Analytical data from drug dissolution testing are sufficient in many cases to establish safety and efficacy of a drug product without in vivo tests, following minor formulation and manufacturing changes …

Dissolution is the process in which a substance forms a solution. Dissolution testing measures the extent and rate of solution formation from a dosage form, such as tablet, capsule, ointment, etc. The …

May 1, 2025 · Dissolution testing evaluates the rate and extent to which an active pharmaceutical ingredient (API) is released from a solid oral dosage form—such as a tablet or capsule—into a liquid …

Dissolution testing is a standardized laboratory method in the pharmaceutical industry that measures the rate and extent a solid dosage form, such as a tablet or capsule, turns into a solution.

Agilent supplies a range of dissolution instrumentation for release-rate testing. Our dissolution testers are compliant with harmonized USP, EP, and JP testing criteria. In general, our dissolution portfolio …

Oct 2, 2019 · In this article, experts discuss the fundamentals of dissolution testing and highlight the challenges that are surfacing as a result of the increasing numbers of poorly soluble molecules …

Dissolution testing is a fundamental analytical technique in the pharmaceutical industry, providing information on how a drug is released from its dosage form. This analysis is vital for ensuring product …

Feb 28, 2024 · Dissolution testing - exploring the ‘why, how and what’ of this core analytical technique for oral solid dosage forms.

Dec 17, 2024 · Learn how to perform dissolution testing for pharmaceuticals, ensuring accurate drug release and compliance with industry standards

Mar 10, 2025 · The Dissolution test is an important quality control (QC) procedure used in the pharmaceutical industry to evaluate the release rate of the active pharmaceutical ingredient (API) …