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US4093606A Expired / Lapsed US ⏱️ 0.0 years remaining

Method of producing intravenously injectable gamma globulin and a gamma globulin suitable for carrying out the method

Assignee: Individual
•
Filing: 1976-05-21
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Granted: 1978-06-06
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Expires: 1996-05-21
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Abstract

Abstract A process is provided for the preparation of a gamma globulin suitable for intravenous administration from the readily available Fraction II or II + III plasma protein paste. The Fraction II or II + III paste is extracted with water at a pH of 4.8 - 6.5 and impurities are fractionally precipitated by addition of polyethylene glycol to 4% of wt./vol. and then 5% wt./vol. The desired gamma globulin is then precipitated at a pH 8.0 by addition of polyethylene glycol to 12% wt./vol.

Inventors

  • 👤 Myer Louis Coval

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-25 19:51
CPC Classifications
C; C07; C07K; C07K16/00; C07K16/06; Y; Y10; Y10S; Y10S530/00; Y10S530/827; Y10S530/829; Y10S530/83; Y10S530/831

Claims Analysis

Total Claims: 7
Claim 1
Independent Claim 137 words
A process for preparing a gamma globulin substantially devoid of anticomplementary activity and suitable for intravenous administration, from a material selected from the Fraction II + III plasma protein paste having a protein content of about 25-30% and Fraction II paste which comprises the steps: a. suspending said paste in water to form a solution of low ionic strength having a conductance of about 300 × 10 -6 cm -6 ohm -1 at a pH of about 4.8 to 6.5 to produce a precipitate and filtrate, b. fractionally precipitating impurities from said filtrate by adding polyethylene glycol to 4% weight/volume and then 5% weight/volume, c. precipitating the gamma globulin by adding polyethylene glycol to 12% weight/volume at a pH of about 8.0. said process being carried out at a temperature of about 0° to 20 ° C.
Claim 2
Dependent Claim 137 words
A process for preparing a gamma globulin substantially devoid of anticomplementary activity and suitable for intravenous administration, from a material selected from the Fraction II + III plasma protein paste having a protein content of about 25-30% and Fraction II paste which comprises the steps: a. suspending said paste in water to form a solution of low ionic strength having a conductance of about 300 × 10 -6 cm -6 ohm -1 at a pH of about 4.8 to 6.5 to produce a precipitate and filtrate, b. fractionally precipitating impurities from said filtrate by adding polyethylene glycol to 4% weight/volume and then 5% weight/volume, c. precipitating the gamma globulin by adding polyethylene glycol to 12% weight/volume at a pH of about 8.0. said process being carried out at a temperature of about 0° to 20 ° C.
Claim 3
Dependent Claim 20 words
A process according to claim 1 wherein the pH at which the paste is extracted is about 5.7 to 5.9.
Claim 4
Dependent Claim 27 words
A process according to claim 2 wherein 1 kg. of Fraction II + III paste is extracted at pH 5.8 with about 30 liters of pyrogen-free water.
Claim 5
Dependent Claim 19 words
A process according to claim 1 wherein the polyethylene glycol has a molecular weight of about 4,000 to 6,000.
Claim 6
Dependent Claim 17 words
A process according to claim 4 wherein the polyethylene glycol has a molecular weight of about 4,000.
Claim 7
Dependent Claim 21 words
A process according to claim 5 wherein the process is carried out at a temperature of about 0° to 5° C.

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1981-06-05 1981-12-05 1982-06-06 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1985-06-05 1985-12-05 1986-06-06 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1989-06-05 1989-12-05 1990-06-06 $7700.00 Window Closed / Lapsed

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