The DS-1206AT auto sampling dissolution system is a high-performance 12-cup and 12-rod dissolution testing device designed and manufactured in accordance with the requirements of the 2020 edition of the Chinese Pharmacopoeia, the US Pharmacopoeia, and the Guiding Principles for Mechanical Validation of Drug Dissolution Meters.
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Overview
An automated dissolution testing instrument designed for pharmaceutical quality control, featuring a stainless steel construction compliant with USP/EP standards. This system integrates precise temperature regulation and synchronized sampling mechanisms to ensure accurate drug release profiles.
Application
- Pharmaceutical Manufacturing: Routine quality assurance for solid oral dosage forms.
- R&D Laboratories: Formulation development and bioequivalence studies.
- Contract Testing Services: Third-party verification of generic drug specifications.
Precautions
- Maintain strict sterility protocols to prevent cross-contamination between batches.
- Schedule regular calibration of motor speed and thermal sensors per ISO guidelines.
- Replace wear-prone components like stirrer shafts and seals annually or after specific cycle counts.