Results 21 to 30 of about 88,172 (307)

An In Vivo Predictive Dissolution Methodology (iPD Methodology) with a BCS Class IIb Drug Can Predict the In Vivo Bioequivalence Results: Etoricoxib Products

open access: yesPharmaceutics, 2021
The purpose of this study was to predict in vivo performance of three oral products of Etoricoxib (Arcoxia® as reference and two generic formulations in development) by conducting in vivo predictive dissolution with GIS (Gastro Intestinal Simulator) and ...
Isabel Gonzalez-Alvarez   +8 more
doaj   +1 more source

Dissolution of gallstones in vitro

open access: yesKazan medical journal, 1995
With the help of ultrasound and NMR tomography, the diagnosis of stones in the biliary tract has improved significantly. In this regard, the number of patients who want to get rid of stones, the existence of which they did not even suspect before the examination, is growing significantly.
R. A. Zulkarneev   +2 more
openaire   +1 more source

Drug release from matrix tablets: physiological parameters and the effect of food [PDF]

open access: yes, 2014
Introduction: As dissolution plays an important and vital role in the drug-delivery process of oral solid dosage forms, it is, therefore, essential to critically evaluate the parameters that can affect this process. Areas covered: The consumption of
Ali Nokhodchi   +5 more
core   +1 more source

Interaction of naproxen with calcium carbonate: physicochemical characterization and in vitro drug release studies

open access: yesQuímica Nova, 2014
Interaction and physicochemical characterization of dispersions of naproxen in calcium carbonate after freeze-drying the wet-state equilibrated mixture have been investigated by analytical methods.
Shweta Paroha   +2 more
doaj   +1 more source

In vivo dissolution of poorly water-soluble drugs: Proof of concept based on fluorescence bioimaging

open access: yesActa Pharmaceutica Sinica B, 2021
In vitro‒in vivo correlation (IVIVC) of solid dosage forms should be established basically between in vitro and in vivo dissolution of active pharmaceutical ingredients. Nevertheless, in vivo dissolution profiles have never been accurately portrayed. The
Yinqian Yang   +9 more
doaj   +1 more source

Dissolution Stability Study of Cefadroxil Extemporaneous Suspensions [PDF]

open access: yes, 2008
Dissolution studies have become matter of great significance because, in most cases, drug dissolution is the rate-limiting step in the absorption process.
Noelia L. Gonzalez Vidal   +8 more
core   +1 more source

Poly(alkyl methacrylate) tooth coatings for dental care: evaluation of the demineralisation-protection benefit using a time-resolved in vitro method [PDF]

open access: yes, 2011
An in vitro method for the time-resolved quantification of acid-mediated tooth demineralisation has been developed and evaluated against putative non-permanent protective formulations based on a series of poly(alkyl methacrylate)s.
Birthe V. Nielsen   +16 more
core   +1 more source

Evaluation of lipid-based formulations of poorly water-soluble drugs in the gastro-intestinal tract using in vitro tests [PDF]

open access: yes, 2011
Novel active pharmaceutical ingredients are often poorly water-soluble. Such compounds may only partially dissolve or may precipitate during intestinal passage, potentially leading to incomplete drug absorption. Despite the importance of the process, the
Arnold, Yvonne Elisabeth
core   +1 more source

Improvement in vitro Dissolution Rate of Quercetin Using Cocrystallization of Quercetin-Malonic Acid

open access: yesIndonesian Journal of Chemistry, 2018
The aim of the study was to improve the in-vitro dissolution rate of quercetin (Qu) using cocrystallization of quercetin. Cocrystals of quercetin (Co Qu) were produced with malonic acid (Ma) as coformer at ratio 1:2 using solvent evaporation method ...
Dwi Setyawan   +3 more
doaj   +1 more source

A study on the influence of the dissolution test factors on in vitro release of ibuprofen from sustained release tablets [PDF]

open access: yesRomanian Journal of Pharmaceutical Practice, 2020
Objectives. The aim of this study was to investigate the influence of in vitro release test parameters on the release of ibuprofen from sustained release inert matrix tablets. Materials and methods.
Alexandra Pali   +4 more
doaj   +1 more source

Home - About - Disclaimer - Privacy