JRS Pharma

Disintegration is the first event in the bioavailability cascade after the ingestion of immediate release tablets. Although the influence of...

When one wishes to convert a batch based manufacturing process of an existing tablet product to a continuous process, there...

Oral drug delivery systems for time-controlled release, intended for chronotherapy or colon targeting, are often in the form of coated...

This work proposes the design of novel oral disintegrating tablets (ODTs) of loperamide HCl with special emphasis on disintegration and...

The compaction of multiple unit-pellet system (MUPS) tablets poses considerable challenges due to potential compaction-induced damage to the functional polymer...

Fast disintegrating tablets have commonly been used for fast oral drug delivery to patients with swallowing difficulties. The different characteristics...

A simple paper-based microfluidic device, fabricated on a highly porous coating consisting of functionalised calcium carbonate (FCC) pigment and a...

The aim of this research was to simulate oral pharmacokinetic (PK) profiles of atorvastatin from orally disintegrating tablets (ODTs) dosed...

Microneedles are emerging drug delivery methods for painless treatment. The current study tested dissolving microneedles containing lidocaine (Li-DMN) for use...

How the evolution from traditional powdered cellulose to microcrystalline cellulose to a new generation of co processed high functionality excipients...