dissolution Model of Poly-Disperse Drug Particles in Biorelevant Media
Journal of Pharmaceutical Sciences, 2008The purpose of the present study was to construct the theoretical dissolution model of poly-disperse drug particles in biorelevant media containing bile salt/ lecithin aggregates (micelles or vesicles). The effective diffusion coefficient in the biorelevant medium and the particle size distribution of drug particles were simultaneously factored into ...
Arimichi, Okazaki +2 more
openaire +2 more sources
AAPS PharmSciTech, 2020
Poorly soluble weak bases form a significant proportion of the drugs available in the market thereby making it imperative to understand their absorption behavior. This work aims to mechanistically understand the oral absorption behavior for a weakly basic drug, Irbesartan (IRB), by investigating its pH dependent solubility, supersaturation, and ...
Navpreet, Kaur +5 more
openaire +2 more sources
Poorly soluble weak bases form a significant proportion of the drugs available in the market thereby making it imperative to understand their absorption behavior. This work aims to mechanistically understand the oral absorption behavior for a weakly basic drug, Irbesartan (IRB), by investigating its pH dependent solubility, supersaturation, and ...
Navpreet, Kaur +5 more
openaire +2 more sources
Molecular Pharmaceutics, 2013
Intragastric drug release from solid oral dosage forms can be affected by altered physicochemical and mechanical conditions in the upper gastrointestinal (GI) tract. Food effects may lead to changes of one or more pharmacokinetic parameters and, hence, influence drug plasma levels.
Mirko, Koziolek +3 more
openaire +2 more sources
Intragastric drug release from solid oral dosage forms can be affected by altered physicochemical and mechanical conditions in the upper gastrointestinal (GI) tract. Food effects may lead to changes of one or more pharmacokinetic parameters and, hence, influence drug plasma levels.
Mirko, Koziolek +3 more
openaire +2 more sources
Molecular Pharmaceutics, 2018
Biorelevant dissolution media (BDM) methods are commonly employed to investigate the oral absorption of poorly water-soluble drugs. Despite the significant progress in this area, the effect of commonly employed pharmaceutical excipients, such as surfactants, on the solubility of drugs in BDM has not been characterized in detail.
Zahari Vinarov +4 more
openaire +2 more sources
Biorelevant dissolution media (BDM) methods are commonly employed to investigate the oral absorption of poorly water-soluble drugs. Despite the significant progress in this area, the effect of commonly employed pharmaceutical excipients, such as surfactants, on the solubility of drugs in BDM has not been characterized in detail.
Zahari Vinarov +4 more
openaire +2 more sources
Biorelevant dissolution testing of colon-specific delivery systems activated by colonic microflora
Journal of Controlled Release, 2008The fermentation of non-starch polysaccharides by colonic microflora is popular as a triggering mechanism to achieve colon-specific drug delivery in that the existence of colonic microflora is independent of gastrointestinal transit time, pH, and disease conditions, and various delivery systems were developed using this strategy.
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Evaluation of biorelevant dissolution media simulating fasted and fed states
2018The most important criteria for evaluating in vitro performance and in vivo behavior of drugs is dissolution tests. It is necessary to provide conditions that best mimic the in vivo media in dissolution tests. The most important condition is the dissolution media used.
Yaşin, Diren Sarısaltık +1 more
openaire +1 more source

