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YAN Chen, XIONG Keqiang, WANG Wenji, LI Ling. Inactivation and validation of virus in blood products of human coagulation factor Ⅷ[J]. Journal of Pharmaceutical Practice and Service, 2014, 32(3): 199-202. doi: 10.3969/j.issn.1006-0111.2014.03.009
Citation: YAN Chen, XIONG Keqiang, WANG Wenji, LI Ling. Inactivation and validation of virus in blood products of human coagulation factor Ⅷ[J]. Journal of Pharmaceutical Practice and Service, 2014, 32(3): 199-202. doi: 10.3969/j.issn.1006-0111.2014.03.009

Inactivation and validation of virus in blood products of human coagulation factor Ⅷ

doi: 10.3969/j.issn.1006-0111.2014.03.009
  • Received Date: 2013-03-05
  • Rev Recd Date: 2013-06-19
  • Objective To study effect of virus inactivation/removal treated by solvent/detergent method and dry heating at 80℃, 72 h for inactivation in human coagulation factor Ⅷ. Methods Human coagulation factor Ⅷ extracted from healthy human plasma were treated by solvent/detergent method and dry heating at 80℃, 72 h for inactivation. The virus inactivation effect was validated by adding the indicator virus ( PRV, Sindbis, HIV, EMCV, PPV). Results The methods could effectively inactivate lipid-enveloped and non lipid-enveloped viruses which could be used for virus inactivation/removal during human coagulation factor Ⅷ experiments, the residual amount of TNBP in production was less than one percent ten thousand(10 ppm), the residual Tween-80 concentration was less than one percent hundred thousand(100 ppm),which all met the safety standards. Conclusion and no significant change was observed in the activation and other indicators of human coagulation factor Ⅷ.
  • [1] 刘隽湘. 输血疗法与血液制剂[M].北京: 人民卫生出版社, 1996: 214-215.
    [2] Brackmann HH, Oldenburg J, Eis-Hubinger AM, et al. Hepatitis A virus infection among the hemophiliapopulation at the Bonn Hemophilia Center[J]. Vox Sang,1994, 67(S1): 3-8.
    [3] Mannucci PM, Gdovin S, Gringeri A, et al. Transmission of hepatitis A to patients with hemophilia by factor Ⅷ concentrates treated with organic solvent and detergent to inactivate viruses. The Italian Collaborative Group[J].Ann Intern Med,1994, 120(1): 1-7.
    [4] Lawlor E, Johnson Z, Thornton L, et al. Investigation of an outbreak of hepatitis A in Irish haemophilia A patients[J].Vox Sang 1994,67(S1): 18-20.
    [5] Soucie JM, Robertson BH, Bell BP, et al. Hepatitis A virus infections associated with clotting factor concentrate in the United States[J].Transfusion,1998, 38(6): 573-579.
    [6] Aguilar FC, Lucia CJF, Ferrer TJ, et al. Parvovirus B19 infection in patients with congenital blood coagulation disorders[J].Med Clin,1997, 108(17): 641-646.
    [7] Santagostino E, Mannucci PM, Gringeri A, et al. Transmission of parvovirus B19 by coagulation factor concentrates exposed to 100 degrees C heat after lyophilization[J].Transfusion,1997, 37(5): 517-522.
    [8] Lefrere JJ, Mariotti M, Thauvin M. B19 parvovirus DNA in solvent/detergent-treated anti-haemophilia concentrates[J].Lancet,1994, 343(8891): 211-212.
    [9] Azzi A, Ciappi S, Zakvrzewska K, et al. Human parvovirus B19 infection in hemophiliacs first infused with two high-purity, virally attenuated factor Ⅷ concentrates[J]. Am J Hematol,1992, 39: 228-230.
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Inactivation and validation of virus in blood products of human coagulation factor Ⅷ

doi: 10.3969/j.issn.1006-0111.2014.03.009

Abstract: Objective To study effect of virus inactivation/removal treated by solvent/detergent method and dry heating at 80℃, 72 h for inactivation in human coagulation factor Ⅷ. Methods Human coagulation factor Ⅷ extracted from healthy human plasma were treated by solvent/detergent method and dry heating at 80℃, 72 h for inactivation. The virus inactivation effect was validated by adding the indicator virus ( PRV, Sindbis, HIV, EMCV, PPV). Results The methods could effectively inactivate lipid-enveloped and non lipid-enveloped viruses which could be used for virus inactivation/removal during human coagulation factor Ⅷ experiments, the residual amount of TNBP in production was less than one percent ten thousand(10 ppm), the residual Tween-80 concentration was less than one percent hundred thousand(100 ppm),which all met the safety standards. Conclusion and no significant change was observed in the activation and other indicators of human coagulation factor Ⅷ.

YAN Chen, XIONG Keqiang, WANG Wenji, LI Ling. Inactivation and validation of virus in blood products of human coagulation factor Ⅷ[J]. Journal of Pharmaceutical Practice and Service, 2014, 32(3): 199-202. doi: 10.3969/j.issn.1006-0111.2014.03.009
Citation: YAN Chen, XIONG Keqiang, WANG Wenji, LI Ling. Inactivation and validation of virus in blood products of human coagulation factor Ⅷ[J]. Journal of Pharmaceutical Practice and Service, 2014, 32(3): 199-202. doi: 10.3969/j.issn.1006-0111.2014.03.009
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