High quality human immunoglobulin G purified from Cohn fractions by liquid chromatography

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Abstract

In order to obtain intravenous immunoglobulin G (iv IgG) of high quality from F-I+II+III or F-II+III pastes prepared by the Cohn method, we developed a chromatography process using ion exchange gels, Q-Sepharose FF and CM-Sepharose FF, and Sephacryl S-300 gel filtration. Viral inactivation was performed by incubating the preparation with pepsin at pH 4.0 at 35°C for 18 h. The characteristics of 28 batches produced by us were: yield 4.3 ± 0.2 g/l plasma, i.e., a recovery of 39.1 ± 1.8%; IgG subclasses distribution: IgG1 = 58.4%, IgG2 = 34.8%, IgG3 = 4.5% and IgG4 = 2.3%; IgG size distribution was 98.4% monomers, 1.2% dimers and 0.4% polymers and protein aggregates; anticomplement activity was less than 0.5 CH50/mg IgG, and prekallikrein activator activity (PKA) was less than 5 IU/ml. These characteristics satisfied the requirements of the European Pharmacopoea edition, and the regulations of the Brazilian Health Ministry (M.S. Portaria No. 2, 30/10/1998).

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Tanaka, K., Sawatani, E., Dias, G. A., Shigueoka, E. M., Campos, T. C. X. B., Nakao, H. C., & Arashiro, F. (2000). High quality human immunoglobulin G purified from Cohn fractions by liquid chromatography. Brazilian Journal of Medical and Biological Research, 33(1), 27–30. https://doi.org/10.1590/S0100-879X2000000100004

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