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Nanofiltration as a robust method contributing to viral safety of plasma-derived therapeutics: 20 years' experience of the plasma protein manufacturers.
Roth, Nathan J; Dichtelmüller, Herbert O; Fabbrizzi, Fabrizio; Flechsig, Eckhard; Gröner, Albrecht; Gustafson, Mary; Jorquera, Juan I; Kreil, Thomas R; Misztela, Dominika; Moretti, Elisa; Moscardini, Mila; Poelsler, Gerhard; More, John; Roberts, Peter; Wieser, Andreas; Gajardo, Rodrigo.
Afiliação
  • Roth NJ; CSL Behring, Bern, Switzerland.
  • Dichtelmüller HO; Biotest, Dreieich, Germany.
  • Fabbrizzi F; Kedrion, Castelvecchio Pascoli, Italy.
  • Flechsig E; Biotest, Dreieich, Germany.
  • Gröner A; CSL Behring, Marburg, Germany.
  • Gustafson M; PPTA, Annapolis, Maryland, USA.
  • Jorquera JI; Grifols, Sant Cugat del Vallès, Spain.
  • Kreil TR; Takeda, Vienna, Austria.
  • Misztela D; PPTA, Brussels, Belgium.
  • Moretti E; Kedrion, Castelvecchio Pascoli, Italy.
  • Moscardini M; Kedrion, Castelvecchio Pascoli, Italy.
  • Poelsler G; Biotest, Dreieich, Germany.
  • More J; BioProducts Laboratory, Elstree, UK.
  • Roberts P; BioProducts Laboratory, Elstree, UK.
  • Wieser A; Takeda, Vienna, Austria.
  • Gajardo R; Grifols, Sant Cugat del Vallès, Spain.
Transfusion ; 60(11): 2661-2674, 2020 11.
Article em En | MEDLINE | ID: mdl-32815181
ABSTRACT

BACKGROUND:

Nanofiltration entails the filtering of protein solutions through membranes with pores of nanometric sizes that have the capability to effectively retain a wide range of viruses. STUDY DESIGN AND

METHODS:

Data were collected from 754 virus validation studies (individual data points) by Plasma Protein Therapeutics Association member companies and analyzed for the capacity of a range of nanofilters to remove viruses with different physicochemical properties and sizes. Different plasma product intermediates were spiked with viruses and filtered through nanofilters with different pore sizes using either tangential or dead-end mode under constant pressure or constant flow. Filtration was performed according to validated scaled-down laboratory conditions reflecting manufacturing processes. Effectiveness of viral removal was assessed using cell culture infectivity assays or polymerase chain reaction (PCR).

RESULTS:

The nanofiltration process demonstrated a high efficacy and robustness for virus removal. The main factors affecting nanofiltration efficacy are nanofilter pore size and virus size. The capacity of nanofilters to remove smaller, nonenveloped viruses was dependent on filter pore size and whether the nanofiltration process was integrated and designed with the intention to provide effective parvovirus retention. Volume filtered, operating pressure, and total protein concentration did not have a significant impact on the effectiveness of virus removal capacity within the investigated ranges.

CONCLUSIONS:

The largest and most diverse nanofiltration data collection to date substantiates the effectiveness and robustness of nanofiltration in virus removal under manufacturing conditions of different plasma-derived proteins. Nanofiltration can enhance product safety by providing very high removal capacity of viruses including small non-enveloped viruses.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Plasma / Vírus / Proteínas Sanguíneas / Ultrafiltração Limite: Humans Idioma: En Revista: Transfusion Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Suíça

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Plasma / Vírus / Proteínas Sanguíneas / Ultrafiltração Limite: Humans Idioma: En Revista: Transfusion Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Suíça