Evaluation of heat inactivation of yellow fever vaccine residue in the filling bottle

R. Soares, B. Santos, Jouber Rocha, Izabella Santos, Y. Mendes
{"title":"Evaluation of heat inactivation of yellow fever vaccine residue in the filling bottle","authors":"R. Soares, B. Santos, Jouber Rocha, Izabella Santos, Y. Mendes","doi":"10.35259/isi.2022_52272","DOIUrl":null,"url":null,"abstract":"Objective: The aim of this study was to evaluate the heat inactivation of the Attenuated Yellow Fever vaccine residue contained in the bottle and accessories (hoses/needles of the filling system) using hot WFI water (90 o C) available at the DEPFI/Bio-Manguinhos/FIOCRUZ filling area. Methodology: After the filling process, approximately 20 or 45 liters of WFI water ≥80°C were added to the container with the vaccine residue. This volume of hot water was rinsed, including the filling system (hoses and pumps), and 50 ml samples were collected at the end of the line, at each established time: initial t0’, t05 ́, t10’, t15 ́, t20’ and t30’ and the temperature monitored during these time intervals. Three assays were performed to evaluate the inactivation by plaque assay using Vero cell culture. Results: The first viral inactivation assay was performed with approximately 20 L of hot water. The filling bottle temperature varied from 67.5 to 63.5 o C during the 20 minutes of the experiment. The results showed a reduction of the viral titer of 97.66% in the first 5 minutes and of 99.88% in 20 minutes. For the following tests, the volume of hot water added to the filling bottle was changed to 45 L, which increased the inactivation temperature in the filling bottle to the range of 66 to 71 o C. Under these conditions, it was possible to observe a 100% reduction in the viral titer after 30 minutes (2nd assay) and confirmation of these results is in progress (3rd assay). Conclusion: The initial results indicate the possibility that the proposed strategy of heat inactivation for the Attenuated Yellow Fever vaccine residue contained in the flask and accessories of the filling system using hot water could potentially applicable in the DEPFI/Bio-Manguinhos area and could be evaluated for other decontaminations in the unit. Further experiments will be needed to confirm these results.","PeriodicalId":8089,"journal":{"name":"Annals of the symposium: vaccines, biopharmaceuticals, in vitro diagnosis, management, other related themes","volume":"1 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Annals of the symposium: vaccines, biopharmaceuticals, in vitro diagnosis, management, other related themes","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.35259/isi.2022_52272","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Objective: The aim of this study was to evaluate the heat inactivation of the Attenuated Yellow Fever vaccine residue contained in the bottle and accessories (hoses/needles of the filling system) using hot WFI water (90 o C) available at the DEPFI/Bio-Manguinhos/FIOCRUZ filling area. Methodology: After the filling process, approximately 20 or 45 liters of WFI water ≥80°C were added to the container with the vaccine residue. This volume of hot water was rinsed, including the filling system (hoses and pumps), and 50 ml samples were collected at the end of the line, at each established time: initial t0’, t05 ́, t10’, t15 ́, t20’ and t30’ and the temperature monitored during these time intervals. Three assays were performed to evaluate the inactivation by plaque assay using Vero cell culture. Results: The first viral inactivation assay was performed with approximately 20 L of hot water. The filling bottle temperature varied from 67.5 to 63.5 o C during the 20 minutes of the experiment. The results showed a reduction of the viral titer of 97.66% in the first 5 minutes and of 99.88% in 20 minutes. For the following tests, the volume of hot water added to the filling bottle was changed to 45 L, which increased the inactivation temperature in the filling bottle to the range of 66 to 71 o C. Under these conditions, it was possible to observe a 100% reduction in the viral titer after 30 minutes (2nd assay) and confirmation of these results is in progress (3rd assay). Conclusion: The initial results indicate the possibility that the proposed strategy of heat inactivation for the Attenuated Yellow Fever vaccine residue contained in the flask and accessories of the filling system using hot water could potentially applicable in the DEPFI/Bio-Manguinhos area and could be evaluated for other decontaminations in the unit. Further experiments will be needed to confirm these results.
灌装瓶中黄热病疫苗残余物热灭活的评价
目的:本研究的目的是利用DEPFI/Bio-Manguinhos/FIOCRUZ灌装区提供的WFI热水(90℃),评估瓶中和附件(灌装系统的软管/针头)中含有的黄热病减毒疫苗残留物的热灭活效果。方法:灌装后,将≥80°C的WFI水约20或45升加入到含有疫苗残留物的容器中。将该体积的热水冲洗,包括灌装系统(软管和泵),并在每个确定的时间(初始时间为t0′,t05′,t10′,t15′,t20′和t30′)在管道末端收集50 ml样品,并在这些时间间隔内监测温度。采用Vero细胞培养的斑块法进行了三次失活试验。结果:第一次病毒灭活实验用约20 L热水进行。在20分钟的实验过程中,灌装瓶温度在67.5 ~ 63.5℃之间变化。结果表明,病毒滴度在前5分钟降低97.66%,20分钟降低99.88%。在接下来的测试中,将灌装瓶中加入的热水体积改为45 L,将灌装瓶中的失活温度提高到66 ~ 71℃。在这种条件下,可以观察到30分钟后病毒滴度降低100%(第二次检测),并且正在对这些结果进行确认(第三次检测)。结论:初步结果表明,采用热水对灌装系统的烧瓶和附件中含有的黄热病减毒疫苗残余物进行热灭活的策略可能适用于DEPFI/Bio-Manguinhos地区,并可用于该装置的其他净化。需要进一步的实验来证实这些结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信