Cytiva Sweden AB - Akta ready™ Chromatography System

• Biopharmaceutical manufacturing, particularly for monoclonal antibodies and recombinant proteins.
• Viral vector and nucleic acid purification in gene therapy and vaccine production.
• Process scale-up and development for bioprocesses.
• GMP-regulated production of sensitive therapeutic products.
• Small-batch purification through to larger process requirements in bioprocessing.

Typical flow rate range

For this class of equipment, flow rates commonly range from millilitres per minute up to several litres per minute, depending on the specific flow kit installed.

Operating pressure

Units of this type typically operate at pressures suitable for bioprocessing applications, generally up to a few MPa.

UV detection wavelengths

Commonly, variable UV detection is available, covering wavelengths relevant for protein and nucleic acid analysis.

System configurations

ÄKTA ready™ systems are typically available in isocratic, gradient, and extended configurations to suit various purification needs.

Power supply

Units commonly operate on standard industrial single-phase power, typically 230V, 50Hz for the UK market.

Footprint

For this model, the footprint is designed to be suitable for integration into bioprocessing suites, typically requiring moderate floor space.

Materials in contact with product

As a single-use system, product contact materials are typically medical-grade plastics, eliminating the need for cleaning validation.

• What is the primary benefit of a single-use chromatography system?

  The main benefit is the elimination of cleaning and cleaning validation between runs, which reduces downtime, minimises cross-contamination risk, and simplifies GMP compliance.

• Is this system suitable for GMP-regulated environments?

• Can this system handle different process volumes?

• What kind of maintenance does a single-use system require?

• What documentation is typically provided with such a system?

Chromatography systems command strong respect within analytical and pharmaceutical sectors. Buyers typically prioritise equipment with verified maintenance records and clear calibration history, as these directly affect analytical accuracy. Used units from established manufacturers remain highly valued for their reliability. Key strengths include reproducible results, robust construction, and established spare parts availability. Industry sentiment reflects confidence in these systems when sourced from reputable suppliers with transparent service documentation.

General overview for this equipment type