A kind of trimethoprim hapten and its colloidal gold detection device and its preparation method
A trimethoprim and detection device technology, which is applied in the field of trimethoprim hapten and its colloidal gold detection device and its preparation, can solve the problem of high technical requirements for operators, complex safety regulations of instruments and equipment, and inability to display results immediately, etc. problem, to achieve the effect of high detection sensitivity, easy production and high accuracy
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Embodiment 1
[0042] The preparation of the trimethoprim hapten was prepared by the following steps:
[0043] In a 100mL three-necked flask, 2.5g of trimethoprim and 30mL of 48% by mass hydrobromic acid were sequentially added, reacted at 100°C for 3 hours, and then quenched by adding 6mL of 50% by mass sodium hydroxide solution. After the crystals were precipitated by cooling, the crystals were then dissolved in 20 mL of boiling water, and then concentrated ammonia water was added to adjust the pH to 7, followed by recrystallization and purification.
[0044] Take 0.5g of the crystal from the previous step and dissolve it in 10ml of DMF, add 0.5g of potassium carbonate, and 0.43mL of bromopropionic acid, and react at 40°C for 6 hours. Ethyl acetate extraction and column purification to obtain trimethoprim hapten.
[0045] The obtained trimethoprim hapten is detected, MASS[M+H] is 349.2, such as figure 1 Shown; its melting point is 214 degrees.
Embodiment 2
[0047] Using trimethoprim hapten to prepare the synthesis of trimethoprim immune antigen, the following steps are used to prepare:
[0048] Dissolve 0.1 mmol of trimethoprim hapten in 2 mL of DMF, and add 27.5 mg of DCC and 14.4 mg of NHS with stirring. Magnetic stirring was carried out overnight at 4°C. After centrifugation, the supernatant was liquid A, and 140 mg of human serum albumin (KLH) was weighed and dissolved in 10 mL of PBS with a concentration of 0.1 mol / L and a pH of 8.0. Add DMF 1mL, stir and dissolve to prepare solution B, under magnetic stirring, gradually drop solution A into solution B, and react at 4°C for 12h. After centrifugation, the supernatant was taken, dialyzed with normal saline at 4°C for 3 days, and the dialysate was changed 3 times a day. The obtained whole antigen was dispensed into 0.5 mL centrifuge tubes at a concentration of 1 mg / mL, and frozen in a -20°C refrigerator.
Embodiment 3
[0050] Using trimethoprim to immunize antigen to prepare trimethoprim monoclonal antibody, adopt the following steps to prepare:
[0051] Use trimethoprim to immunize the antigen and identify and immunize four 6-week-old Kunming mice. After boosting the immunization three times, blood is collected to measure the titer. When the serum titer no longer rises, the mice are immunized with twice the dose of the antigen without adjuvant , three days later, the mice were killed by neck dislocation, the spleen was taken under aseptic conditions to prepare splenocytes, and the vigorously growing mouse myeloma cells were mixed in a 50mL centrifuge tube at a ratio of 8:1, and 30mL of serum-free IPMI1640 was added to culture Base, centrifuge at 1100r / min for 5 minutes, discard the supernatant, shake the cell mass gently, and place it in a water bath at 37 degrees Celsius. Slowly add 1 mL of 50% PEG-4000 by volume to the cells, drop it within 1 minute, and at the same time gently stir the s...
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