US4285933A
Expired / Lapsed
US
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Process for concentrating blood coagulation Factor XIII derived from human placentae
Assignee: Tanabe Pharma Corp
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Filing: 1979-11-02
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Granted: 1981-08-25
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Expires: 1999-11-02
Abstract
Abstract The invention relates to a process for concentrating blood coagulation Factor XIII (Fibrin stabilizing factor) which comprises removing a fraction precipitated at a pH of 6 to 9 in a concentration of 4 to 9% (W/V) of an alkylenoxide polymer or copolymer having a molecular weight of 2,000 to 20,000 from a crude globulin fraction obtained from human placentae by separating in albumin fraction therefrom, and then collecting the fraction precipitated in the concentration of 20 to 30% (W/V) of said polymer or copolymer, thereby obtaining easily said blood coagulation Factor XIII free from pyrogen in good yield.
Inventors
- 👤 Tunekazu Fukushima
- 👤 Satoshi Funakoshi
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-10-23 15:06
CPC Classifications
C; C12; C12N; C12N9/00; C12N9/10; C12N9/1025; C12N9/104; C12N9/1044; A; A61; A61K; A61K31/00; A61K31/13; A61K31/14; A61K35/00; A61K35/12; A61K35/14; A61L; A61L2/00; A61L2/02; A61L2/022; A61L2/04; A61K38/00; A61L2103/00; A61L2103/05; A61L2103/09
Claims Analysis
Total Claims: 2
Claim 1
Independent Claim
288 words
A process for concentrating a blood coagulation Factor XIII derived from human placentae consisting essentially of (1) recovering an extract with a physiologically saline solution from human placentae, (2) removing precipitate from the solution by centrifugation, (3) adding ammonium sulfate to the supernatant in a concentration of 20 to 30% (W/V), (4) recovering the supernatant and removing the precipitate therefrom, (5) adding ammonium sulfate to the supernatant in a concentration of 45 to 55% (W/V) to recover precipitate, (6) dissolving the precipitate into a phosphate buffer solution of pH 6 to 9 containing about 0.005 M of EDTA, (7) adding alkylene-oxide polymer of copolymer having a molecular weight of 2,000 to 20,000 which is selected from the group consisting of polyethylene oxide homopolymer, polypropylene oxide homopolymer and ethylene oxidepropylene oxide copolymer in a concentration of 4 to 0% W/V, (8) removing the formed precipitate and recovering the supernatant, (9) adding the above-mentioned alkylene-oxide polymer or copolymer to the supernatant in a concentration of 20 to 30% (W/V), (10) recovering the precipitate formed and dissolving it into a phosphate buffer of pH 6 to 9, (11) heat-treating the collected precipitate for 9 to 11 hours at 55° to 65° C. in an aqueous solution of a neutral amino acid, monosaccharide, sugar alcohol or a mixture of two or more thereof in a concentration of 10 to 20% (W/V) thereby to inactivate hepatitis virus, (12) contacting the resulting solution with a DEAE-crosslinked dextran which had been equilibrated to pH of 6 to 9 thereby to absorb blood coagulation Factor XIII, (13) eluting the blood coagulation Factor XIII with an about 0.05 M phosphate buffer containing about 0.5 M NaCl, (14) subjecting the collected eluate to dialysis, sterilizing filtration and freeze-drying.
Claim 2
Dependent Claim
288 words
A process for concentrating a blood coagulation Factor XIII derived from human placentae consisting essentially of (1) recovering an extract with a physiologically saline solution from human placentae, (2) removing precipitate from the solution by centrifugation, (3) adding ammonium sulfate to the supernatant in a concentration of 20 to 30% (W/V), (4) recovering the supernatant and removing the precipitate therefrom, (5) adding ammonium sulfate to the supernatant in a concentration of 45 to 55% (W/V) to recover precipitate, (6) dissolving the precipitate into a phosphate buffer solution of pH 6 to 9 containing about 0.005 M of EDTA, (7) adding alkylene-oxide polymer of copolymer having a molecular weight of 2,000 to 20,000 which is selected from the group consisting of polyethylene oxide homopolymer, polypropylene oxide homopolymer and ethylene oxidepropylene oxide copolymer in a concentration of 4 to 0% W/V, (8) removing the formed precipitate and recovering the supernatant, (9) adding the above-mentioned alkylene-oxide polymer or copolymer to the supernatant in a concentration of 20 to 30% (W/V), (10) recovering the precipitate formed and dissolving it into a phosphate buffer of pH 6 to 9, (11) heat-treating the collected precipitate for 9 to 11 hours at 55° to 65° C. in an aqueous solution of a neutral amino acid, monosaccharide, sugar alcohol or a mixture of two or more thereof in a concentration of 10 to 20% (W/V) thereby to inactivate hepatitis virus, (12) contacting the resulting solution with a DEAE-crosslinked dextran which had been equilibrated to pH of 6 to 9 thereby to absorb blood coagulation Factor XIII, (13) eluting the blood coagulation Factor XIII with an about 0.05 M phosphate buffer containing about 0.5 M NaCl, (14) subjecting the collected eluate to dialysis, sterilizing filtration and freeze-drying.
References Cited (Backward Citations)
US3880989A
Cited
JPS5359018A
Cited
USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1984-08-24 | 1985-02-23 | 1985-08-25 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1988-08-24 | 1989-02-23 | 1989-08-25 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1992-08-24 | 1993-02-23 | 1993-08-25 | $7700.00 | Window Closed / Lapsed |