European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V · 2026
Systematic evaluation of cryopreservation parameters for natural killer cells in clinically relevant cyclic olefin polymer vials.
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Juliano Michael, Garcia Braden, Nguyen Henry, Potnis Manali, Cornell Linara, Khan Krishnendu
Аннотация
BACKGROUND AIMS: Allogeneic cell therapy uses donor-derived cells to treat disease indications in oncology, autoimmune disorders, and other areas. Unlike patient-specific autologous therapies, allogeneic therapies are manufactured in large batches. For these products, the final containment is critical for maintaining cell viability and function. Factors such as material composition, container closure integrity at cryogenic temperatures, and container-cell interactions directly affect post-thaw recovery and performance. This study evaluates key cryogenic storage parameters for NK-92 cells used in allogeneic therapies in a clinically relevant cyclic olefin polymer (COP) vial.
METHODS: In this study, parameters such as freezing rate, cell density, and the presence of DMSO as a cryoprotective agent during the freezing process in COP vials were evaluated. Additionally, the effect of ice nucleation was measured, and a direct comparison of freezing these cells in COP vials versus cryobags was investigated. The effect on cells post-thawing was determined by measuring its recovery, viability, proliferation, cytokine secretion, and tumor killing ability.
RESULTS: Freezing rates of -1 and -5°C/min were found to be optimal for NK-92 cell storage in COP vials. DMSO as the cryoprotectant improved post-thaw proliferation, lower cell density during freezing enhanced recovery, and in contrast, higher cell density increased cytokine secretion. Ice nucleation timing on the other hand had no significant impact on NK-92 cell viability or function. Compared head-to-head, cells frozen in COP vials demonstrated superior post-thaw tumor killing activity versus cells stored in bags.
CONCLUSION: This study to our knowledge provides the first comprehensive analysis of cryopreservation conditions for therapeutically relevant allogeneic cell therapy products in a clinically relevant vial, which is crucial to ensure their effectiveness upon reaching patients.
METHODS: In this study, parameters such as freezing rate, cell density, and the presence of DMSO as a cryoprotective agent during the freezing process in COP vials were evaluated. Additionally, the effect of ice nucleation was measured, and a direct comparison of freezing these cells in COP vials versus cryobags was investigated. The effect on cells post-thawing was determined by measuring its recovery, viability, proliferation, cytokine secretion, and tumor killing ability.
RESULTS: Freezing rates of -1 and -5°C/min were found to be optimal for NK-92 cell storage in COP vials. DMSO as the cryoprotectant improved post-thaw proliferation, lower cell density during freezing enhanced recovery, and in contrast, higher cell density increased cytokine secretion. Ice nucleation timing on the other hand had no significant impact on NK-92 cell viability or function. Compared head-to-head, cells frozen in COP vials demonstrated superior post-thaw tumor killing activity versus cells stored in bags.
CONCLUSION: This study to our knowledge provides the first comprehensive analysis of cryopreservation conditions for therapeutically relevant allogeneic cell therapy products in a clinically relevant vial, which is crucial to ensure their effectiveness upon reaching patients.