Your browser doesn't support javascript.
loading
Lentivirus capture directly from cell culture with Q-functionalised microcapillary film chromatography.
Darton, N J; Darling, D; Townsend, M J; McNally, D J; Farzaneh, F; Slater, N K H.
Affiliation
  • Darton NJ; Department of Chemical Engineering and Biotechnology, New Museums Site, Pembroke St, Cambridge CB2 3RA, UK. Electronic address: nickdarton@cantab.net.
  • Darling D; King's College London, 123 Coldharbour Lane, London SE5 9NU, UK.
  • Townsend MJ; Department of Chemical Engineering and Biotechnology, New Museums Site, Pembroke St, Cambridge CB2 3RA, UK.
  • McNally DJ; Department of Chemical Engineering and Biotechnology, New Museums Site, Pembroke St, Cambridge CB2 3RA, UK.
  • Farzaneh F; King's College London, 123 Coldharbour Lane, London SE5 9NU, UK.
  • Slater NKH; Department of Chemical Engineering and Biotechnology, New Museums Site, Pembroke St, Cambridge CB2 3RA, UK.
J Chromatogr A ; 1251: 236-239, 2012 Aug 17.
Article in En | MEDLINE | ID: mdl-22771068
ABSTRACT
A new disposable adsorbent material for fast anion-exchange capture of nano-complexes without prefiltering, clarification or pre-processing of samples was developed based on plastic microcapillary films (MCFs). An MCF containing 19 parallel microcapillaries, each with a mean internal diameter of 142 ± 10 µm, was prepared using a melt extrusion process from an ethylene-vinyl alcohol copolymer (EVOH). The MCF internal surfaces were functionalised using branched chain chemistries to attach quaternary amine groups producing an anion-exchange adsorbent. The purification of nano-complexes using this newly fabricated MCF-EVOH-Q was successfully demonstrated with the capture of lentivirus from pre-filtered culture harvest. This 5m chromatographic substrate was found to bind and elute ∼40% of bound lentivirus or 2.5 × 10(6)infectious units (ifu). The unique properties of this chromatographic substrate that allow the passage of large particulates was further demonstrated with the capture of lentiviral particles from unfiltered un-processed culture media containing cells and cell debris. Using this approach, 56% or 1 × 10(7)ifu of captured lentivirus was eluted. A device based on this new material might be used at an early stage in clinical lentiviral production to harvest lentiviral particles, directly from bioreactors.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chromatography, Ion Exchange / Lentivirus / Cell Culture Techniques / Genetic Vectors Limits: Humans Language: En Journal: J Chromatogr A Year: 2012 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chromatography, Ion Exchange / Lentivirus / Cell Culture Techniques / Genetic Vectors Limits: Humans Language: En Journal: J Chromatogr A Year: 2012 Document type: Article