Application of multivirus spike approach for viral clearance evaluation

Viral contamination is a common risk to continuous cell line‐derived biologics. Viral validation is thus required for license applications. Viral validation for chromatography procedures is routinely performed by spiking a model virus into the load material and performing the chromatography procedur...

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Bibliographic Details
Published inBiotechnology and bioengineering Vol. 84; no. 6; pp. 714 - 722
Main Authors Valera, Christine R., Chen, Janice W., Xu, Yuan
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc., A Wiley Company 20.12.2003
Wiley
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Summary:Viral contamination is a common risk to continuous cell line‐derived biologics. Viral validation is thus required for license applications. Viral validation for chromatography procedures is routinely performed by spiking a model virus into the load material and performing the chromatography procedures at small scale under conditions equivalent to the commercial scale. With traditional cell‐based infectivity assays, one can only spike one model virus at one time. Quantitative PCR methods (TaqMan) make it possible to spike multiple model viruses for a chromatography procedure simultaneously. TaqMan assays can quantify multiple types of viruses and other types of nucleic acid in a single sample without cross interference because of its extremely high specificity. Therefore, a multivirus spike approach was evaluated and compared to a single virus spike approach. The study was further extended to the evaluation of host cell DNA clearance. The data shows highly comparable viral and host cell DNA clearance between the single and multiple virus spike approaches. Application of a multivirus spike approach provides significant time, manpower, and cost savings for new drug development. © 2003 Wiley Periodicals, Inc. Biotechnol Bioeng 84: 714–722, 2003.
Bibliography:istex:8D683F8220EC1E941BD2EDF307F694CC188D2C52
ark:/67375/WNG-TH041FCB-Z
ArticleID:BIT10825
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0006-3592
1097-0290
DOI:10.1002/bit.10825