Medicinal composition and preparation method thereof
A composition and medicine technology, applied in the field of pharmaceutical compositions and their preparation, can solve problems such as poor water solubility of medicines, and achieve the effects of convenient operation process, good solubility, and improved utilization efficiency
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[0043] According to the preparation method provided by the present invention, the contacting in step (a) is carried out under an inert atmosphere, and the contacting conditions include: the molar ratio of the ester to the cyclodextrin is 1-15:1, relatively For 1g of cyclodextrin, the amount of the organic amine is 0.01-5ml, the amount of the first organic solvent is 4-100ml, the contact temperature is 70-85°C, and the contact time is 10-15 hours.
[0044] Since lactide, glycolide and caprolactone are ring-opened under the action of the catalyst, they can directly react with -OH on the cyclodextrin. Therefore, in the present invention, one or both of lactide, glycolide and caprolactone are directly contacted with cyclodextrin to obtain the cyclodextrin-aliphatic polyester graft represented by formula (6). branch polymer. Lactide, glycolide, and caprolactone used in the present invention are all commercially available.
[0045] According to the preparation method provided by t...
Embodiment 1
[0065] Preparation of hydroxypropyl β-cyclodextrin-polylactic acid-dipalmitoylphosphatidylethanolamine grafted polymer nanoparticles loaded with paclitaxel
[0066] (1) Put 5.64g of lactide (Alfar Aesar, 97%, analytically pure) and 2.5g of hydroxypropyl β-cyclodextrin (Sigma-Aldrich, Japan) in a three-necked flask, and vacuumize for 1 hour Finally, add 10 mL of distilled dimethyl sulfoxide to dissolve, add 0.5 mL of triethylamine (Xilong Chemical Factory, Shantou City, Guangdong, analytically pure), and react at 80 °C for 12 hours under nitrogen protection to obtain hydroxypropyl β - Cyclodextrin-polylactic acid graft polymer crude product. Then precipitate with 200mL water, wash with water (100mL×4 times), dry in a vacuum oven at 20°C for 48 hours, then extract with toluene (20mL×2 times), and dry in a vacuum oven at 20°C for 48 hours. 6.11 g of solid product hydroxypropyl β-cyclodextrin-polylactic acid graft polymer was obtained. Calculated n=14.
[0067](2) Add 2 g of hy...
Embodiment 2
[0083] Preparation of hydroxypropyl β-cyclodextrin-polylactic acid-dipalmitoylphosphatidylethanolamine grafted polymer nanoparticles loaded with paclitaxel
[0084] Steps (1) to (3) were carried out according to the method of Example 1. The dosages, conditions and results of the substances involved in the method are shown in Tables 1 to 3.
[0085] (4) Dissolve 20 mg of purified hydroxypropyl β-cyclodextrin-polylactic acid-dipalmitoylphosphatidylethanolamine graft polymer in 3 mL of dichloromethane to obtain cyclodextrin-aliphatic polyester-phosphatidyl Ethanolamine-grafted polymer solution, 0.2 mg of paclitaxel (Norui Pharmaceutical Technology Co., Ltd., Beijing, batch number: 090328) was dissolved in 0.2 mL of dichloromethane to obtain paclitaxel solution, cyclodextrin-aliphatic polyester-phosphatidylethanolamine The graft polymer solution and paclitaxel solution were mixed, and the mixture was added to 20mL aqueous solution containing 0.4%wt surfactant polyvinyl alcohol (PV...
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