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Case Study on Quantitation and Characterization of

Polysorbate-80 in Drug Formulations

Polysorbate-80 (PS-80) is a surfactant commonly used as an excipient to improve API stability. However, degradation of PS-80 can lead to decreased drug potency or stability, and there is inconsistency in the quality and composition of PS-80 provided by different vendors.


Download this case study to learn the following:

  • Challenges associated with the heterogeneous nature of PS-80 when used as an excipient
  • Strategies to quantitate and characterize PS-80
  • How this combined approach can measure PS-80 stability and homogeneity

Q&A on Strategies to Remove Formulation Development from the Critical Path

Biopharmaceuticals are highly unstable, and formulation development is required to ensure drug product quality and stability during manufacturing, storage and clinical administration. Further, formulation development is often on the critical path at risk of delaying IND and BLA fillings.

 

Download this Q&A with Dr. Jun Lu, Director, Analytical Development to learn the following:

  • How automation can be leveraged to remove formulation development from the critical path
  • Strategies to overcome challenges associated with ranking protein stability
  • Where instruments such as the Uncle platform can be used during the process

Learn About Development & Drug Substance

Biomanufacturing Services at Catalent

Catalent Biologics’ development services span drug substance, drug product and analytical leveraging advanced technology and proven expertise.

 

Download Now

Catalent Biologics’ two state-of-the-art biomanufacturing facilities have been designed to provide integrated bulk drug substance services for clinical trials and commercial supply.

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