Purification of Monoclonal Antibodies with BioPro SmartSep

Purification

Purification of Monoclonal Antibodies with BioPro SmartSep

08 Mar, 2017

Published over 9 years ago. See the latest and most current information on Purification.

Michael Ostendorf
2 min read
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Challenges During mAb Purification

For purification of monoclonal antibodies, high demands are required from the separating material. Factors influencing the binding characteristics of IgG are pH, linear velocity and/or salt concentration (conductivity) at the time the sample is loaded onto the column. 

Therefore, a material with highly stable performance is required with regard to all those factors. In order to demonstrate the performance of YMC-BioPro materials, several studies have been performed. 

• Purification of Adalimumab

• Influence of pH

• Influence of linear velocity

• Influence salt concentration

In order to demonstrate the behaviour of BioPro SmartSep under different elution condi¬tions, experiments with different values of pH, linear velocity and salt concentration were performed and the dynamic binding capacity (DBC) recorded.

The parameters changed were: 

Experimental Conditions

pH: 6.0 vs. 5.3  

Linear velocity: 200 - 800 cm/hr  

Salt concentration: 0 - 50 mM NaCl  

BioPro SmartSep S30 particles 

Influence of pH 

High binding capacities are achieved regardless of elution of pH. Therefore, milder eluting conditions for Adalimumab can be selected.

Influence of Linear Velocity

BioPro SmartSep maintains higher binding capacity values over a wider range of linear velocity. This will increase product throughput for the purification work without loss of efficiency.

Influence of Salt Concentration

BioPro SmartSep has higher salt concentration tolerance. This simplifies the desalting pro¬cess after Protein A chromatography and will help to shorten the production process.

Conclusions 

BioPro SmartSep materials meet the highest demands for the purification of monoclonal antibodies. High binding capacity is achieved regardless of elution of pH, linear velocity or salt concentration. This allows purification processes to be carried out more efficiently. 

• Milder eluting conditions can be selected 

• Higher throughput at stable efficiencies 

• Simplification of desalting processes for shorter processes 

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