Antiheparin serum total bilirubin (vanadate oxidation method) detection kit
A detection kit and a technology for total bilirubin, applied in the field of serum total bilirubin detection reagents, can solve problems such as inaccurate detection results, troubles in popularization and use, and abnormal detection results, so as to improve clarity and accuracy degree, the effect of improving specificity
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Embodiment 1
[0036] Disodium hydrogen phosphate-benzoic acid buffer (pH2.9) 0.1mol / L
[0037] Fatty alcohol polyoxyethylene ether 5g / L-10 g / L
[0038] Alkylphenol polyoxyethylene ether (OP) 4 g / L -8g / L
[0039] Polyethylene glycol 8000 1%-5.0%
[0040] Triton-305 2.5 g / L - 5g / L
[0041] Sodium fluoride 1.0g / L-2.0 g / L
[0042] Tetrasodium EDTA 1g / L-2 g / L
[0043] Reagent R2:
[0044] Phosphate buffer (pH7.0) 10mmol / L
[0045] Disodium EDTA 5g / L-10g / L
[0046] Tetrasodium EDTA 1g / L-2g / L
[0047] Sodium metavanadate 4mmol / L
[0048] The usage method of this embodiment reagent:
[0049] The serum total bilirubin (vanadate oxidation method) detection reagent described in this embodiment adopts a fully automatic biochemical analyzer during use, such as Hitachi 7180 fully automatic analyzer, etc., and utilizes a two-point endpoint method for determination. Set the ratio of sample and reagent to 9:240:60, the detection wavelength is 450nm, place distilled water, standard and sample in th...
Embodiment 2
[0051] Interference test: Take fresh mixed serum, divide it into 2 equal parts, then divide each equal part into 5 equal parts, add different interfering substances, so that the concentration in the serum reaches Figure 4 requirements. Then respectively use the reagent obtained in Example 1 to compare and measure the content of serum total cholesterol with the common and recognized serum total cholesterol reagent in the market simultaneously. The measurement results of the control group and the measurement results of each group after adding different interfering substances are shown in Figure 4 . Relative deviation (%) = (measuring mean value of interference samples - measuring mean value of control samples) / measured mean value of control samples × 100%.
[0052] Depend on Figure 4 It can be seen that the conditions of ascorbic acid ≤ 20mmol / L, heparin ≤ 0.5%, hemoglobin ≤ 200mg / L, and triglyceride ≤ 22.6mmol / L did not significantly interfere with the test results of the ...
Embodiment 3
[0054] Correlation experiment: use the formula of Example 1 to prepare reagents, and conduct a control test with the serum total bilirubin (vanadate oxidation method) kit of a company approved by the State Food and Drug Administration, which is common in the market, and detect 20 samples simultaneously. Clinical serum samples, test results such as Figure 5 shown. And obtained the correlation curve of the two reagents (such as figure 1 As shown), the test results show that the correlation coefficient of the two kits is 0.999, indicating that there is a great correlation between the two.
[0055] The calibrators and quality controls used in the test were:
[0056] Calibrator: RANDOX926 serum total bilirubin content is 32.2 μmol / L.
[0057] Quality control: RANDOX1005 serum total cholesterol target value is 29.3 μmol / L, target value range: 23.2~35.4 μmol / L.
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