Diagnostic test utilizing human chorionic gonadotropin

Claim 2

In a test method suitable for the detection of the human chorionic gonadotropin of pregnancy or cancer in urine at a concentration as low as about 40 m.I.U./ml of urine and capable of detecting pregnancy as early as day 26 of a regular 28 day menstrual cycle including: (a) clarifying a sample of the urine to be tested; (b) subjecting about 5 to 50 ml of the clarified urine sample to absorbent induced ultrafiltration through a ultrafiltration membrane backed by a layer of absorbent capable of sorbing urine serum passing through the membrane, and said membrane having a molecular weight cut-off from about 15,000 to about 35,000, whereby human chorionic gonadotropin is retained in the sample; (c) continuing the ultrafiltration until the retentate sample is one-tenth to one-five hundredth its original volume; (d) diluting the retentate with sufficient water to provide a retentate sample of about 0.5 ml; and (e) contacting the retentate sample with the appropriate amount of an immunologic reagent for detecting the presence of human chorionic gonadotropin in the retentate sample; the improvement which comprises contacting said membrane with a dilute solution of polyvinylpyrrolidone prior to or concurrent with ultrafiltration, wherein said polyvinylpyrrolidone has an average molecular weight greater than about 9,000 and less than about 40,000; and wherein said immunologic reagent comprises: (1) pyruvic aldehyde stabilized erythrocytes sensitized to human chorionic gonadotropin with a bifunctional molecule selected from glutaraldehyde, glyoxal, succinialdehyde, hexamethylene diisocyanate, toluene 2,4-diisocyanate, diethylmalonimidate dihydrochloride, dimethyl suberimidate, bis diazotized benzidine, cyanuric chloride, tetrazotized o-anisidine, and 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide; and (2) a highly purified antiserum to human chorionic gonadotropin or the beta subunit thereof.

Claim 3

The method of claim 1, wherein the average molecular weight of said polyvinylpyrrolidone is about 33,000.

Claim 4

The method of claim 2, wherein the concentration of the dilute solution of polyvinylpyrrolidone is from about 0.5% to about 4.0%, weight by volume.

Claim 5

The method of claim 3, wherein said concentration is from about 1.0% to about 2.0%, weight by volume.

Claim 6

The method of claim 4 wherein said bifunctional molecule is selected from glutaraldehyde and hexamethylene diisocyante, and said highly purified antiserum is adjusted to have a sensitivity to human chorionic gonadotropin of about 100-150 m.I.U. per test and a cross reactivity to other glycoprotein hormone antigens of less than 25%.

Claim 7

The method of claim 1, wherein the average molecular of said polyvinylpyrrolidone is from about 28,000 to about 35,000.

Claim 8

The method of claim 6, wherein the concentration of the dilute solution of polyvinylpyrrolidone is from about 0.5% to about 4.0%, weight by volume.

Claim 9

The method of claim 7, wherein said concentration is from about 1.0% to about 2.0%, weight by volume.

Claim 10

The method of claim 7 wherein said bifunctional molecule is selected from glutaraldehyde and hexamethylene diisocyanate, and said highly purified antiserum is adjusted to have a sensitivity to human chorionic gonadotropin of about 100-150 m.I.U. per test and a cross reactivity to other glycoprotein hormone antigens of less than 25%.

Claim 11

In a test method suitable for the detection of the human chorionic gonadotropin of pregnancy or cancer in urine at a concentration as low as about 40 m.I.U./ml of urine and capable of detecting pregnancy as early as day 26 of a regular 28 day menstrual cycle including: (a) clarifying a sample of the urine to be tested; (b) subjecting about 5 to 50 ml of the clarified urine sample to absorbent induced ultrafiltration through a ultrafiltration membrane backed by a layer of absorbent capable of sorbing urine serum passing through the membrane, and said membrane having a molecular weight cut-off from about 15,000 to about 35,000, whereby human chorionic gonadotropin is retained in the sample; (c) continuing the ultrafiltration until the retentate sample is one-tenth to one-five hundredth its original volume; (d) diluting the retentate with sufficient water to provide a retentate sample of about 0.5 ml; and (e) contacting the retentate sample with the appropriate amount of an immunologic reagent fo detecting the presence of human chorionic gonadotropin in the retentate sample; the improvement which comprises pre-washing said membrane with about a 0.5% to about 4.0% solution of polyvinylpyrrolidone prior to ultrafiltration, wherein said polyvinylpyrrolidone has an average molecular weight greater than about 9,000 and less than about 40,000; and wherein said immunologic reagent comprises: (1) pyruvic aldehyde stabilized erythrocytes sensitized to human chorionic gonadotropin with a bifunctional molecular selected from glutaraldehyde, glyoxal, succinialdehyde, hexamethylene diisocyanate, toluene 2,4diisocyanate, diethylmalonimidate dihydrochloride, dimethyl suberimidate, bis diazotized benzidine, cyanuric chloride, tetrazotized o-anisidine, and 1-ethyl-3-(3-dimethylaminiopropyl) carbodiimide; and (2) a highly purified antiserum to human chorionic gonadotropin or the beta subunit thereof.

Claim 12

In a test method suitable for the detection of the human chorionic gonadotropin of pregnancy or cancer in urine at a concentration as low as about 40 m.I.U./ml of urine and capable of detecting pregnancy as early as day 26 of a regular 28 day menstrual cycle including: (a) clarifying a sample of the urine to be tested; (b) subjecting about 5 to 50 ml of the clarified urine sample to absorbent induced ultrafiltration through a ultrafiltration membrane backed by a layer of absorbent capable of sorbing urine serum passing through the membrane, and said membrane having a molecular weight cut-off from about 15,000 to about 35,000, whereby human chorionic gonadotropin is retained in the sample; (c) continuing the ultrafiltration until the retentate sample is one-tenth to one-five hundredth its original volume; (d) diluting the retentate with sufficient water to provide a retentate sample of about 0.5 ml; and (e) contacting the retentate sample with the appropriate amount of an immunologic reagent fo detecting the presence of human chorionic gonadotropin in the retentate sample; the improvement which comprises pre-washing said membrane with about a 0.5% to about 4.0% solution of polyvinylpyrrolidone prior to ultrafiltration, wherein said polyvinylpyrrolidone has an average molecular weight greater than about 9,000 and less than about 40,000; and wherein said immunologic reagent comprises: (1) pyruvic aldehyde stabilized erythrocytes sensitized to human chorionic gonadotropin with a bifunctional molecular selected from glutaraldehyde, glyoxal, succinialdehyde, hexamethylene diisocyanate, toluene 2,4diisocyanate, diethylmalonimidate dihydrochloride, dimethyl suberimidate, bis diazotized benzidine, cyanuric chloride, tetrazotized o-anisidine, and 1-ethyl-3-(3-dimethylaminiopropyl) carbodiimide; and (2) a highly purified antiserum to human chorionic gonadotropin or the beta subunit thereof.

Claim 13

The method of claim 10 wherein the ultrafiltration membrane is of the anisotropic type; the average molecular weight of the polyvinylpyrrolidone is from about 20,000 to about 35,000; and the concentration of said solution of polyvinylpyrrolidone is from about 1.0% to about 2.0%, weight by volume.

Claim 14

The method of claim 11 wherein said clarifying step comprises filtration through a filter; the average molecular weight of the polyvinylpyrrolidone is about 33,000; and which further comprises prewashing said filter with the aqueous solution of polyvinylpyrrolidone.

Claim 15

The method of claim 12 wherein said bifunctional molecule is selected from glutaraldehyde and hexamethylene diisocyante, and said highly purified antiserum is adjusted to have a sensitivity to human chorionic gonadotropin of about 100-150 m.I.U. per test and a cross reactivity to other glycoprotein hormone antigens of less than 25%.

Claim 16

In a test method suitable for the detection of the human chorionic gonadotropin of pregnancy or cancer in urine at a concentration as low as about 40 m.I.U./ml of urine and capable of detecting pregnancy as early as day 26 of a regular 28 day menstrual cycle including: (a) clarifying a sample of the urine to be tested through a filter; (b) subjecting about 5 to 50 ml of the clarified urine sample to absorbent induced ultrafiltration through a ultrafiltration membrane backed by a layer of absorbent capable of sorbing urine serum passing through the membrane, and said membrane having a molecular weight cut-off from about 15,000 to about 35,000, whereby human chorionic gonadotropin is retained in the sample; (c) continuing the ultrafiltration until the retentate sample is one-tenth to one-five hundredth its original volume; (d) diluting the retentate with sufficient water to provide a retentate sample of about 0.5 ml; and (e) contacting the retentate sample with the appropriate amount of an immunologic reagent for detecting the presence of human chorionic gonadotropin in the retentate sample; the improvement which comprises pretreating said filter with about a 0.5% to about 4.0% solution of polyvinylpyrrolidone prior to ultrafiltration, wherein said polyvinylpyrrolidone has an average molecular weight greater than about 9,000 and less than about 40,000; and wherein said immunologic reagent comprises: (1) pyruvic aldehyde stabilized erythrocytes sensitized to human chorionic gonadotropin with a bifunctional molecule selected from glutaraldehyde, glyoxal, succinialdehyde, hexamethylene diisocyanate, toluene 2,4-diisocyanate, diethylmalonimidate dihydrochloride, dimethyl suberimidate, bis diazotized benzidine, cyanuric chloride, tetrazotized o-anisidine, and 1-ethyl-3-(3-dimethylaminopropyl)c carbodiimide; and (2) a highly purified antiserum to human chorionic gonadotropin or the beta subunit thereof.

Claim 17

In a test method suitable for the detection of the human chorionic gonadotropin of pregnancy or cancer in urine at a concentration as low as about 40 m.I.U./ml of urine and capable of detecting pregnancy as early as day 26 of a regular 28 day menstrual cycle including: (a) clarifying a sample of the urine to be tested through a filter; (b) subjecting about 5 to 50 ml of the clarified urine sample to absorbent induced ultrafiltration through a ultrafiltration membrane backed by a layer of absorbent capable of sorbing urine serum passing through the membrane, and said membrane having a molecular weight cut-off from about 15,000 to about 35,000, whereby human chorionic gonadotropin is retained in the sample; (c) continuing the ultrafiltration until the retentate sample is one-tenth to one-five hundredth its original volume; (d) diluting the retentate with sufficient water to provide a retentate sample of about 0.5 ml; and (e) contacting the retentate sample with the appropriate amount of an immunologic reagent for detecting the presence of human chorionic gonadotropin in the retentate sample; the improvement which comprises pretreating said filter with about a 0.5% to about 4.0% solution of polyvinylpyrrolidone prior to ultrafiltration, wherein said polyvinylpyrrolidone has an average molecular weight greater than about 9,000 and less than about 40,000; and wherein said immunologic reagent comprises: (1) pyruvic aldehyde stabilized erythrocytes sensitized to human chorionic gonadotropin with a bifunctional molecule selected from glutaraldehyde, glyoxal, succinialdehyde, hexamethylene diisocyanate, toluene 2,4-diisocyanate, diethylmalonimidate dihydrochloride, dimethyl suberimidate, bis diazotized benzidine, cyanuric chloride, tetrazotized o-anisidine, and 1-ethyl-3-(3-dimethylaminopropyl)c carbodiimide; and (2) a highly purified antiserum to human chorionic gonadotropin or the beta subunit thereof.

Claim 18

The method of claim 14 wherein the ultrafiltration membrane is of the anisotropic type; the average molecular weight of the polyvinylpyrrolidone is from about 20,000 to about 35,000; and the concentration of said solution of polyvinylpyrrolidone is from about 1.0% to about 2.0%, weight by volume.

Claim 19

The method of claim 15 wherein the average molecular weight of the polyvinylpyrrolidone is about 33,000.

Claim 20

The method of claim 16 wherein said bifunctional molecule is selected from glutaraldehyde and hexamethylene diisocyanate, and said highly purified antiserum is adjusted to have a sensitivity to human chorionic gonadotropin of about 100-150 m.I.U. per test and a cross reactivity to other glycoprotein hormone antigens of less than 25%.

Claim 21

The method of claim 17 wherein the ultrafiltration membrane is of the anisotropic type, the average molecular weight of the polyvinylpyrrolidone is from about 28,000 to about 35,000; and the concentration of the polyvinylpyrrolidone in the urine is from about 0.1% to about 1.0%, weight by volume.

Claim 22

In a test method suitable for the detection of the human chorionic gonadotropin of pregnancy or cancer in urine at a concentration as low as about 40 m.I.U./ml of urine and capable of detecting pregnancy as early as day 26 of a regular 28 day menstrual cycle including: (a) clarifying a sample of the urine to be tested; (b) subjecting about 5 to 50 ml of the clarified urine sample to absorbent induced ultrafiltration through a ultrafiltration membrane backed by a layer of absorbent capable of sorbing urine serum passing through the membrane, and said membrane having a molecular weight cut-off from about 15,000 to about 35,000, whereby human chorionic gonadotropin is retained in the sample; (c) continuing the ultrafiltration until the retentate sample is one-tenth to one-five hundredth its original volume; (d) diluting the retentate with sufficient water to provide a retentate sample of about 0.5 ml; and (e) contacting the retentate sample with the appropriate amount of an immunologic reagent for detecting the presence of human chorionic gonadotropin in the retentate sample; the improvement which comprises contacting said urine sample before or after clarification with a sufficient amount of polyvinylpyrrolidone to give a concentration of the polyvinylpyrrolidone in the urine of from about 0.01% to about 2.0%, wherein said polyvinylpyrrolidone has an average molecular weight greater than about 9,000 and less than about 40,000; and wherein said immunologic reagent comprises: (1) pyruvic aldehyde stabilized erythrocytes sensitized to human chorionic gonadotropin with a bifunctional molecule selected from glutaraldehyde, glyoxal, succinialdehyde, hexamethylene diisocyanate, toluene 2,4-diisocyanate, diethylmalonimidate dihydrochloride, dimethyl suberimidate, bis diazotized benzidine, cyanuric chloride, tetrazotized o-anisidine, and 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide; and (2) a highly purified antiserum to human chorionic gonadotropin or the beta subunit thereof.

Claim 23

In a test method suitable for the detection of the human chorionic gonadotropin of pregnancy or cancer in urine at a concentration as low as about 40 m.I.U./ml of urine and capable of detecting pregnancy as early as day 26 of a regular 28 day menstrual cycle including: (a) clarifying a sample of the urine to be tested; (b) subjecting about 5 to 50 ml of the clarified urine sample to absorbent induced ultrafiltration through a ultrafiltration membrane backed by a layer of absorbent capable of sorbing urine serum passing through the membrane, and said membrane having a molecular weight cut-off from about 15,000 to about 35,000, whereby human chorionic gonadotropin is retained in the sample; (c) continuing the ultrafiltration until the retentate sample is one-tenth to one-five hundredth its original volume; (d) diluting the retentate with sufficient water to provide a retentate sample of about 0.5 ml; and (e) contacting the retentate sample with the appropriate amount of an immunologic reagent for detecting the presence of human chorionic gonadotropin in the retentate sample; the improvement which comprises contacting said urine sample before or after clarification with a sufficient amount of polyvinylpyrrolidone to give a concentration of the polyvinylpyrrolidone in the urine of from about 0.01% to about 2.0%, wherein said polyvinylpyrrolidone has an average molecular weight greater than about 9,000 and less than about 40,000; and wherein said immunologic reagent comprises: (1) pyruvic aldehyde stabilized erythrocytes sensitized to human chorionic gonadotropin with a bifunctional molecule selected from glutaraldehyde, glyoxal, succinialdehyde, hexamethylene diisocyanate, toluene 2,4-diisocyanate, diethylmalonimidate dihydrochloride, dimethyl suberimidate, bis diazotized benzidine, cyanuric chloride, tetrazotized o-anisidine, and 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide; and (2) a highly purified antiserum to human chorionic gonadotropin or the beta subunit thereof.

Claim 24

The method of claim 19, wherein the average molecular weight of the polyvinylpyrrolidine is about 33,000.