Hematological assay and reagent
AssigneePentapharm AG
InventorsPatrizia Maria Gempeler, Andreas Calatzis
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AssigneePentapharm AG
InventorsPatrizia Maria Gempeler, Andreas Calatzis
Estimating the term…
A hematological assay is described in which the blood coagulation potential of a body fluid is assessed by reacting a sample of the body fluid with an amount of an activator reagent comprising: (a) a predetermined amount of factor Xa or a hematologically equivalent mutant thereof, and (b) a predetermined amount of factor Va, a hematologically equivalent mutant thereof or an enzyme activating endogenous factor V, (c) (optionally) phospholipids. The reagent may be dry (e.g. lyophilised) or in an aqueous solution preferably buffered to a pH from 6 to 10 (preferably 7 to 8), if desired incubating, if necessary inducing coagulation by the addition of one or more coagulation accelerants such as calcium chloride, and establishing a value indicative of the coagulation potential, e.g. by measuring the time to clotting on an optical coagulometer or through use of a chromogenic substrate. It is preferred to use at (b) factor V activator from purified Russell's Viper venom (RVV-V). An activator reagent is also described containing the components mentioned above preferably in one or more buffer solutions or in dried, e.g. lyophilised form.
A hematological assay in which the blood coagulation potential of a body fluid selected from whole or citrated (or equivalently stabilised) blood or plasma is assessed by reacting a sample of the body fluid with an activator reagent,
A point-of-care hematological assay in accordance with any preceding claim wherein a sample of activator reagent is positioned in one or more reaction locations in a test apparatus and a sample of body fluid to be assayed is applied at an inlet location in said apparatus and arranged to contact and react with the activator reagent, and a value is established indicative of the coagulation potential,
Dependencies are inferred from the claim text.