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尿素可提高冻干及干燥剂型保存过程中三价脊灰灭活疫苗的稳定性。

Urea Improves Stability of Inactivated Polio Vaccine Serotype 3 During Lyophilization and Storage in Dried Formulations.

机构信息

Department of Pharmaceutical Sciences, University of Colorado Anschutz Medical Campus, Aurora, Colorado 80045.

SanofiPasteur, March l'Etotile, France.

出版信息

J Pharm Sci. 2018 Aug;107(8):2070-2078. doi: 10.1016/j.xphs.2018.04.019. Epub 2018 Apr 27.

Abstract

Stable formulations of inactivated polio vaccine (IPV) could reduce cold-chain requirements and increase distribution of the vaccine to developing countries. Recently, significant improvement in thermal stability of IPV vaccines has been achieved by including urea in lyophilized formulations. In the present study, we investigated the effects of urea on recovery of potency of IPV after lyophilization and storage at 37°C and the correlation of potency recovery with key biophysical properties of IPV. By dynamic light scattering and transmission light microscopy, we found that loss of potency appeared to be due to agglomeration of virus particles during lyophilization and that moderate concentrations (e.g., 0.4 M) of urea reduced agglomeration and improved potency recovery. In addition, the relative thermal stability of the viron proteins was assessed after rehydration with temperature-dependent intrinsic fluorescence. Lyophilization of formulations without urea and postdrying storage resulted in reduced apparent melting temperatures in rehydrated samples. In formulations with urea, the rehydrated samples had thermal transitions and melting temperatures that were similar to those observed in aqueous control samples. Overall, the results indicated that in IPV formulations, urea improved potency recovery by inhibiting viron particle agglomeration and reducing denaturation of viron proteins.

摘要

稳定的灭活脊髓灰质炎疫苗(IPV)制剂可以降低冷链要求,并增加发展中国家对疫苗的分配。最近,通过在冻干制剂中加入尿素,IPV 疫苗的热稳定性得到了显著提高。在本研究中,我们研究了尿素对冻干和 37°C 储存后 IPV 效力恢复的影响,以及效力恢复与 IPV 的关键生物物理特性的相关性。通过动态光散射和透射光显微镜,我们发现效力损失似乎是由于病毒粒子在冻干过程中的聚集所致,而中等浓度(例如 0.4 M)的尿素可减少聚集并提高效力恢复。此外,还通过与温度相关的固有荧光评估了复水后病毒蛋白的相对热稳定性。无尿素制剂的冻干和干燥后储存导致复水样品的表观熔点降低。在含有尿素的制剂中,复水样品的热转变和熔点与在水性对照样品中观察到的相似。总体而言,结果表明在 IPV 制剂中,尿素通过抑制病毒粒子聚集和减少病毒蛋白变性来提高效力恢复。

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