ÄKTA process
Industrial liquid chromatography system

ÄKTA process equipment is designed for companies transitioning from laboratory development to commercial production of biological pharmaceuticals. The system is used in the production of monoclonal antibodies, recombinant proteins, conjugate vaccines, and plasmid DNA at the clinical trial and industrial production stages. The line includes three models, covering virtually any production scale. The entry-level model delivers flow rates of 1–180 liters per hour, the mid-range model delivers 3–600 liters per hour, and the flagship model delivers 10–2000 liters per hour. Customers select the version based on the column diameter and the required line throughput. Depending…

Country of origin: USA
Please check with our managers for detailed purchase conditions
ÄKTA process
An industrial chromatography system for large-scale purification of biopharmaceuticals. It covers flow rates from 1 to 2,000 liters per hour and fully complies with GMP requirements.

ÄKTA process equipment is designed for companies transitioning from laboratory development to commercial production of biological pharmaceuticals. The system is used in the production of monoclonal antibodies, recombinant proteins, conjugate vaccines, and plasmid DNA at the clinical trial and industrial production stages. The line includes three models, covering virtually any production scale. The entry-level model delivers flow rates of 1–180 liters per hour, the mid-range model delivers 3–600 liters per hour, and the flagship model delivers 10–2000 liters per hour. Customers select the version based on the column diameter and the required line throughput. Depending…

Country of origin: USA
Please check with our managers for detailed purchase conditions
ÄKTA process
An industrial chromatography system for large-scale purification of biopharmaceuticals. It covers flow rates from 1 to 2,000 liters per hour and fully complies with GMP requirements.
ÄKTA process industrial liquid chromatography system
ÄKTA process equipment is designed for companies transitioning from laboratory development to commercial production of biological pharmaceuticals. The system is used in the production of monoclonal antibodies, recombinant proteins, conjugate vaccines, and plasmid DNA at the clinical trial and industrial production stages. The line includes three models, covering virtually any production scale. The entry-level model delivers flow rates of 1–180 liters per hour, the mid-range model delivers 3–600 liters per hour, and the flagship model delivers 10–2000 liters per hour. Customers select the version based on the column diameter and the required line throughput. Depending on the aggressiveness of the media and operating temperatures, two types of materials are used. Stainless steel with an electropolished inner surface withstands pressures up to 10 bar and is compatible with organic solvents. Polypropylene is rated for 6 bar and is used for aqueous buffers at room temperature—this solution reduces the cost of the system in applications where chemical resistance of the metal is not required. The system is assembled modularly from standardized components. The component library contains over a million possible configurations, allowing the system to be customized for a specific process flow: add additional inputs, install parameter monitoring sensors, and enable online buffer dilution from concentrated solutions. The Intelligent Packing algorithm automates the packing of industrial columns up to 1600 mm in diameter, ensuring batch-to-batch reproducibility. Control is available in two versions. The standalone version is controlled by UNICORN software, which supports complex gradient profiles, automatic peak detection, and full documentation in accordance with 21 CFR Part 11. The centralized control version integrates into the plant network via OPC-UA or EtherNet/IP protocols, allowing for monitoring of the chromatography process from a single control room. The manufacturer has provided for all aspects of GMP operation. Materials in contact with the product are USP Class VI certified and do not contain animal-derived components. Integrated cleaning-in-place (CIP) and sterilization-in-place (SIP) procedures eliminate cross-contamination between batches. A dual filter with differential pressure control ensures the absence of particulate matter in the final product.
