Dissolution & Drug-Excipient Studies
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Dissolution & Drug-Excipient Studies
Dissolution testing measures the rate and extent to which the active pharmaceutical ingredient (API) is released from a solid dosage form (like tablets or capsules) into solution. It serves as a critical quality control and predictive tool for bioavailability and therapeutic efficacy.
Why choose?
Latest equipment
Testing equipment have significantly enhanced efficiency.
Safe diagnoses
Both accurate results and lab personnel/environmental safety.
Key Points
- Evaluate drug release characteristics.
- Ensure batch-to-batch consistency.
- Support formulation development and process optimization.
- Establish in-vitro/in-vivo correlation (IVIVC).
Common Dissolution Apparatus (USP)
- Apparatus 1 (Basket)
- Apparatus 2 (Paddle)
- Apparatus 3 (Reciprocating Cylinder)
- Apparatus 4 (Flow-through Cell)
