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36 Results Found

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  1. Inactivation and removal of Zika virus during manufacture of plasma‐derived medicinal products

    Author
    Blumel, J. et al
    Organization
    Paul-Ehrlich-Institut
    Publisher
    Transfusion 2017 (57) 790-796
    Year
    2017
    Access
    Open
  2. cGMP production and analysis of BG505 SOSIP.664, an extensively glycosylated, trimeric HIV‐1 envelope glycoprotein vaccine candidate

    Author
    Dey, A., et al
    Organization
    International AIDS Vaccine Initiative, Department of Microbiology and Immunology, et al
    Publisher
    Biotechnology and Bioengineering 2018 (115) 885–899
    Year
    2018
    Access
    Open
  3. Hepatitis E virus derived from different sources exhibits different behaviour in virus inactivation and/or removal studies with plasma derivatives

    Author
    Yunoki, M., et al
    Organization
    Japan Blood Products Organization
    Publisher
    Biologicals 44(5) 403-411
    Year
    2016
    Access
    Abstract Only
  4. Pathogen safety of a pasteurized four‐factor human prothrombin complex concentrate preparation using serial 20N virus filtration

    Author
    Nowak, T., et al
    Organization
    CSL Behring
    Publisher
    Transfusion 57(5) 1184-1191
    Year
    2017
    Access
    Open
  5. Pathogen Safety of a New Intravenous Immune Globulin 10% Liquid

    Author
    Radomski, K., et al
    Organization
    Octapharma Biopharmaceuticals GmbH
    Publisher
    BioDrugs (2017) 31: 125
    Year
    2017
    Access
    Open
  6. Evaluation of the virus clearance capacity and robustness of the manufacturing process for the recombinant factor VIII protein, turoctocog alfa

    Author
    Ellgaard, T., et al
    Organization
    Novo Nordisk A/S
    Publisher
    Protein Expression and Purification 129 (2017) 94-100
    Year
    2017
    Access
    Open
  7. Validation of the manufacturing process used to produce long-acting recombinant factor IX Fc fusion protein

    Author
    McCue, J., et al
    Organization
    Biogen
    Publisher
    Haemophilia 20(4): e327-e335
    Year
    2014
    Access
    Open
  8. BAY 81-8973, a full-length recombinant factor VIII: manufacturing processes and product characteristics

    Author
    Garger, S., et al
    Organization
    Bayer
    Publisher
    Haemophilia 23(2): e67-e78
    Year
    2017
    Access
    Open
  9. Manufacturing process used to produce long-acting recombinant factor VIII Fc fusion protein

    Author
    McCue, J., et al
    Organization
    Biogen
    Publisher
    Biologicals 43: 213–219
    Year
    2015
    Access
    Open
  10. Pathogen safety and characterisation of a highly purified human alpha1-proteinase inhibitor preparation

    Author
    Kee, S., et al
    Organization
    CSL Behring
    Publisher
    Biologicals 47: 25–32
    Year
    2017
    Access
    Open
  11. Validation and implementation of Planova™ BioEX virus filters in the manufacture of a new liquid intravenous immunoglobulin in China"

    Author
    Ma, S., et al.
    Organization
    Shandong Taibang Biological Products Co., Ltd. and Asahi Kasei Medical Co., Ltd.
    Publisher
    Biologicals 52 (2018) 37-43
    Year
    2018
    Access
    Abstract Only
  12. Characterizing the Impact of Pressure on Virus Filtration Processes and Establishing Design Spaces to Ensure Effective Parvovirus Removal

    Author
    Strauss, D., et al
    Organization
    Asahi Kasei Bioprocess America
    Publisher
    Biotechnology Process e-pub
    Year
    2017
    Access
    Open
  13. Effect of Hydrodynamic Forces on Virus Removal Capability of Planova™ Filters

    Author
    Yamamoto, A. et al.
    Organization
    Asahi Kasei Corporation
    Publisher
    AIChE Journal Vol.60, No.6 2286-2297
    Year
    2014
    Access
    Abstract Only
  14. Improved removal of viruslike particles from purified monoclonal antibody IgM preparation via virus filtration

    Author
    Maerz, H., et al.
    Organization
    University of Leipzig, Humboldt-University/Charite, Dr. Fooke Laboratorien GmbH, and Asahi Chemical Industries
    Publisher
    Nature Biotechnology 14: 651-652
    Year
    1996
    Access
    No Abstract
  15. Development, upscaling and validation of the purification process for human-cl rhFVIII (Nuwiq), a new generation recombinant factor VIII produced in a human cell-line

    Author
    Winge, S., et al.
    Organization
    Octapharma AB
    Publisher
    Protein Expression and Purification 115 (2015) 165–175
    Year
    2015
    Access
    Open
  16. Pathogen safety of intravenous Rh immunoglobulin liquid and other immune globulin products: Enhanced nanofiltration and manufacturing process overview

    Author
    Soluk, L., et al
    Organization
    Cangene Corporation and Baxter Healthcare Corporation
    Publisher
    American Journal of Therapeutics 15: 435-443
    Year
    2008
    Access
    Abstract Only
  17. Capacity of the manufacturing process of Flebogamma© DIF, a new human high purity intravenous immunoglobulin, to remove a TSE model-agent

    Author
    Diez, J. M., et al.
    Organization
    Instituto Grifols S. A.
    Publisher
    Biologicals 38: 670-674
    Year
    2010
    Access
    Abstract Only
  18. Virus removal from Factor IX by filtration: Validation of the integritytest and effect of manufacturing process conditions

    Author
    Roberts, P. L., et al.
    Organization
    Bio Products Laboratory
    Publisher
    Biologicals 38: 303-31010
    Year
    2010
    Access
    Abstract Only
  19. Viral safety of C1-inhibitor NF

    Author
    Terpstra, F. G., et al.
    Organization
    Sanquin Research and Landsteiner Laboratory of the Academic Medical Center of the University of Amsterdam and Sanquin Plasma Products
    Publisher
    Biologicals 35: 173-181
    Year
    2007
    Access
    Abstract Only
  20. Comparison of nanofiltration efficacy in reducing infectivity of centrifuged versus ultracentrifuged 263K scrapie-infected brain homogenates in "spiked" albumin solutions

    Author
    Cardone, F., et al.
    Organization
    Istituto Superiore di Sanità, CEA/DSV/iMETI/SEPIA and LFB
    Publisher
    Transfusion 52: 953–962
    Year
    2012
    Access
    Abstract Only
  21. Removal of small non-enveloped viruses by nanofiltration

    Author
    Yokoyama, T., et al.
    Organization
    Japanese Red Cross and Sapporo Medical University School of Medicine & Department of Microbiology
    Publisher
    Vox Sanguinis 86: 225–229
    Year
    2004
    Access
    Abstract Only
  22. Nanofiltration, a new specific virus elimination method applied to high-purity Factor IX and Factor XI concentrates

    Author
    Burnouf-Radosevich, M., et al.
    Organization
    Centre Régional de Transfusion Sanguine
    Publisher
    Vox Sanguinis 67: 132-138
    Year
    1994
    Access
    Abstract Only
  23. Prion removal by nanofiltration under different experimental conditions

    Author
    Yunoki, M., et al.
    Organization
    Osaka University, Benesis Corporation, Mitsubishi Pharma Corporation, and Invitrogen BioServices
    Publisher
    Biologicals 36: 27-36
    Year
    2008
    Access
    Abstract Only
  24. Manufacturing process of Anti-thrombin III concentrate: viral safety validation studies and effect of column re-use on viral clearance

    Author
    Morrica, A., et al.
    Organization
    Kedrion S.p.A. and Q-ONE Biotech Ltd
    Publisher
    Biologicals 31: 165-173
    Year
    Access
    Abstract Only
  25. Phage passage after extended processing in small-virus-retentive filters

    Author
    Lute, S., et al.
    Organization
    Food and Drug Administration and Eli Lilly and Company
    Publisher
    Biotechnol. Appl. Biochem. 47: 141-151
    Year
    2007
    Access
    Abstract Only
  26. Large-scale production and properties of human plasma-derived activated Factor VII concentrate

    Author
    Tomokiyo, K., et al.
    Organization
    Kaketsuken
    Publisher
    Vox Sanguinis 84: 54-64
    Year
    2003
    Access
    Abstract Only
  27. In vitro study of a triple-secured von Willebrand factor concentrate

    Author
    Mazurier, C., et al.
    Organization
    Laboratoire Francais du Franctionnement et des Biotechnologies
    Publisher
    Vox Sanguinis 86: 100-104
    Year
    2004
    Access
    Abstract Only
  28. Implementation of a 20-nm pore-size filter in the plasma-derived Factor VIII manufacturing process

    Author
    Furuya, K., et al.
    Organization
    Japanese Red Cross Plasma Fractionation Center
    Publisher
    Vox Sanguinis 91: 119-125
    Year
    2006
    Access
    Abstract Only
  29. Removal of small nonenveloped viruses by antibody-enhanced nanofiltration during the manufacture of plasma derivative

    Author
    Kreil, T., et al.
    Organization
    Baxter BioScience
    Publisher
    Transfusion 46: 1143-1151
    Year
    2006
    Access
    Abstract Only
  30. Removal of small viruses (parvovirus) from IgG solution by virus removal filter Planova™ 20N

    Author
    Hongo, T., et al.
    Organization
    Asahi Kasei Medical Co., Ltd. and Yamaguchi University
    Publisher
    Journal of Membrane Science 278: 3-9
    Year
    2006
    Access
    Abstract Only
  31. A new liquid intravenous immunoglobulin with three dedicated virus reduction steps: virus and prion reduction capacity

    Author
    Poelsler, G., et al.
    Organization
    Baxter Bioscience
    Publisher
    Vox Sanguinis 94: 184-192
    Year
    2008
    Access
    Abstract Only
  32. Flebogamma© 5% DIF development: rationale for a new option in intravenous immunoglobulin therapy

    Author
    Jorquera, J. I.
    Organization
    Institute Grifols S.A.
    Publisher
    Clinical and Experimental Immunology 157: 17-21
    Year
    2009
    Access
    Open
  33. Effect of antibody solution conditions on filter performance for virus removal filter Planova™ 20N

    Author
    Hongo-Hirasaki, T., et al.
    Organization
    Asahi Kasei Medical Co., Ltd.
    Publisher
    Biotechnology Progress 26: 1080-1087
    Year
    2011
    Access
    Abstract Only
  34. Effects of varying virus-spiking conditions on a virus-removal filter Planova™ 20N in a virus validation study of antibody solutions

    Author
    Hongo-Hirasaki, T., et al.
    Organization
    Asahi Kasei Medical Co., Ltd.
    Publisher
    Biotechnology Progress 27: 162-169
    Year
    2011
    Access
    Abstract Only
  35. Effective virus inactivation and removal by steps of Biotest Pharmaceuticals IGIV production process

    Author
    Dichtelmuller H. O., et al.
    Organization
    Biotest AG and Biotest Pharmaceuticals
    Publisher
    Results in Immunology 2: 19-24
    Year
    2012
    Access
    Open
  36. Virus filtration of high-concentration monoclonal antibody solutions

    Author
    Marques, B., et al.
    Organization
    Merck and Co., Inc.
    Publisher
    Biotechnology Progress 25: 483-491
    Year
    2009
    Access
    Abstract Only