Alliance iS Bio HPLC System - SPECIFICATIONS
Brochures and specifications | 2024 | WatersInstrumentation
The Alliance iS Bio HPLC System is critical for modern biopharmaceutical analysis, offering robust biocompatible flow paths and advanced automation to support the development and quality control of therapeutic proteins. By minimizing common errors and ensuring reliable performance, this system enhances productivity and compliance in bioanalytics.
This application note presents the design features, automation capabilities, and performance characteristics of the Alliance iS Bio HPLC System, a solution optimized for continuous and precise analysis of complex biotherapeutic samples.
The system integrates multiple modules:
Key specifications include:
The system’s biocompatible materials (MP35N, titanium, DLC) and integrated diagnostics deliver:
Emerging directions include integration with smart lab ecosystems, advanced column chemistries for high-resolution separations, and real-time monitoring with AI-driven data interpretation. The system can extend to multicompartment chromatography and automated process analytics in biomanufacturing.
The Alliance iS Bio HPLC System combines durable construction, precise control, and intelligent automation to support demanding biopharmaceutical analyses. Its comprehensive performance ensures accurate results, operational efficiency, and seamless integration into regulated laboratory environments.
HPLC
IndustriesOther
ManufacturerWaters
Summary
Significance of the Topic
The Alliance iS Bio HPLC System is critical for modern biopharmaceutical analysis, offering robust biocompatible flow paths and advanced automation to support the development and quality control of therapeutic proteins. By minimizing common errors and ensuring reliable performance, this system enhances productivity and compliance in bioanalytics.
Aim and Overview
This application note presents the design features, automation capabilities, and performance characteristics of the Alliance iS Bio HPLC System, a solution optimized for continuous and precise analysis of complex biotherapeutic samples.
Methodology and Instrumentation
The system integrates multiple modules:
- Quaternary Solvent Manager for four-solvent blending with vacuum degassing and low-pressure mixing
- Combined Conductive Heater and Cooler for single-column temperature control from 4 °C to 90 °C
- Tunable UV Detector covering 190–700 nm with deuterium lamp and patented Erbium filter
- Empower Chromatography Data System for instrument control and data management
Main Performance Highlights
Key specifications include:
- Total system dwell volume ≤1600 µL and gradient delay ≤1100 µL
- Flow rate range 0.001–10.000 mL/min with ±1.0% accuracy and ≤0.15% RSD
- Operating pressure up to 10 000 psi and full pH compatibility from 1 to 13
- Injection cycle time ≤30 seconds and unattended operation with leak detection
- Temperature accuracy ±0.5 °C and stability ±1 °C at the sensor
- Detector linearity r2 ≥0.999 and baseline noise <5 µAU
Benefits and Practical Applications
The system’s biocompatible materials (MP35N, titanium, DLC) and integrated diagnostics deliver:
- Enhanced method robustness for sensitive biomolecule separations
- Reduced downtime through automated leak management and priming
- Reproducible retention times via quantum synchronization
- Flexibility for gradient method development and high-throughput workflows
Future Trends and Potential Applications
Emerging directions include integration with smart lab ecosystems, advanced column chemistries for high-resolution separations, and real-time monitoring with AI-driven data interpretation. The system can extend to multicompartment chromatography and automated process analytics in biomanufacturing.
Conclusion
The Alliance iS Bio HPLC System combines durable construction, precise control, and intelligent automation to support demanding biopharmaceutical analyses. Its comprehensive performance ensures accurate results, operational efficiency, and seamless integration into regulated laboratory environments.
Reference
- All performance specifications are measured following a warm-up period of one hour. Ambient ∆T ≤±2.0 °C
- U.S. Patent Numbers: 6,423,249 and 6,783,705
- ASTM E1657-98, unless otherwise specified
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