Interest in minitablets (MTs) has grown exponentially over the last 20 years and especially
the last decade, as evidenced by the number of publications cited in Scopus and PubMed …

Bioavailability of oral drug formulations is strongly dependent on the composition of the
gastric and intestinal fluids and hydrodynamic conditions in the gastrointestinal tract. These …

Introduction Controlling the drug release from the dosage form at a definite rate is the main
challenge for a successful oral controlled-release drug delivery system. In this study, mini …

Chronic diseases like asthma, hypertension and rheumatoid arthritis requires prompt
release of drug as per the disease condition. Conversely, extended release systems can …

The aim of the current work was to develop generic sustained-release tablets containing 35
mg trimetazidine dihydrochloride and to establish an in vitro–in vivo correlation that could …

The solubility of glimepiride (GM) was improved from 1.6 μg/mL to 22.0 mg/mL when GM
and meglumine (MU) complexes were prepared. Therefore, transdermal hydrogels of GM …

Background The current research aims to determine the pharmacokinetic parameters,
mucoadhesive strength, and IVIVC correlation of the novel chronotherapeutic drug delivery …

IVIVC assessment, pharmacokinetic evaluation, and X-ray radiography mapping of novel
Parteck® SRP 80 and hypromellose-loaded LT Page 1 Jawed and Satish Future Journal of …

The current work aimed to formulate a modified pH independent/time controlled release
tablet for delayed drug delivery. The effect of different coating levels and polymer …

The preparation of minitablets from feed powder with a high micronized drug load is
generally unattainable via direct compression due to its inherent cohesivity, high charging …