Polyethylene Glycol (PEG)

Bioavailability, one of the prime pharmacokinetic properties of a drug, is defined as the fraction of an administered dose of...

To improve the dissolution and oral bioavailability of valsartan (VST), we previously formulated a supersaturable self-microemulsifying drug delivery system (SuSMED)...

The present study explores the effect of melt binding of Soluplus® on in vitro release profiles of two hydrophilic drugs,...

Implication of Quantitative Selection of Each Excipient in Product Development Excipients’ role in designing different dosage forms does not require...

Most microbial infectious diseases can be treated successfully with the remarkable array of antimicrobials current available; however, antimicrobial resistance, adverse...

Hydroxypropyl methylcellulose (HPMC) is one of the most important hydrophilic ingredients used in hydrogel matrices preparation (tablets or granules). In...

Objectives: We aimed to examine the administration of eight potentially harmful excipients of interest (EOI), including paraben, polysorbate 80, propylene...

In spite of the large research efforts in the past two decades, it is still difficult, if possible at all,...

Hydrophobic and hydrophilic thermoplastic poly(urethane) (TPU) mixtures offer the opportunity to tune water swelling capacity and diffusion rate for drugs...

Flowability is a key consideration during the formulation and process development of oral solid dosage forms as it can have...