Carboxymethyl-hydroxypropyl-beta-cyclodextrin and preparation method thereof
A technology of cyclodextrin and carboxymethyl, which is applied in the field of carboxymethyl-hydroxypropyl-β-cyclodextrin and its preparation, can solve the problems of limited practicability, high dosage of prescription auxiliary materials, influence on cyclodextrin and the like, To achieve the effect of appropriate drug inclusion ability, low production cost and enhanced absorption
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Embodiment 1
[0062] The three-necked round-bottomed flask is equipped with a constant pressure funnel, a reflux condenser, and a thermometer. Add 50ml of pure water into it, start stirring, and then slowly add 0.02mol β-cyclodextrin (22.7g) and 0.3mol solid NaOH (12.0g) under successive stirring. ), the system was dissolved and then heated slowly to keep at 80°C, then slowly added 0.08mol ethyl chloroacetate (9.8g) dropwise for about 4 hours, continued to stir and reflux for 2 hours and then cooled to room temperature. Control the temperature in the water bath <20°C, slowly add 0.14mol of 1,2-propylene oxide (8.1g) dropwise to the system under stirring, and finish adding in about 3 hours, continue to stir and react for 5 hours under the condition of water bath temperature <20°C, add hydrochloric acid to adjust pH to neutral, filter, pour the filtrate into a dialysis bag, and dialyze to remove residual β-cyclodextrin and 1,2-propanediol and glycolic acid (sodium) produced by the reaction. C...
Embodiment 2
[0069] Add 50ml of pure water to a three-neck round bottom flask equipped with a constant pressure funnel, reflux condenser, and thermometer, start stirring, and then slowly add 0.02mol β-cyclodextrin (22.7g) and 0.14mol solid NaOH (12.0g) in sequence After the system is dissolved, control the temperature of the water bath to 1 HNMR verifies that the average degree of substitution of carboxymethyl is 2.1, and the average degree of substitution of hydroxypropyl is 5.8. The product is abbreviated as CM 2 -HP 6 -β—CD.
Embodiment 3
[0071] It is basically the same as Example 1, but wherein the feeding amounts of NaOH, ethyl chloroacetate, and 1,2-propylene oxide are respectively 0.22, 0.04, and 0.05 mol. Finally, the product yield is 98.5%. 1 HNMR verifies that the average substitution degree of carboxymethyl group is 1.2, and the average substitution degree of hydroxypropyl group is 1.8. The product is abbreviated as CM 1 -HP 2 -β—CD.
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