1985
DOI: 10.1046/j.1537-2995.1985.25686071422.x
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Inactivation of viruses in labile blood derivatives. I. Disruption of lipid‐enveloped viruses by tri(n‐butyl)phosphate detergent combinations

Abstract: Use of the organic solvent, tri(n-butyl)phosphate (TNBP), and detergents for the inactivation of viruses in labile blood derivatives was evaluated by addition of marker viruses (VSV, Sindbis, Sendai, EMC) to anti-hemophilic factor (AHF) concentrates. The rate of virus inactivation obtained with TNBP plus Tween 80 was superior to that observed with ethyl ether plus Tween 80, a condition previously shown to inactivate greater than or equal to 10(6.9) CID50 of hepatitis B and greater than or equal to 10(4) CID50 … Show more

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Cited by 333 publications
(156 citation statements)
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“…FCV, a non-enveloped virus, has a capsid that consists of a protein and lacks an envelope that surrounds it. Although enveloped viruses are effectively eliminated by solvent/detergent treatment, non-enveloped viruses are not affected by this treatment [44]. Non-enveloped viruses, without a lipid coat, are resistant to most of the viral inactivation methods that have been described to date [45,46].…”
Section: Virucidal Activity Of Photocatalysis By Tio 2 -Coated Glassmentioning
confidence: 99%
“…FCV, a non-enveloped virus, has a capsid that consists of a protein and lacks an envelope that surrounds it. Although enveloped viruses are effectively eliminated by solvent/detergent treatment, non-enveloped viruses are not affected by this treatment [44]. Non-enveloped viruses, without a lipid coat, are resistant to most of the viral inactivation methods that have been described to date [45,46].…”
Section: Virucidal Activity Of Photocatalysis By Tio 2 -Coated Glassmentioning
confidence: 99%
“…From the mid-1980s to the early 1990s, heat treatment of freeze-dried coagulation factors at 60-68°C for 24-96 h or 80°C for 72 h were developed to inactivate HIV and HCV concomitantly [156]. Although pasteurization has successfully been adapted to several plasma products (such as antithrombin and alpha 1-antitrypsin), a milestone in the safety of industrial plasma products was the development of the solvent/detergent (S/D) incubation procedure at 20-37°C [157] designed to dissolve the lipid envelope of viruses, including HCV, without affecting plasma protein functions. This technique is still largely used for a wide range of industrial plasma products owing to wellproven efficacy and a safety profile established by years of industrial and clinical practices [158].…”
Section: Hcv Reduction Treatment Of Industrial Plasma Protein Productsmentioning
confidence: 99%
“…A 30 kD Millipore Pellicon Systen was used to perform diafiltration and protein level adjustment. Virus inactivation was performed using a solvent (tri-n-butyl phosphate; TNBP) and a detergent (Tween 80) (Horowitz et al, 1985). To remove the solvent and detergent, a cation-exchange chromatography using a CM Sepharose FF stationary phase was performed.…”
Section: Immunoglobulin Fractionationmentioning
confidence: 99%