Dissolution Testing USP 1/2/5/6

Dissolution tests are used in the pharmaceutical industry in order to characterize the dissolution properties of the active drug, the active drug's release, as well as the dissolution from a dosage formulation. Different dissolution testing methods are available in USP, Ph.Eur., and other internationally harmonized Pharmacopeia. While standard tablets are typically tested using the paddle method (USP 2), swelling or floating dosage forms e.g. capsules are tested according to the basket method (USP 1), whereas paddle-over-disk (USP 5) and rotating cylinder (USP 6) methods are utilized for transdermal dosage forms.

Fully-Automated Dissolution Testers

If your laboratory team spends much of their time on tasks such as filling vessels and cleaning, SOTAX's automation for dissolution testing might be an ideal solution - it allows qualified staff to focus on critical tasks rather than sup...

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Semi-Automated Dissolution Testers

SOTAX's semi-automated dissolution testers enable automated sampling with identical withdrawal positions and thus ensure repeatability. In addition, they allow for fast sampling timepoints pushing through fine filtration even when using ...

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Manual Dissolution Testers

SOTAX's manual dissolution testers make manual sampling processes simple and repeatable.

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