Institute of Veterinary Immunology & Engineering, National Research Center of Engineering and Technology for Veterinary Biologicals, Jiangsu Academy of Agricultural Sciences, Nanjing, 210014, China.
Department of Biochemistry, School of Life Sciences, College of Agriculture, Engineering & Science, University of KwaZulu-Natal, Pietermaritzburg, 3209, South Africa.
Appl Microbiol Biotechnol. 2024 Jun 5;108(1):359. doi: 10.1007/s00253-024-13174-7.
Vacuum foam drying (VFD) has been shown to improve the thermostability and long-term shelf life of Newcastle Disease Virus (NDV). This study optimized the VFD process to improve the shelf life of NDV at laboratory-scale and then tested the optimized conditions at pilot-scale. The optimal NDV to T5 formulation ratio was determined to be 1:1 or 3:2. Using the 1:1 virus to formulation ratio, the optimal filling volumes were determined to be 13-17% of the vial capacity. The optimized VFD process conditions were determined to be at a shelf temperature of 25℃ with a minimum overall drying time of 44 h. The vaccine samples prepared using these optimized conditions at laboratory-scale exhibited virus titer losses of ≤ 1.0 log with residual moisture content (RMC) below 3%. Furthermore, these samples were transported for 97 days around China at ambient temperature without significant titer loss, thus demonstrating the thermostability of the NDV-VFD vaccine. Pilot-scale testing of the NDV-VFD vaccine at optimized conditions showed promising results for up-scaling the process as the RMC was below 3%. However, the virus titer loss was slightly above 1.0 log (approximately 1.1 log). Therefore, the NDV-VFD process requires further optimization at pilot scale to obtain a titer loss of ≤ 1.0 log. Results from this study provide important guidance for possible industrialization of NDV-VFD vaccine in the future. KEY POINTS: • The process optimization and scale-up test of thermostable NDV vaccine prepared through VFD is reported for the first time in this study. • The live attenuated NDV-VFD vaccine maintained thermostability for 97 days during long distance transportation in summer without cold chain conditions. • The optimized NDV-VFD vaccine preparations evaluated at pilot-scale maintained acceptable levels of infectivity after preservation at 37℃ for 90 days, which demonstrated the feasibility of the vaccine for industrialization.
真空泡沫干燥(VFD)已被证明可以提高新城疫病毒(NDV)的热稳定性和长期货架寿命。本研究在实验室规模上优化了 VFD 工艺,以提高 NDV 的货架寿命,然后在中试规模上测试了优化条件。确定 NDV 与 T5 制剂的最佳配方比例为 1:1 或 3:2。使用 1:1 的病毒与制剂比例,确定最佳填充体积为瓶容量的 13-17%。优化的 VFD 工艺条件确定为 25℃的搁板温度,总干燥时间至少为 44 小时。在实验室规模下使用这些优化条件制备的疫苗样品显示病毒滴度损失≤1.0 log,残留水分含量(RMC)低于 3%。此外,这些样品在中国各地在环境温度下运输了 97 天,没有明显的滴度损失,从而证明了 NDV-VFD 疫苗的热稳定性。在优化条件下对 NDV-VFD 疫苗进行中试测试表明,该过程具有扩大规模的潜力,因为 RMC 低于 3%。然而,病毒滴度损失略高于 1.0 log(约 1.1 log)。因此,NDV-VFD 工艺需要在中试规模上进一步优化,以获得≤1.0 log 的滴度损失。本研究的结果为未来 NDV-VFD 疫苗的工业化提供了重要指导。 要点: • 首次报道了通过 VFD 制备耐热 NDV 疫苗的工艺优化和放大试验。 • 在夏季没有冷链条件的情况下,长途运输期间,活减毒 NDV-VFD 疫苗保持了热稳定性,97 天。 • 在中试规模下评估的优化 NDV-VFD 疫苗制剂在 37℃保存 90 天后保持了可接受的感染性水平,这证明了该疫苗工业化的可行性。