Dissolution Tester with Automated Sampling USP Apparatus 3

The DISSO-3 reciprocating cylinder apparatus is a valuable tool for evaluating API release characteristics for sustained-release, enteric, soft capsules, chewable tablets, or any solid dosage form where evaluation of different pH conditions is important.

Features

• Available in 6-row or 12-row configurations
• 300 mL or 1 L vessel options
  • 300 mL: eight sample holders x six rows
  • 1 L: eight sample holders with eight 1 L positions
• Unique anti-evaporation vessel cover significantly reduces solvent evaporation and prevents cross contamination
• Ability to configure multi-point sampling per row for dissolution method screening
• Programmable stroke distance to ensure USP compliance with different dosage types
• Multiple mesh screen sizes and materials to choose from
• Automated media replacement to ensure sink conditions
• Post-test wash routines
• Storage up to 20 methods
• Administrator, manager, operator security levels
• 21 CFR Part 11, USP, EP, JP, CP compliant

Dissolution Release Rate Tester Using USP Apparatus 3

Extended Functions

• Available camera monitoring system can record the entire process of drug release
• Compatible with the Logan Permetro bioequivalence (BE) tester
• Ability to run with on-line UV

Application

• USP Apparatus 3 is commonly used for testing of drugs such as sustained-release, enteric-coated, soft capsules, and chewable tablets.