Adherent Cell Culture

Overview

Adherent cell culture platforms provide scalable options with increasing cell growth surface areas for production, and the option to utilize available scale-up technologies is essential not only to meet the required cell demand, but also to limit the costs of manufacturing.

Esco Aster offers services to develop cell expansion and scale-up manufacturing strategies of adherent cell culture, whether primary cells or cell lines, , regardless of the development status. Our cell culture process development services support clients' specific requirements for cell culture process development including process parameter optimisation and can incorporate release criteria and quality attribute testing.

OUR SERVICES

Our services encompass the following areas:

Upstream Process Development and Optimisation

hMSC Release Criteria and Quality Attributes

Upstream Process Development and Optimisation

Esco Aster offers clients the service to develop cell expansion and scale-up manufacture of human mesenchymal stromal cells (MSCs) isolated from various sources, regardless of development status.

Parameters such as hMSC seeding density, growth duration, harvesting parameters, and media exchange intervals would be optimised with emphasis on goals to reduce costs, increase efficiency, and maximise yield whilst not compromising hMSC quality.

Metabolite and media analysis, including but not limited to glucose, pH change, cellular waste products, as well as cell morphology monitoring via fluorescence imaging are utilised to ascertain the ideal process conditions and parameters.

Process Development and Optimisation

Release Criteria and Quality Attributes

Expanded cells can be screened for various quality release criteria respective to the cells, such as the ‘Minimal criteria for defining multipotent mesenchymal stromal cells (MSCs)’ established by the International Society of Cellular and Gene Therapy (ISCT) for expanded MSCs, or pluripotent markers, and ability to differentiate into 3 germ layers (ecto-, endo- and mesoderm) such as in the case for induced pluripotent stem cells.

In addition, the option for usage of xeno-free or GMP certified cell culture media and reagents paves the pathway towards clinical manufacturing and regulatory approval of expanded cells. 

hMSC Release Criteria and Quality Attributes