发明名称 |
METHOD FOR DOSING THE CONTROL CAPACITY OF C1INH |
摘要 |
The present invention relates to a method for dosing the control capacity of plasma serpin (SERine Protease INhibitor) C1 inhibitor (C1Inh) on the basis of a patient blood sample. The invention also relates to a kit specially designed for said dosing. |
申请公布号 |
US2014315232(A1) |
申请公布日期 |
2014.10.23 |
申请号 |
US201214358887 |
申请日期 |
2012.11.28 |
申请人 |
UNIVERSITE JOSEPH FOURIER (GRENOBLE 1) ;CENTRE HOSPITALIER UNIVERSITAIRE DE GRENOBLE |
发明人 |
Drouet Christian;Ghannam Arije;Defendi Federica;Favier Bertrand |
分类号 |
C12Q1/37 |
主分类号 |
C12Q1/37 |
代理机构 |
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代理人 |
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主权项 |
1. A method for dosing the control capacity of the protein C1 plasma inhibitor (C1Inh) based on a sample of plasma from a patient, comprising the following steps:
a) a reaction mixture is prepared based on prekallikrein (pKK), high molecular weight kininogen (HK) and activated Hageman factor protease (FXIIa), the reaction mixture being adjusted in such a manner as to have a pH higher than 7; b) the plasma sample of the patient is incubated with a serine protease inhibitor for a duration at least equal to 5 minutes, in such a manner as to obtain a plasma sample without spontaneous protease activity and in which said inhibitor is inactivated or becomes inactive with regard to the reaction mixture prepared at step a); c) the plasma sample obtained at step b) is incubated with the reaction mixture prepared at step a) for a duration lower than or equal to 20 minutes; d) a chromogenic or fluorogenic substrate of the kallikrein (KK), liable to release a chromophore or a fluorophore after hydrolysis by KK, is added to the plasma sample obtained at step c); e) the possible release of the chromophore or fluorophore obtained at step d) is detected over time; and f) the control capacity of C1Inh is determined based on the detection achieved at step e). |
地址 |
Grenoble FR |