Sodium Starch Glycolate

Stability is an essential quality attribute of any pharmaceutical formulation. Poor stability can change the color and physical appearance of...

Bilayer/multilayer tablets have been introduced to formulate incompatible components for compound preparations, but they are now more commonly used to...

Aim of this study was to develop a tablet formulation for targeted colonic drug release by implementing two control mechanisms:...

Tablet disintegration is an important pre-requisite for drug dissolution and absorption. The disintegration test is typically conducted at 37 °C,...

Orally disintegrating tablets are an emerging trend in novel drug delivery system and have received ever increasing demand during the...

The time taken by the tablet to break down into fragments or granules is called disintegration. The time it takes...

This study demonstrated the implementation of a liquisolid technique to formulate directly compressible orally disintegrating tablets (ODTs). Cannabidiol (CBD), a...

Abstract The disintegration time is critical for characterizing orally disintegrating tablets (ODTs), according to regulatory standards. The current study aimed...

According to the Quality by Design (QbD) concept, Design of Experiment (DoE) was used to indicate critical process parameters and...

Colonic targeting of orally applied therapeutic drugs remains a challenge. Tablet coatings relying on gastrointestinal pH and colonic bacterial enzymes as triggers...