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Last Updated: April 25, 2024

Claims for Patent: 3,974,269


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Summary for Patent: 3,974,269
Title: Radioimmune assay method for detection of gonorrhea antibodies
Abstract:Gonorrhea antibodies in serum are detected by determination of radioactivity of conjugate formed between antibodies and antigens labelled with radioactive isotope.
Inventor(s): Maley; Frank (Delmar, NY)
Assignee: Research Corporation (New York, NY)
Application Number:05/487,971
Patent Claims:1. A radioimmunoassay method for determining the presence of Neisserria gonorrhoeae antibodies in human serum which comprises the steps of:

A. adding anti-human IgG to the serum to be tested in a buffered aqueous medium,

B. thereafter adding a heat labile antigen which has been produced by a growth culture of Neisseria gonorrhoeae, isolated therefrom, and labelled with a detectable radioactive element,

C. incubating resulting mixture at from about 4.degree.C to 45.degree.C for from about 24 to 2 hours at a pH of from about 6.5 to 8.5 to form an antigen-antibody conjugate when said antibodies are present, and

D. determining the level of radioactivity as a measure of the presence of said antigen-antibody conjugate.

2. A method as in claim 1 wherein the radioactive element is .sup.125 I.

3. A radioimmunoassay method for determining the presence of Niesseria gonorrhoeae antibodies in human serum which comprises the steps of:

A. adding anti-human IgG to the serum to be tested in a buffered aqueous medium,

B. thereafter adding a heat labile antigen which has been produced by a growth culture of Neisseria gonorrhoeae, isolated therefrom, and labelled with a detectable radioactive element,

C. incubating resulting mixture at from about 4.degree.C to 45.degree.C for from about 24 to 2 hours at a pH of from about 6.5 to 8.5 to form an antigen-antibody conjugate when said antibodies are present,

D. filter resulting mixture through a filter which has been previously washed with a reagent selected from the group consisting of bovine serum albumin, human serum immunoglobulin, ovalbumin, and hemoglobin to separate said antigen-antibody conjugate, and

E. determining the level of radioactivity in resulting precipitate as a measure of the presence of said antigen-antibody conjugate.

4. A method as in claim 3 wherein the radioactive element is .sup.125 I.

5. A method as in claim 3 wherein the reagent utilized in Step D is bovine serum albumin.

6. A method as in claim 3 wherein the radioactive element is .sup.125 I and the reagent utilized in Step D is bovine serum albumin.

7. A radioimmunoassay method for determining the presence of Neisseria gonorrhoeae antibodies in human serum which comprises the steps of:

A. adding anti-human IgG to the serum to be tested in a buffered aqueous medium containing a reagent selected from the group consisting of bovine serum albumin, human serum immunoglobulin, ovalbumin, and hemoglobin,

B. thereafter adding a heat labile antigen which has been produced by a growth culture of Neisseria gonorrhoeae, isolated therefrom, and labelled with a detectable radioactive element together with bovine serum albumin,

C. incubating resulting mixture at from about 4.degree.C to 45.degree.C for from about 24 to 2 hours at a pH of from about 6.5 to 8.5 to form an antigen-antibody conjugate when said antibodies are present,

D. diluting resulting mixture with an aqueous buffer and centrifuging, and

E. determining the level of radioactivity in resulting precipitate as a measure of the presence of said antigen-antibody conjugate.

8. A method as in claim 7 wherein the reagent is bovine serum albumin.

9. A method as in claim 7 wherein the radioactive element is .sup.125 I.

10. A method as in claim 7 wherein the buffer is phosphate buffered saline.

11. A method as in claim 7 wherein the reagent is bovine serum albumin, the radioactive element is .sup.125 I and the buffer is phosphate buffered saline.

Details for Patent 3,974,269

Applicant Tradename Biologic Ingredient Dosage Form BLA Approval Date Patent No. Expiredate
Grifols Therapeutics Llc ALBUKED, PLASBUMIN-20, PLASBUMIN-25, PLASBUMIN-5 albumin (human) For Injection 101138 10/21/1942 ⤷  Try a Trial 2040-01-28
Baxalta Us Inc. BUMINATE, FLEXBUMIN albumin (human) Injection 101452 03/03/1954 ⤷  Try a Trial 2040-01-28
Csl Behring Ag ALBURX albumin (human) Injection 102366 07/23/1976 ⤷  Try a Trial 2040-01-28
Grifols Biologicals Llc ALBUTEIN albumin (human) Injection 102478 08/15/1978 ⤷  Try a Trial 2040-01-28
>Applicant >Tradename >Biologic Ingredient >Dosage Form >BLA >Approval Date >Patent No. >Expiredate

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