Pharmaceutical dissolution testing for solid oral dosage forms is a complex analytical procedure where the control of critical variables (environmental conditions, equipment performance, sample ...

As interest in essential oils (EOs) for their therapeutic, antibacterial, and antifungal properties continues to grow—driving demand for high-quality products in both medicinal and industrial ...

The proteins that make up our cells hold within an entire world of information, which, when unlocked, can give us insights into the origins of many essential biological phenomena. This information is ...

As the pace of product development accelerates, the approach to dissolution-method development must advance beyond a manual method and an assay. A natural progression of the method-development process ...

Agilent Technologies Inc. introduced SampliQ QuEChERS kits that simplify sample preparation for analyzing pesticide residues in fruits, vegetables and processed food products. “QuEChERS,” developed by ...

Validating the match between the active ingredient content mentioned in the packaging and the actual content in each tablet in a batch is a critical step in tablet manufacture. Highly precise ...

Chromite is an iron chromium oxide mineral (FeCr 2 O 4), which is a source of commercial importance. It contains 68% of chromic oxide (Cr 2 O 3), wherein the proportions of Fe 2+, Fe 3+, Mg 2+, Cr 3+ ...

Particle morphology of magnesium stearate, added as an anti-caking agent in a high water‑soluble drug substance, has an influence on the dissolution rate of compressed tablets. Magnesium stearate ...

Single-cell proteomics provides information about a cell at its protein level, which can prove useful for anticancer drug resistance and cell differentiation research. However, current proteomics ...