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Quality and Consistency of Cell Culture M edia with a Highlight on FMDV

Quality and Consistency of Cell Culture M edia with a Highlight on FMDV. Dr. Serge Ohresser 4th International Conference on Vaccines & Vaccination, September 24, 2014 - Valencia. Bioproduction Process. Upstream Processing

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Quality and Consistency of Cell Culture M edia with a Highlight on FMDV

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  1. Quality and Consistency of Cell Culture Media with a Highlight on FMDV Dr. Serge Ohresser 4th International Conference on Vaccines & Vaccination, September 24, 2014 - Valencia

  2. Bioproduction Process • Upstream Processing • Most of the critical quality attributes of a final product in biological process are determined in Upstream steps • Minor changes in cell culturemedia or bioreactor conditions can effect the end product • Process Improvements • Moving to simplified and more defined composition of media • Consistency of cell culture media minimizes risks of deviation in biological processes • Raw material qualification and chemical expertise in media production Valencia Vaccine congress

  3. Risks in Upstream Processing • “Raw Materials as a Source of Contamination in Large-Scale Cell Culture” • Particular risk for virus & bacterial contamination • Arising awareness for upstream virus safety from high profile contaminations • Manufacturing process bears multiple sources of potential adventitious virus(e.g. facility, equipment, process, materials, utilities, personnel) • Raw materials are important pillars of cell culture media formulations: • Origin – important for risk assessment • Traceability – qualification and documentation • Qualification – suitability for cell culture media and consistency Valencia Vaccine congress

  4. Selection of high traceable materials • In-coming testing • Serum bovine guideline • Virus clearance at manufacturer • Serum-free media • Recombinant protein alternatives • Chemically defined media • Non-animal origin Selection of Raw Materials Reduce concerns of animal origin contaminants Traceability and testing Maximize control of animal derived products Moving towards alternatives to animal origin products Moving towards chemically defined Valencia Vaccine congress

  5. Cell Culture Media Quality and Performance… What Makes the Difference? Valencia Vaccine congress

  6. Cell Culture Media Quality Matters • Product Homogeneity • Consistent process by constant particle size distribution over all scales • Gentle Milling • Oxygen or temperature sensitive raw materials handled with care by gently milling technology • Media Formulation • Enhanced component solubility and concentration to optimal formulation design Homogenous Merck Millipore medium vs. competitors medium showing crystals and in-homogenous blending White appearance of suppliers media, while Merck Millipore medium preserves the pinkish color resulting form vitamin B Pre-treated raw materials can enhance their solubility Valencia Vaccine congress

  7. Merck Millipore Cell Culture Media Products • Consistent performing cell culture media • Formulation improvement by physico-chemical expertise • Comprehensive raw material qualification process • Gentle manufacturing process • Comprehensive documentation and regulatory support • Cell Culture media products • Customized DPM – according to customer formulations • Cellvento™ CHO – optimized for CHO cell cultures • Cellvento™ BHK – optimized for BHK-21 cell cultures Valencia Vaccine congress

  8. A Highlight on FMDV Production Improvement Foot-and-mouth disease (FMD), an infectious and sometimes fatal viral disease that affects cloven-hoofed animals • The production process • Complex media used for cultivation of BHK-21 cells for FMDV production, e.g. GMEM + TPB + 10% adult bovine serum • Similar GMP requirements as media for human vaccine manufacturing • Highly potent vaccine needs to be produced at low cost • Serum-free compositions become a must • Due to high variability of serum • Risk of introducing adventitious agent into the process • Serum may contain antibodies against FMDV • Associated cost of supply & serum treatment before process entering Valencia Vaccine congress

  9. Comparison of Serum-containing and Serum-free Process Serum-Containing Process Virus inoculation and propagation 48h Cell Culture 48h Sedimentation 18h Media change and Cell Recovery 12h serum transfer to new tank transfer to new tank media + serum 8-10% PEG Serum-free Process Cell Culture 48 - 60h Virus inoculation and propagation Add 30% as ‚feed‘ serum-free media Start with 70% working volume transfer to new tank

  10. Serum-free Process for FMDV Production Advantages • No extra serum needed • No need for serum batch testing • No additional depletion of anti-FMDV Abs • No exchange of media before viral growth • Non-animal origin raw materials • More defined composition • Simple upstream process Less process costs Simplified process Safety/less regulatory exposure Process consistency Easier downstream purification Valencia Vaccine congress

  11. Cellvento™ BHK-200 is an Optimal Serum-free Medium for a Batch Culture Vaccine Process Rapid growth of BHK21 cells Infection performed early in the culture High viral amplification High antigen content Cellvento™ BHK-200 medium along the overall vaccine process chain: • Establishment of master and working cell bank • Adaptation from serum-containing to serum-free conditions • Scale-up from lab to production scale • High-density cell propagation • Amplification of FMD virus for industrial production Valencia Vaccine congress

  12. BHK-21 Cell Growth in Cellvento™ BHK-200 Medium Growth of BHK-21 cells in a batch culture experiment • Metabolic profile was analyzed during growth • Glucose consumed at day 5 with maximum cell density of 6.5x106 cells/mL Valencia Vaccine congress

  13. Classical Media vs. Cellvento™ BHK-200 Medium Comparison Cellvento™ BHK-200 medium vs. GMEM + TPB + 10% serum Double maximum Viable Cell Density with Cellvento™ BHK-200 medium. With GMEM, growth stops after day 3 while Glucose is not a limiting factor.

  14. Performance of Cellvento™ BHK-200 Medium Infection of BHK21 cells with 3 FMDV strains at a concentration of 1.5 x106cells/ml in 250 ml shaker flasks (37 °C, pH 7.4) Antigen content (146S) FMDV Sensitivity Test – TCID50 Antigen produced was evaluated using TCID50 and 146S measurement methods: Comparable antigen mass produced similar to classical serum-containing conditions. Valencia Vaccine congress

  15. Concluding Remarks • Serum-containing processes are complex, costly, difficult to standardize, regulatory non-friendly and bear the risk of adventitious agents in the upstream process • Cell culture media performance is directly linked to the media formulation, quality of raw materials and the manufacturing process • Avoidance of serum requires media optimization and translation into a manufacturable recipe • Serum-free media can be used to grow BHK21 cells and subsequently infect them to produce the FMD antigen • Cellvento™ BHK-200 medium is a suitable formulation for serum-free FMDV manufacturing processes Valencia Vaccine congress

  16. Thankyou!Dr. Serge OhresserUpstream Sales Development, InternationalPharm Chemicals SolutionsMerck MilliporeEmail: serge.ohresser@merckgroup.com Valencia Vaccine congress

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