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Efficient extraction of adventitious virus nucleic acid using commercially available methods.
Valiant, William G; Borman, Jon; Cai, Kang; Vallone, Peter M.
Affiliation
  • Valiant WG; Biomolecular Measurement Division, Applied Genetics Group, National Institute of Standards and Technology, Gaithersburg, MD, USA.
  • Borman J; Biopharmaceutical Development, Biopharmaceuticals R&D, AstraZeneca, Gaithersburg, MD, USA.
  • Cai K; Biopharmaceutical Development, Biopharmaceuticals R&D, AstraZeneca, Gaithersburg, MD, USA.
  • Vallone PM; Biomolecular Measurement Division, Applied Genetics Group, National Institute of Standards and Technology, Gaithersburg, MD, USA. Electronic address: peter.vallone@nist.gov.
Biologicals ; 85: 101741, 2024 Feb.
Article in En | MEDLINE | ID: mdl-38157678
ABSTRACT
An essential step in pharmaceutical product development is screening for contamination with adventitious agents, and there is desire to develop highly sensitive assays to detect adventitious viral nucleic acid. This study sought to examine the nucleic acid extraction efficiency of three viral candidates in relevant background matrices using four different extraction methods. Three model adventitious viruses, Minute virus of Mice, Porcine Circovirus, and Feline Leukemia Virus, were diluted within a variety of background matrices relevant to pharmaceutical production methods. Upon extraction, the nucleic acid was quantified using droplet digital PCR methods. Four nucleic acid extraction methods were assessed, including commercially available kits and manual extraction methods. Each method recovered nucleic acid post-extraction for each of the model viruses within the tested background matrices. The silica-column based method recovered a greater amount of viral nucleic acid, compared to the other methods tested. Similar trends were observed when model virus was diluted in bioreactor supernatant, which replicates industry testing conditions and provides details on which extraction methods might be used in Next Generation Sequencing and PCR methods for detecting contamination within pharmaceutical products.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Viruses / DNA, Viral Limits: Animals Language: En Journal: Biologicals Journal subject: ALERGIA E IMUNOLOGIA Year: 2024 Document type: Article Affiliation country: Estados Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Viruses / DNA, Viral Limits: Animals Language: En Journal: Biologicals Journal subject: ALERGIA E IMUNOLOGIA Year: 2024 Document type: Article Affiliation country: Estados Unidos