Hybridoma cell line of secreting meloxicam monoclonal antibodies and application thereof
a technology of meloxicam and monoclonal antibodies, which is applied in the field of hybridoma cell lines of secreting meloxicam monoclonal antibodies and application thereof, can solve the problems of cumbersome methods, time-consuming and expensive, and the inability to achieve rapid detection of a large number of samples, and achieve good specificity and detection sensitivity
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example 1
[0084]Synthesis of Meroxicam Hapten
[0085]The synthesis path is shown in FIG. 1.
[0086]1 g of compound 1 was dissolved in 50 ml of methanol solution, and stirred at 157° C. for the night after adding 157 mg MeONa, and then the compound 1 was gotten. 1.20 g of compound 2 was dissolved 30 ml DMF, and added 1.20 mg Ethyl 4-bromobutyrate stir at 80° C. for the night, and then the mixture 2 was gotten. The step 4 is to concentrate the obtained mixture 2 and then purify it with a silica gel column to obtain compound 3. The 800 mg compound 3 was dissolved into 3 mL tetrahydrofuran and 1 mL water, adding 180 mg 1-hydrated lithium hydroxide, adjusting pH to 4-6, and stirring at room temperature overnight to get mixture 4. The aqueous solution layer with ethylamine from mixture 4 was extracted, and the organic layer was combined, washing with salt water, drying with anhydrous sodium sulfate and being concentrated to obtain meloxicam hapten.
[0087]The products of compound 3 and haptens are calcul...
example 2
[0089]Complete Antigen Synthesis of Meloxicam
[0090]1.7 mg Melo, 2.2 mg 1-ethyl carbodiimine hydrochloride and 1.4 mg N-hydroxysuccinylimide was dissolved into 400 phenyl-anhydrous N, N-dimethylamine, stirring 6-8 h at room temperature to obtain A1 solution. 10 mg keyhole blood blue protein (KLH) (Melo to KLH Moore ratio of 1500:1) was diluted with an appropriate amount of boric acid buffer solution, and B1 solution was obtained. At room temperature, A1 solution was added to B1 solution one drop at a time. Complete antigen (Melo-KLH) is obtained by separating complete antigen and uncoupled small molecule hapten (Melo) by dialysis.
[0091]1.7 mg Melo, 2.2 mg 1-ethyl carbodiimine hydrochloride and 1.4 mg N-hydroxysuccinylimide was dissolved into 400 phenyl-anhydrous N, N-dimethylamine, stirring 6-8 h at room temperature to obtain A1 solution. 10 mg keyhole blood blue protein (KLH) (Melo to KLH Moore ratio of 3000:1) was diluted with an appropriate amount of boric acid buffer solution, an...
example 3
[0093]Synthesis of the Meroxicam Coating Antigen
[0094]1.8 mg Melo 2.4 mg 1-ethylenediamine hydrochloride salt 1.45 mg N-hydroxysuccinylimide was dissolved into 300 phenyl-anhydrous N, N-dimethylamine, and stir it 6-8 h at room temperature to obtain A2 solution. 5 mg of chicken egg albumin (OVA) was dissolved in 2 mL boric acid buffer solution to obtain B2 solution. At room temperature, A2 solution was added to B2 solution, and mixed solution was obtained after overnight reaction at room temperature. Complete antigens, uncoupled small molecule haptens (Melo) and coating antigen (Melo-OVA) were separated by dialysis.
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