Cell Banking
Master cell bank (MCB); Working cell bank (WCB)
The demand for nucleic acid-based gene therapies, novel vaccines, innovative therapeutic agents including messenger RNA (mRNA) and viral vectors is high. Plasmid DNA (pDNA) is the basis for all these advanced therapies. Wacker Biotech’s versatile plug-and-play platform PLASMITEC® is based on decades of hands-on experience in pDNA manufacturing for both early stage and Phase III clinical trials.
Wacker Biotech’s production site in San Diego serves as the location for cGMP manufacturing operations and is equipped with a 43 L single-use bioreactor and a 650 L stainless steel fermentation vessel, including scalable cell lysis. The company's more than 40 employees have extensive experience in the production of pDNA according to the quality guidelines of "Good Manufacturing Practice" (GMP) ranging from clinical startups to commercial product companies. pDNA can be used either directly for nucleic acid-based gene therapies and for vaccines or as a starting point for such innovative therapeutic agents, for example to manufacture messenger RNA (mRNA).
Wacker Biotech as a contract development and manufacturing organization (CDMO) supports its customers throughout the entire product lifecycle, right up to commercialization. Developed over decades, our plug-and-play platform for pDNA manufacturing offers great recovery and reliability, but also a highly flexible approach: we meet your needs and scale up, e.g. by adjusting fermentation and lysis conditions.
Master cell bank (MCB); Working cell bank (WCB)
Media development; Bacterial transformation; E. coli strains are provided by the customer or generated by WACKER; Manufacturing in 43 L single-use and 650 L stainless steel fermenters in GMP quality
Harvest by continuous-flow centrifugation; Cell disruption using alkaline lysis; Its advantage is the scability to meet the needs of each project
2-column purification scheme along with depth filtration and tangential flow filtration (TFF)
Final 0.2 μm filtration for the bulk drug substance after the final TFF concentration. We can fill into a client’s desired container (i.e. PETG bottles or ULDPE cryogenic storage bags); Storage at -70 °C
In the first step of pDNA production, an initial plasmid construct is used to generate production cell banks. This is followed by fermentation in larger reactors, where the actual production of the plasmid DNA takes place. Subsequently, the cell paste produced during fermentation is harvested and the plasmid is extracted from the cell paste by a process of alkaline scalable lysis. In a multi-step purification process, the extracted pDNA molecules are then separated from undesirable components, purified and concentrated. In the final step the finished pDNA can be filled into a client’s desired container.
Accumulated experience of more than 18 years in manufacturing plasmids as DS and DP for all stages of clinical studies, including but not limited to Phase III
More about therapeutic proteins, vaccines, plasmid DNA and live microbial products
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