Results 351 to 360 of about 11,911,230 (418)
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Expandable gastroretentive dosage forms

Journal of Controlled Release, 2003
Expandable gastroretentive dosage forms (GRDFs) have been designed for the past 3 decades. They were originally created for possible veterinary use, but later the design was modified for enhanced drug therapy in humans. These GRDFs are easily swallowed and reach a significantly larger size in the stomach due to swelling or unfolding processes that ...
Eytan Klausner   +3 more
openaire   +2 more sources

Evaluation of Dosage Forms. IV. Studies on Commercial Phenylbutazone Tablet Dosage Forms

Drug Development and Industrial Pharmacy, 1998
In order to determine the feasibility of dissolution-dialysis as a suitable technique for in vitro evaluation, studies on commercial phenylbutazone tablets were carried out. Although disintegration time and dissolution parameters did not give a true indication of bioavailability, an excellent correlation was obtained between the dialysis rate constant (
Balkishen Razdan, Anant Paradkar
openaire   +3 more sources

Electrospinning and its potential in fabricating pharmaceutical dosage form

Journal of Drug Delivery Science and Technology, 2022
Siew Mei Tan   +7 more
semanticscholar   +1 more source

Effect of surfactants, gastric emptying, and dosage form on supersaturation of dipyridamole in an in vitro model simulating the stomach and duodenum.

Molecular Pharmaceutics, 2014
The purpose of this study was to investigate the influence of gastric emptying patterns, surfactants, and dosage form on the supersaturation of a poorly soluble weakly basic drug, dipyridamole, using an in vitro model mimicking the dynamic environment of
A. Mitra, H. Fadda
semanticscholar   +1 more source

Evaluation of Dosage Forms. VI. Studies of Commercial Oxyphenbutazone Tablet Dosage Forms

Drug Development and Industrial Pharmacy, 1999
Dissolution-dialysis studies of commercial tablets of oxyphenbutazone were carried out to establish the applicability of this technique for the in vitro evaluation of oxyphenbutazone dosage form. While disintegration time and dissolution rate studies did not give a true indication of bioavailability, an excellent correlation was obtained between the ...
Balkishen Razdan, N. V. Nagaraj
openaire   +3 more sources

Pharmaceutical application and development of fixed-dose combination: dosage form review

Journal of Pharmaceutical Investigation, 2021
Dong-Wook Kim, Kwon-Yeon Weon
semanticscholar   +1 more source

Pharmaceutical Dosage Forms

1979
Pharmaceutical aerosols are packaged under pressure and contain therapeutically active ingredients. They are intended for topical application to the skin as well as local application, including inhalation.
W. T. Lowry, James C. Garriott
openaire   +2 more sources

Disintegrants in Solid Dosage Forms

Drug Development and Industrial Pharmacy, 1990
AbstractThe dynamic approach to tablet disintegration, which is based on the measurement of the force that develops inside the compact upon water entrance, is basically taken up.The combined measurements of force development and water uptake, simultaneously effected on the same compact, provide a novel parameter that is proposed to quantify and compare
CARAMELLA, CARLA MARCELLA   +3 more
openaire   +2 more sources

Assessment of Dosage Forms In Vitro

1988
This chapter presents descriptions of some in vitro tests which can be applied to pharmaceutical products, using some of the background physical chemistry discussed in other chapters. In particular, we will examine the influence of some of the key parameters of pharmaceutical systems, such as particle size, viscosity, adhesion or formulation in general
D. Attwood, A. T. Florence
openaire   +2 more sources

An Overview of Pharmaceutical Process Validation of Solid Dosage Form.

, 2013
The present article gives an introduction and general overview on process validation of pharmaceutical manufacturing process especially tablet manufacturing process.
Umed A. Nikam   +3 more
semanticscholar   +1 more source

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