Method for detecting hepatitis B surface antigen with inductively coupled plasma mass spectrometry
A technology of hepatitis B surface antigen and inductive coupling, applied in the field of mass spectrometry, can solve the problems of limited selection of markers, narrow detection range, radiation hazards, etc., and achieve the effect of excellent accuracy, rapid detection, and wide linear range
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Embodiment 1
[0022] A kind of ICP-MS detection method based on the HBsAg of ZnSe colloidal solution labeling antibody, it comprises the steps:
[0023] 1) Preparation of ZnSe colloidal solution:
[0024] Preparation: refer to the literature [Enustun. B. V, Turkevich. J. J. Am. Chem. Soc . 1963, 85, 3317-3328], specifically: measure 125mL of twice distilled water and fill it with nitrogen to remove oxygen for 1 h, then add 0.875g (2.35 mmol) ZnClO to the water under stirring conditions 4 ·6H 2 O and 5.7 mmol of MPA (used as a stabilizer), adjust the pH value of the reaction solution to 6.5 with 1 mol / L NaOH solution, and continue to pass nitrogen gas into the solution to remove oxygen. With stirring, add 0.134 g (0.46 mmol) Al 2 Se 3 and excess sulfuric acid to react (to produce fresh H 2 Se 3 ), in this state, the precursor of ZnSe was produced. Then heated to reflux for 2 h, after the nucleation and growth stages, a ZnSe colloidal solution was obtained.
[0025] Purification: r...
Embodiment 2
[0034] A kind of ICP-MS detection method based on the HBsAg of nano-gold colloid solution labeling antibody, it comprises the steps:
[0035] 1) Preparation of nano-gold colloidal solution:
[0036] Preparation: Refer to literature [B. Nikoobakht, M.A. El-Sayed, Chem. Mater., 2003, 15, 1957-1962, A. Gole, C.J. Murphy, Chem. r., 2005, 17, 1325-1330] to synthesize nano-gold colloidal solution by promoting the growth process of seed crystals. The main process is: 5 mL of 0.2 mol / L cetyltrimethylammonium bromide (CTAB) and 5 mL of 0.5 mmol / L HAuCl 4 Mix, add 0.6 mL ice NaBH with a concentration of 0.01 mol / L under stirring 4 The solution was stirred vigorously for 2 min. At this time, the solution was brownish-yellow. Then, it was placed in a 25°C water bath for about 2 h to obtain a gold seed solution.
[0037] Dissolve 3.4624 g CTAB in 95 mL of water, and add 1 mL of 0.01 mol / L AgNO under stirring 3 solution, and then slowly add 0.6 mL of ascorbic acid (AA) solution wi...
Embodiment 3
[0046] Detection of clinical samples:
[0047] 10 serum samples were collected from the hospital, and tested according to the methods described in Examples 1 and 2, respectively. Calculate the corresponding concentration according to the linear equation, calculate the concentration of the antigen in the serum, and then compare it with the results obtained by the enzyme-linked immunoassay used in clinical diagnosis in the hospital. The results are shown in Table 1. In enzyme-linked immunoassay, if the normal value of HBsAg (ng / ml) is greater than or equal to 0.5 ng / mL, it is regarded as a positive result (+), otherwise it is regarded as a negative result (-). It can be seen from Table 1 that the detection results obtained according to the methods of the two embodiments are basically consistent with the traditional clinical detection results, indicating that the detection method of the present invention can meet the clinical needs for HBsAg detection.
[0048]
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