Method for preparing curcumin micelle with high medicine loading
A high drug loading, curcumin technology, applied in pharmaceutical formulations, medical preparations with inactive ingredients, antitumor drugs, etc., can solve the problems of low bioavailability and low drug loading in drug delivery systems, and achieve The effect of particle size and stability improvement, achieving synergistic therapeutic effect, and enhancing EPR effect
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Embodiment 1
[0052] Example 1: MPEG2000 5.0g was used as an initiator, lactide (DL) 5.0g, lactide 0.2% stannous octoate was catalyzed by melt polymerization at 125°C, and the reaction time was 24h. The reaction vessel was repeatedly evacuated 3 times, and nitrogen was protected during the reaction. After the reaction, the product was dissolved with an appropriate amount of tetrahydrofuran, precipitated in glacial ether, and the white precipitate was vacuum-dried for 24 hours.
Embodiment 2
[0053] Example 2: MPEG2000 5.0g was used as an initiator, lactide (DL) 4.0g, lactide 0.2% stannous octoate was catalyzed by melt polymerization at 125°C, and the reaction time was 24h. The reaction vessel was repeatedly evacuated 3 times, and nitrogen was protected during the reaction. After the reaction, the product was dissolved with an appropriate amount of tetrahydrofuran, precipitated in glacial ether, and the white precipitate was vacuum-dried for 24 hours.
Embodiment 3
[0054] Example 3: MPEG2000 5.0g was used as an initiator, lactide (DL) 2.5g, lactide 0.2% stannous octoate catalyzed melt polymerization at 125°C, and the reaction time was 24h. The reaction vessel was repeatedly evacuated 3 times, and nitrogen was protected during the reaction. After the reaction, the product was dissolved with an appropriate amount of tetrahydrofuran, precipitated in glacial ether, and the white precipitate was vacuum-dried for 24 hours.
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