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US4185964A Expired / Lapsed US ⏱️ 0.0 years remaining

Lysing reagent

Assignee: Central Laboratories of Associated Maryland Pathologists Ltd
•
Filing: 1977-02-08
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Granted: 1980-01-29
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Expires: 1997-02-08
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Abstract

Abstract Azide-free blood diluents and cyanide ion-free erythrocyte lysing reagentshich are particularly advantageous for use with Coulter scanning devices. The lysing reagent comprises (1) a water-soluble quaternary ammonium salt of the formula R 1 N(R 2 ) 3 X wherein R 1 is a 12-20 C alkyl, each R 2 is the same or different and is lower alkyl or lower hydroxyalkyl and X is an anion, and (2) a minor amount of a water-soluble polycarboxylic acid.

Inventors

  • 👤 Robert G. Lancaster

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-24 00:13
CPC Classifications
G; G01; G01N; G01N33/00; G01N33/48; G01N33/50; G01N33/96; G01N33/5005; G01N33/5094; Y; Y10; Y10T; Y10T436/00; Y10T436/10; Y10T436/101666; Y10T436/107497; Y10T436/108331

Claims Analysis

Total Claims: 23
Claim 1
Independent Claim 102 words
A lysing reagent for lysing erythrocytes while leukocytes remain substantially intact and forming chromogens with hemoglobin comprising a cyanide ion-free aqueous solution containing a minor amount sufficient for erythrocytolysis and forming chromogens with hemoglobin of a water-soluble quaternary ammonium salt of the formula R.sub.1 N(R.sub.2).sub.3 X wherein R 1 is an alkyl having about 12 to 20 carbon atoms, each R 2 is the same or different and is lower alkyl or lower hydroxyalkyl, and X is an anion; and a minor amount sufficient to inhibit leukocytolysis of a water-soluble polycarboxylic acid, or salt thereof, of up to about 8 carbon atoms.
Claim 2
Dependent Claim 102 words
A lysing reagent for lysing erythrocytes while leukocytes remain substantially intact and forming chromogens with hemoglobin comprising a cyanide ion-free aqueous solution containing a minor amount sufficient for erythrocytolysis and forming chromogens with hemoglobin of a water-soluble quaternary ammonium salt of the formula R.sub.1 N(R.sub.2).sub.3 X wherein R 1 is an alkyl having about 12 to 20 carbon atoms, each R 2 is the same or different and is lower alkyl or lower hydroxyalkyl, and X is an anion; and a minor amount sufficient to inhibit leukocytolysis of a water-soluble polycarboxylic acid, or salt thereof, of up to about 8 carbon atoms.
Claim 3
Dependent Claim 26 words
The lysing reagent of claim 1 wherein the quaternary ammonium salt is selected from the group consisting of a halide, sulfate, phosphate, or a nitrate salt.
Claim 4
Dependent Claim 19 words
The lysing reagent of claim 2 wherein the polycarboxylic acid or salt is a hydroxy-containing polycarboxylic acid or salt.
Claim 5
Dependent Claim 15 words
The lysing reagent of claim 3 wherein the polycarboxylic salt is an alkali metal salt.
Claim 6
Dependent Claim 32 words
The lysing reagent of claim 3 wherein in the quaternary ammonium salt, R 1 has about 14 to 18 carbon atoms and R 2 is alkyl of 1 to 3 carbon atoms.
Claim 7
Dependent Claim 17 words
The lysing reagent of claim 3 wherein the reagent further comprises a minor amount of lower alkanol.
Claim 8
Dependent Claim 15 words
The lysing agent of claim 6 wherein the polycarboxylic acid salt is sodium potassium tartrate.
Claim 9
Dependent Claim 15 words
The lysing reagent of claim 7 wherein the quaternary ammonium salt is cetyltrimethyl ammonium bromide.
Claim 10
Dependent Claim 33 words
The lysing reagent of claim 7 wherein in the quaternary ammonium salt, R 1 has about 14 to 18 carbon atoms and R 2 is alkyl of 1 to about 3 carbon atoms.
Claim 11
Dependent Claim 40 words
The lysing reagent of claim 9 comprising about 10 to 50 grams per liter cetyltrimethyl ammonium bromide; about 5 to 50 grams per liter sodium potassium tartrate; and about 5 to 100 milliliters of ethanol per liter of lysing reagent.
Claim 12
Dependent Claim 15 words
The lysing reagent of claim 10 wherein the quaternary ammonium salt is cetyltrimethyl ammonium bromide.
Claim 13
Dependent Claim 46 words
In a method for lysing erythrocytes and forming chromogens with hemoglobin while leukocytes remain substantially intact wherein a reagent is reacted with a blood sample for erythrocytolysis and for forming chromogens with hemoglobin, the improvement employing as the lysing reagent the lysing reagent of claim 1.
Claim 14
Dependent Claim 14 words
The method of claim 12 wherein the polycarboxylic salt comprises an alkali metal salt.
Claim 15
Dependent Claim 31 words
The method of claim 13 wherein in the quaternary ammonium salt, R 1 has about 14 to 18 carbon atoms and R 2 is alkyl of 1 to 3 carbon atoms.
Claim 16
Dependent Claim 25 words
The method of claim 12 wherein the quaternary ammonium salt is selected from the group consisting of a halide, sulfate, phosphate, or a nitrate salt.
Claim 17
Dependent Claim 31 words
The method of claim 15 wherein in the quaternary ammonium salt, R 1 has about 14 to 18 carbon atoms and R 2 is alkyl of 1 to 3 carbon atoms.
Claim 18
Dependent Claim 18 words
The method of claim 15 wherein the polycarboxylic acid or salt is a hydroxy-containing polycarboxylic acid or salt.
Claim 19
Dependent Claim 13 words
The method of claim 17 wherein the polycarboxylic salt is sodium potassium tartrate.
Claim 20
Dependent Claim 39 words
The method of claim 18 comprising about 10 to 50 grams per liter cetyltrimethyl ammonium bromide; about 5 to 50 grams per liter sodium potassium tartrate; and about 5 to 100 milliliters of ethanol per liter of lysing reagent.
Claim 21
Dependent Claim 16 words
The method of claim 15 wherein the reagent further comprises a minor amount of lower alkanol.
Claim 22
Dependent Claim 14 words
The method of claim 20 wherein the quaternary ammonium salt is cetyltrimethyl ammonium bromide.
Claim 23
Dependent Claim 14 words
The method of claim 21 wherein the quaternary ammonium salt is cetyltrimethyl ammonium bromide.

References Cited (Backward Citations)

US3874851A Cited
US3874852A Cited
US3874852B1 Cited
US4013417A Cited
US3977995A Cited
US3964865A Cited
US4030888A Cited
US4040785A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1983-01-28 1983-07-30 1984-01-29 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1987-01-28 1987-07-30 1988-01-29 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1991-01-28 1991-07-30 1992-01-29 $7700.00 Window Closed / Lapsed

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