Hepatitis B virus adsorbent as well as preparation method and application thereof
A hepatitis B virus and adsorbent technology, applied in the field of biomedical adsorption materials, can solve the problems of high cost of antibodies, high immunogenicity of antibodies, and long time, and achieve the effects of specific affinity, long storage period, and high adsorption efficiency
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[0029] The invention provides a kind of preparation method of hepatitis B virus adsorbent, comprises the steps:
[0030] S1, washing the carboxylated agarose gel microspheres to obtain an agarose gel microsphere suspension;
[0031] S2, placing the amino-modified nucleic acid aptamer in the aptamer dissolving buffer, shaking and dissolving, performing a water bath treatment, and then placing it in a room temperature environment, and obtaining the dissolved aptamer after renaturation;
[0032] S3, N-hydroxysuccinimide and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride are mixed according to the preset molar ratio and dissolved in 2-(N- Morpholine) in ethanesulfonic acid buffer solution, obtain cross-linking catalyst;
[0033] S4. Add the cross-linking catalyst obtained in step S3 into the agarose gel suspension obtained in step S1, mix well, then add the dissolved aptamer obtained in step S2, and perform amide reaction;
[0034] S5. After the amide reaction in st...
Embodiment 1
[0043] This embodiment provides a kind of preparation method of hepatitis B virus adsorbent, its reaction principle is as follows figure 1 As shown, it specifically includes the following steps:
[0044] S1. Shake and mix the carboxylated agarose gel microspheres, use a pipette gun to extract 10mL of the mixed microspheres, transfer them to a 100mL Erlenmeyer flask, let stand at room temperature for 5min, slowly absorb and discard the upper layer Protect buffer, add 30mL distilled water to resuspend, transfer to a suction filter flask, use 200mL distilled water to wash three times to completely remove part of the protection buffer, and quickly transfer the washed microspheres to a 100mL Erlenmeyer flask, the whole process makes The microspheres were kept wet, resulting in an agarose gel microsphere suspension.
[0045] S2. Take out the EP tube containing 250 μg of amino-modified nucleic acid aptamers from the refrigerator at -20°C, let it stand at room temperature for 5 minut...
Embodiment 2~10
[0050] Embodiments 2 to 10 respectively provide a preparation method of a hepatitis B virus adsorbent. Compared with Example 1, the difference is that the molar ratio of NHS and EDC in step S3 or the reaction time in step S4 are changed, The molar ratios and reaction times corresponding to each embodiment are shown in Table 1.
[0051] The reaction parameters corresponding to Table 1 Embodiment 2~10
[0052]
[0053]
[0054] Get the static blood sample from the hepatitis B patient, respectively adopt the hepatitis B virus adsorbent prepared in embodiment 1~10, according to the ratio of adsorbent:blood=1:5, the blood sample is adsorbed, and the hepatitis B surface in the sample before and after adsorption Antigen content was detected. Among them, the content of hepatitis B surface antigen in the sample before adsorption was 66.29IU / mL, and the content of hepatitis B surface antigen obtained after adsorption with the hepatitis B virus adsorbents provided in Examples 1-10...
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