Lipid-based emulsion system—a subcategory of emulsion technology, has emerged as an
enticing option to improve the solubility of the steadily rising water-insoluble candidates …

The demands on the functionality of excipients are increasing day by day because of the
emergence of high-speed tableting machines and the use of direct compression methods for …

Pirfenidone (PFD) is the first pharmacological agent approved by the US Food and Drug
Administration (FDA) in 2014 for the treatment of idiopathic pulmonary fibrosis (IPF). The …

One of the most common forms of controlled release technology for oral drug delivery
comprises an active ingredient dispersed in a hydrophilic matrix forming polymer such as …

Active pharmaceutical ingredients (APIs) and excipients can be carefully combined in
premix-based materials before being added to dosage forms, providing a flexible platform …

Introduction As a nature-derived polymer with swelling and gelling properties, alginate has
found wide biopharma-relevant applications. However, there is comparatively limited …

Disintegration is the process where tablets break down into small particles in a liquid
medium. Sufficient disintegration of tablets is conducive to the rapid dissolution of drugs and …

Background/Objectives: Hydroxypropyl methylcellulose (HPMC) is one of the most
commonly used hydrophilic polymers in formulations of matrix tablets for controlled release …

Since famotidine (FA) is prescribed for gastrointestinal diseases orodispersible tablets could
contribute to patients' compliance. Its bitter taste and poor compressibility pose formulation …

With the advent of continuous manufacturing, twin-screw melt granulation has attracted
interest in the pharmaceutical industry as a method for co-processing excipients and …