Assay for low molecular weight heparin
View Patent ↗A prothrombin time reagent for determination of low molecular weight heparin in fresh whole blood and in anti-coagulant treated blood is provided. The reagent is composed of recombinant animal tissue factor, and a mixture of synthetic phospholipids, which mixture includes a phosphatidylalcohol. A formulation buffer which includes a sensitivity adjuster is used in formulating the reagent. The recombinant animal tissue factor includes rabbit brain. The synthetic phospholipids of the mixture include palmitoyloleoylphosphatidylcholine (POPC), palmitoyloleoyl-phosphatidylserine (POPS), and a phosphatidylalcohol. The phosphatidyl alcohol includes dioleoylphosphatidylethanol, dioleoylphosphatidylmethanol, dioleoylphosphatidylpropanol, dioleoylphosphatidylbutanol, and dioleoylphosphatidylinositol. The sensitivity adjuster included in the formulation buffer is γ-Cyclodextrin. The formulated reagent is air-dried and remains stable for at least 3 weeks at 37° C.
1. A method for preparing an air-dried prothrombin time reagent, comprising the steps of:
(A) providing a recombinant animal tissue factor;
(B) providing a mixture of synthetic phospholipids;
(C) selecting a phosphatidylalcohol;
(D) adding said selected phosphatidylalcohol to said mixture to form a lipid mixture, which composition is present in an effective amount to lipidate said recombinant animal tissue factor to form a lipidated tissue factor;
(E) combining said recombinant animal tissue factor with said lipid mixture to form a lipidated tissue factor solution;
(F) adding a formulation buffer solution comprising a sensitivity adjuster to said lipidated tissue factor solution to form a liquid reagent; and,
(G) drying said liquid reagent in an atmosphere of about 5% to about 10% relative humidity, and at about 20° C. to about 37° C. to form an air-dried reagent.
2. The method according to claim 1 , wherein the recombinant animal tissue factor of step (A) is derived from rabbit brain and is present in an amount of about 4 μg/ml to about 6 μg/ml.
3. The method according to claim 1 , wherein the step of providing a mixture further comprises providing a mixture of palmitoyloleoylphosphatidylcholine (POPC) and palmitoyoleoylphosphatidylserinc (POPS).
4. The method according to claim 3 ,where the step of selecting a phosphatidylalcohol further comprises the step of selecting said phosphatidylalcohol from the group consisting of: dioleoylphosphatidylethanol, dioleoylphosphatidylmethanol, dioleoylphosphatidylpropanol, dioleoylphosphatidylbutanol, and dioleoylphosphatidylinositol.
5. The method according to claim 3 , wherein said POPL, said POPS and said selected phosphatidylalcohol is present in a molar ratio of 70:15:15 or 70:20:10 or 70:10:20.
6. The method according to claim 5 , wherein the sensitivity adjuster comprises an aldehyde free gamma cyclodextrin, a derivative thereof, or an analog thereof.
7. The method according to claim 2 , wherein step (G) includes drying said liquid reagent for about two hours to provide a reagent that remains stable for at least three weeks at a temperature of about 37° C.