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Method for removing human immunodeficiency virus and/or its related compounds

Assignee: Kuraray Co Ltd
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Filing: 1988-11-29
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Granted: 1991-08-20
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Expires: 2008-11-29
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Abstract

Abstract The present invention provides removing agents comprising a solid substance with a weakly acidic or weakly alkaline surface. Since the removing agents can be used for treating body fluid of a patient by, for example, extra-corporeal circulation system thereby effectively removing human immunodeficiency virus and/or its related compounds contained in the body fluid, it is expected that the life of the patient could be prolonged. The significance of the present invention therefore is great.

Inventors

  • 👤 Seisuke Takashima
  • 👤 Keiichi Kurokawa
  • 👤 Shuhei Nakaji
  • 👤 Ken Yamane
  • 👤 Ryosuke Murayama

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-09 02:00
CPC Classifications
B; B01; B01D; B01D15/00; A; A61; A61M; A61M1/00; A61M1/34; A61M1/3472; A61M1/3486; B01J; B01J39/00; B01J39/04; B01J39/07; A61M1/36; A61M1/3679; A61M2202/00; A61M2202/20; A61M2202/206; Y; Y10; Y10S; Y10S128/00; Y10S128/03

Claims Analysis

Total Claims: 8
Claim 1
Independent Claim 50 words
A method for removing human immunodeficiency virus, its related compounds, or a combination thereof from body fluids of patients comprising the step of contacting said body fluids with a solid carrier of a 3-component calcinated product of hydroxyapatite-silica-alumina wherein said solid carrier has a pH ranging from 2.5 to 6.9.
Claim 2
Independent Claim 50 words
A method for removing human immunodeficiency virus, its related compounds, or a combination thereof from body fluids of patients comprising the step of contacting said body fluids with a solid carrier of a 3-component calcinated product of hydroxyapatite-silica-alumina wherein said solid carrier has a pH ranging from 2.5 to 6.9.
Claim 3
Independent Claim 86 words
A method for removing immunodeficiency virus, its related compounds, or a combination thereof from body fluids of patients comprising the steps of: (a) passing blood taken from a patient in need of such treatment through a column packed with a solid carrier of a 3-component calcinated product of hydroxyapatite-silica-alumina, wherein said solid carrier has a pH ranging from 2.5 to 6.9 to remove human immunodeficiency virus, its related compounds, or a combination thereof, thereby cleansing said blood; and (b) administering said cleansed blood to the patient.
Claim 4
Independent Claim 86 words
A method for removing immunodeficiency virus, its related compounds, or a combination thereof from body fluids of patients comprising the steps of: (a) passing blood taken from a patient in need of such treatment through a column packed with a solid carrier of a 3-component calcinated product of hydroxyapatite-silica-alumina, wherein said solid carrier has a pH ranging from 2.5 to 6.9 to remove human immunodeficiency virus, its related compounds, or a combination thereof, thereby cleansing said blood; and (b) administering said cleansed blood to the patient.
Claim 5
Independent Claim 106 words
A method for removing human immunodeficiency virus, its related compounds or a combination thereof from body fluids of patients comprising the steps of: (a) separating contaminated blood taken from a patient in need of such treatment into hemocytes and plasma; (b) passing said plasma through column packed with a solid carrier of a 3-component calcinated product of hydroxyapatite-silica-alumina, wherein said solid carrier has a pH ranging from 2.5 to 6.9 to remove human immunodeficiency virus, its related compounds or both, thereby cleansing said plasma; (c) combining said cleansed plasma with hemocytes to form cleansed whole blood; and (d) returning said cleansed whole blood to said patient.
Claim 6
Independent Claim 106 words
A method for removing human immunodeficiency virus, its related compounds or a combination thereof from body fluids of patients comprising the steps of: (a) separating contaminated blood taken from a patient in need of such treatment into hemocytes and plasma; (b) passing said plasma through column packed with a solid carrier of a 3-component calcinated product of hydroxyapatite-silica-alumina, wherein said solid carrier has a pH ranging from 2.5 to 6.9 to remove human immunodeficiency virus, its related compounds or both, thereby cleansing said plasma; (c) combining said cleansed plasma with hemocytes to form cleansed whole blood; and (d) returning said cleansed whole blood to said patient.
Claim 7
Dependent Claim 14 words
The method according to claim 3, wherein said contaminated blood is separated by centrifugation.
Claim 8
Dependent Claim 16 words
The method according to claim 3, wherein said contaminated blood is separated via a separation membrane.

References Cited (Backward Citations)

US3925152A Cited
US3963613A Cited
GB2006642A Cited
JPS54135497A Cited
US4215688A Cited
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US4681870A Cited
JPS61226058A Cited
JPS62266072A Cited
EP0263934A1 Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1994-08-19 1995-02-18 1995-08-20 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1998-08-19 1999-02-18 1999-08-20 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 2002-08-19 2003-02-18 2003-08-20 $7700.00 Window Closed / Lapsed

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