The objective of this work was to access thymol-excipient compatibility using an alternative
protocol of mixture design subsidizing the development of nanostructures lipid carriers …

The aim of our research was to develop a miniaturized high throughput drug-excipient
compatibility test. Experiments were planned and evaluated using statistical experimental …

This mini-review discusses the importance of thermal analysis as a predictive tool for
pharmaceutical stability in the design of drug-excipient compatibility studies. In this regard …

Estimation of drug–excipient interactions is a crucial step in preformulation studies of drug
development to achieve consistent stability, bioavailability and manufacturability of solid …

The safety, efficacy, quality and stability of a formulation are the cornerstones of any new
drug development process. In order to consistently maintain these attributes in a finished …

Pharmaceutical excipients are traditionally considered as pharmacologically inert
substances, but, can also actively participate in drug–excipient interactions, viz., physical …

The stability of pharmaceuticals is an important product quality attribute. Of the known factors
affecting stability, moisture is often perceived as the most common cause of drug …

Lipoic acid is derived from octanoic acid and is considered a universal antioxidant for
combating free radicals and regeneration of endogenous antioxidant, as well as acting like …

Drug-excipient compatibility study (DECS) is one of the critical steps during pre-formulation
studies to select the appropriate excipient to obtain a stable formulation/dosage form. As …

Studies of active pharmaceutical ingredient (API)-excipient compatibility represent an
important study in the preformulation stage of the development of new dosage forms. The …