PTWS 1230 Dissolution Testing System
The PTWS 1230 is a high-capacity dissolution testing system designed for pharmaceutical laboratories requiring maximum throughput and operational efficiency. Equipped with 12 testing positions, the instrument enables simultaneous testing of multiple samples, making it particularly suitable for biowaiver studies, formulation development, comparative dissolution testing, and high-volume quality control applications.
Built on Pharma Test’s proven MonoShaft™ technology, the PTWS 1230 delivers accurate, reliable, and reproducible dissolution testing while ensuring full compliance with USP, EP, BP, DAB, and JP pharmacopeia standards. In addition to its 12 dissolution vessels, the system incorporates two auxiliary vessels for standard or blank solutions, providing added flexibility for method validation and analytical workflows.
Featuring a modern touchscreen interface, advanced method management, comprehensive audit trail functionality, and user administration controls, the PTWS 1230 supports data integrity requirements and regulatory compliance. Its combination of high sample capacity, precision performance, and flexible operation makes it an ideal solution for pharmaceutical manufacturers, CROs, and research laboratories seeking enhanced productivity and testing efficiency.
Built on Pharma Test’s proven MonoShaft™ technology, the PTWS 1230 delivers accurate, reliable, and reproducible dissolution testing while ensuring full compliance with USP, EP, BP, DAB, and JP pharmacopeia standards. In addition to its 12 dissolution vessels, the system incorporates two auxiliary vessels for standard or blank solutions, providing added flexibility for method validation and analytical workflows.
Featuring a modern touchscreen interface, advanced method management, comprehensive audit trail functionality, and user administration controls, the PTWS 1230 supports data integrity requirements and regulatory compliance. Its combination of high sample capacity, precision performance, and flexible operation makes it an ideal solution for pharmaceutical manufacturers, CROs, and research laboratories seeking enhanced productivity and testing efficiency.
Features
- Fully USP <711/724>, EP <2.9.3/4>, BP, DAB and JP <15> compliant
- 12 stirred positions in a 6 + 6 arrangement, 2 extra vessels for refilling or standard media
- Electronic lifter for instrument head with 16 programmable working positions
- Low-evaporation vessel covers with silicone inlay
- Staggered start capability for all testing stations
- Programmable infinity test
- Method management and user administration
- Audit trail recording all events and changes with before and after information
Applications
- Biowaiver Studies
- Pharmaceutical Quality Control
- Comparative Dissolution Testing
- Formulation Development
- Generic Drug Development
- Stability Studies
- Method Validation
- Contract Research and Testing Laboratories
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SPECIFICATIONS
SPECIFICATIONS
- Stirrer speed range: 25 – 250 RPM
- Stirrer speed accuracy: ±2% of set speed, typically < 1%
- Stirrer shaft wobble: Better than 0.2 mm total run out
- Heating system: Heating and circulation pump module
- Heating range: 25.0 – 45.0°C
- Heating accuracy: ± 0.2°C inside the water bath
- Display & date entry: 7 inch display, 1024×600 pixel resolution color LCD touch screen,
- Audit trail: Integrated, logging all events and changes with before and after
- User management: Unlimited number of users with password and user rights
- Sampling positions: 16 programmable sampling probe immersion positions
- Method management: Unlimited number of methods
TABLET DISSOLUTION TESTING