Tablet Dissolution Test Apparatus
Measures the rate at which a dosage form releases its active ingredient into a medium.
Holds a dosage form in a heated, stirred medium and measures how much active is released over time. The apparatus type — rotating basket, paddle, reciprocating cylinder or flow-through cell — is set by the monograph, and the medium is held at 37 ± 0.5 °C throughout the run.
- Import, delivery and installation
- IQ/OQ and calibration by our Technical Services Division
- Genuine spares and operator training in Dhaka
Specifications
Specifications vary by model and configuration — the brochure carries the full range. Tell us your throughput, sample type and compliance requirement and we will confirm which model fits.
Download the brochure (PDF · 4 KB)Compliance & qualification
Dissolution is described in USP <711> and Ph. Eur. 2.9.3; apparatus suitability in USP <1092>.
Applications
Batch release of solid oral dosage forms, formulation and bioequivalence work, dissolution profile comparison, quality-by-design studies.
Also in Pharmaceutical Testing & Analytical Solutions