...
首页> 外文期刊>Vaccine >Novel formulations enhance the thermal stability of live-attenuated flavivirus vaccines.
【24h】

Novel formulations enhance the thermal stability of live-attenuated flavivirus vaccines.

机译:新型制剂增强了减毒活黄病毒疫苗的热稳定性。

获取原文
获取原文并翻译 | 示例
           

摘要

Thermal stability is important for the manufacture, distribution and administration of vaccines, especially in tropical developing countries, where particularly adverse field conditions exist. Current live-attenuated flavivirus vaccines exhibit relatively poor liquid stability in clinical settings, and clinicians are instructed to discard the yellow fever vaccine 1 h after reconstitution. We have identified novel combinations of excipients that greatly enhance the thermal stability of live-attenuated DEN-2 PDK-53-based flavivirus vaccine candidates. Liquid formulations comprising a sugar, albumin and a pluronic polymer minimized the loss of flavivirus infectious titer to less than 0.5 log10 pfu after storage for at least 8 h at 37 degrees C, 7 days at room temperature or at least 11 weeks at 4 degrees C. Additionally, these formulations prevented reduction of viral infectivity after two freeze-thaw cycles of virus. Formulated candidate vaccines were readily lyophilized and reconstituted with minimal loss of viral titers. In mice, the formulations were safe and did not hinder the ability of the vaccine virus to generate a potent, protective immune response. These formulations provided significantly greater liquid-phase stability than has been reported previously for other flavivirus vaccine formulations. The enhanced thermal stability provided by the formulations described here will facilitate the effective distribution of flavivirus vaccines worldwide.Digital Object Identifier http://dx.doi.org/10.1016/j.vaccine.2011.07.054
机译:热稳定性对于疫苗的生产,分发和管理非常重要,特别是在热带发展中国家,那里存在特别不利的野外条件。当前的减毒活黄病毒疫苗在临床环境中表现出相对较差的液体稳定性,并指示临床医生在重构后1小时内丢弃黄热病疫苗。我们已经确定了赋形剂的新型组合,它们可以大大增强减毒的基于DEN-2 PDK-53的黄病毒活候选疫苗的热稳定性。包含糖,白蛋白和普朗尼克聚合物的液体制剂在37摄氏度,室温或室温下保存7天或以上至少8小时后,将黄病毒感染滴度的损失降至最低,低于0.5 log 10 pfu。在4摄氏度下至少11周。此外,这些制剂防止了病毒的两个冻融循环后病毒感染力的降低。配制的候选疫苗易于冻干并重组,且病毒滴度损失最小。在小鼠中,该制剂是安全的,并且不妨碍疫苗病毒产生有效的保护性免疫应答的能力。与以前针对其他黄病毒疫苗制剂的报道相比,这些制剂提供的液相稳定性明显更高。本文所述配方提供的增强的热稳定性将促进黄病毒疫苗在全球的有效分布。数字对象标识符http://dx.doi.org/10.1016/j.vaccine.2011.07.054

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号