Oral administration of a drug substance has become one of the most important drug delivery
routes. In chronic diseases such as rheumatoid arthritis or osteoarthritis, oral forms of drugs …

Cocrystals that are more soluble than the constituent drug, generate supersaturation levels
during dissolution and are predisposed to conversion to the less soluble drug. Drug release …

Piroxicam (PRM) and meloxicam (MEL) are two nonsteroidal anti-inflammatory drugs,
belonging to the Biopharmaceutics Classification System Class II drugs. In this study, six …

Fast dissolution of nonsteroidal anti-inflammatory drugs (NSAIDs) is a prerequisite from
patient perspective. However, most NSAIDs are slowly dissolving acidic compounds …

A biopharmaceutics classification system class IV drug, hydrochlorothiazide (HCT), was
combined with co-formers of L-and d-arginine (ARG) and sodium lauryl sulphate (SLS) by …

Co-amorphous systems are an attractive alternative for amorphous solid polymer
dispersions in the formulation of poorly soluble drugs. Several studies have revealed that co …

The objective of this work was to prepare and evaluate fast dissolving sublingual films
containing meloxicam nanocrystals (MLX-NS-FDSFs). Nanocrystals (NS) were utilized to …

The oral dosage route still remains the most common and preferred route for drug
administration due to convenient handling, high patient compliance, and cost-effectiveness …

Meloxicam (MEL) shows a slow onset of action in severe pain patients on account of
delayed gastric motility. This study aimed to develop an amorphous solid dispersion (ASD) …

The aim of this research is the development of new colonic release systems of meloxicam
(MLX) a non-steroidal anti-inflammatory drug (NSAIDs) with pH and time-dependent …