Remove Resources Separation-Purification
article thumbnail

Rapid method development to overcome challenges of bi-specific antibody purification

European Pharmaceutical Review

Downstream purification approaches. Due to their structural similarities, many current bsAb downstream purification methodologies are based on established mAb purification processes, using platform affinity, charge, hydrophobicity and mixed mode-based purification. Figure 1: Example of bi-specific formats.

article thumbnail

Novel nanofiltration method for microbial biosurfactant downstream processing

European Pharmaceutical Review

A study has reported for the first time, an innovative downstream method for mannosylerythritol lipids (MELs), were separated from the crude MEL mixture in a first stage with the other lipid derivatives (free fatty acids, mono- and diacylglycerols) removed by organic solvent nanofiltration (OSN).

69
Insiders

Sign Up for our Newsletter

This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.

Trending Sources

article thumbnail

Collaboration to support quality production of biologics

European Pharmaceutical Review

#atccnews [link] pic.twitter.com/LF38xxYvWM — ATCC (@officialatcc) February 23, 2023 The solutions the organisations will launch together include: Genomic DNA from top cell lines used in bioproduction Measurement of cellular DNA left over following purification is required by regulatory authorities to ensure product safety.

77
article thumbnail

Optimising bispecific antibody clonal cell selection with high-throughput analytics

European Pharmaceutical Review

A delicate balance between the high-resource obligations of extensive testing and the importance of the choice means manufacturers are motivated to employ improved strategies for clone screening and characterisation at the earliest stages. Fortunately, high-throughput automated liquid handling purification platforms can be utilised.

article thumbnail

Considerations for a Decentralized Manufacturing Paradigm

ISPE

12 , 28 , 29 , 30 , 31 Advantages SUT creates closed systems, which separates operators and rooms, enables aseptic transfer between containers, and mitigates the risk of cross-contamination. It also reduces environmental impact because it requires fewer chemicals and less high-purity water and heat.

article thumbnail

Challenges for Net Zero Carbon Pharmaceutical Manufacturing

ISPE

Using fewer resources to deliver the same or more output is inherent in pharmaceutical business practices. With rising global demand for energy, doing more with fewer resources is good for the planet, business, and consumers. 5 a b World Resources Institute and World Business Council for Sustainable Development.

article thumbnail

ISPE Launches Enabling Global Pharma Innovation: Delivering for Patients

ISPE

ICH has the mission “to achieve greater harmonization worldwide to ensure that safe, effective, and high-quality medicines are developed and registered in the most resource-efficient manner.” Harmonization of global regulatory requirements has been progressing for more than thirty years under the International Council for Harmonisation (ICH).

Dosage 95