Curcumin colon-targeted medicine preparation and preparation method thereof
A colon-targeting and pharmaceutical preparation technology, which is applied in drug combination, drug delivery, pharmaceutical formulation, etc., can solve the problems of low drug stability, incomplete drug release, and small drug loading, so as to reduce the volume of the preparation and effectively Facilitate dissolution and absorption, improve solubility and stability
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Embodiment 1
[0047] Embodiment 1 curcumin-beta-cyclodextrin inclusion compound preparation
[0048] Get 300g beta-cyclodextrin and be dissolved in the aqueous ethanol solution of 1000g (mass percentage concentration is 50%); Place in constant temperature magnetic stirrer, keep temperature 40 ℃, add the dehydrated alcohol solution that 600g contains curcumin (curcumin 100g, without 500 g of water and ethanol), stirring while adding, and after 2 hours of inclusion, put the suspension containing the inclusion compound in the refrigerator for 24 hours, then suction filter, wash the solid with absolute ethanol, and reduce the inclusion compound at 40 ° C. Press and dry to obtain yellow curcumin-β-cyclodextrin inclusion compound powder.
Embodiment 2
[0049] The preparation of embodiment 2 curcumin-hydroxypropyl β-cyclodextrin inclusion compound
[0050] Dissolve 300g of hydroxypropyl β-cyclodextrin in 1000mL of water, place it in a constant temperature magnetic stirrer, add 1100g of curcumin-containing acetone solution (100g of curcumin, 1000g of acetone) while stirring at 40°C, stir for 2h, and use Filter through a 0.45 μm microporous membrane, and spray-dry the filtrate to obtain a yellow loose powder of curcumin-hydroxypropyl β-cyclodextrin inclusion compound.
Embodiment 3
[0051] The preparation of embodiment 3 curcumin-alpha-cyclodextrin inclusion compound
[0052] Dissolve 200g of α-cyclodextrin in 1500mL of water, place it in a constant temperature magnetic stirrer, add 900g of curcumin-containing propylene glycol solution (100g of curcumin, 800g of propylene glycol) while stirring at 40°C, stir for 2h, and use 0.45μm Filter through a microporous membrane, and freeze-dry the filtrate for 24 hours to obtain curcumin-α-cyclodextrin inclusion complex yellow loose freeze-dried powder.
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