Orally disintegrating tablets (ODTs) rapidly disintegrate or dissolve in the oral cavity without
using water. Demand for ODTs has increased, and the field has overgrown in the …

Cyclodextrins (CDs) have been widely investigated as a unique pharmaceutical excipient for
past few decades and is still explored for new applications. They are highly versatile …

Orally disintegrating tablets (ODTs), also known as fast melts, quick melts, fast disintegrating
and orodispersible systems, have the unique property of disintegrating in the mouth in …

Many drug candidates are poorly water-soluble. Microenvironmental pH (pHM) modification
in buccal/sublingual dosage forms has attracted increasing interest as a promising …

The aim ofthis study was to evaluate the influence of disintegration mechanism ofvarious
types of disintegrants on the absorption ratio (AR), Wetting time (WT), and disintegration time …

Being a biopharmaceutics classification system class II drug, the absorption of sertraline
from the gut is mainly limited by its poor aqueous solubility. The objective of this …

Niosomes suggest a versatile vesicle delivery system with possible transport of drugs via
topical route for skin delivery. The aim of the present research was to optimize niosome gel …

Oral therapy of tramadol, an opiate analgesic, undergoes extensive hepatic metabolism and
requires frequent administration. Transdermal therapy by virtue can overcome these issues …

Introduction: Orally disintegrating tablets (ODTs) have emerged as one of the novel solid
oral dosage forms with a potential to deliver a wide range of drug candidates to both …

Therapeutic efficacy of antifibrotic drugs can be improved by targeting hepatic stellate cells
(HSCs). This study investigated the prospect of develo** a carrier system for the effective …