The present application relates to a preparation process of
nifedipine preparation, and belongs to the technical field of
drug synthesis. In the present application, PEG4000 and PEG1500 are compounded and used as a
solid dispersion carrier, and the main components are distributed in the carrier in a molecular state;
sodium carboxymethyl starch and
corn starch are selected as filling adjuvants, which can significantly improve the
dissolution effect of the raw
drug, reduce the adsorption of
nifedipine, cooperate with the
solid dispersion carrier, further eliminate the adsorption of the raw
drug molecules, improve the
dissolution degree of the drug, and the
dissolution speed is fast. The present application further improves the dissolution degree and dissolution rate of the prepared
nifedipine preparation, and more than 90% of the nifedipine preparation can be dissolved in 30 minutes, and finally the dissolution effect close to 100% is realized, and the
bioavailability of the drug is significantly improved.