A kind of docetaxel nanoparticle composition
A technology of docetaxel and composition, which is applied in the direction of drug combination, drug delivery, organic active ingredients, etc. It can solve the problems of low negative phospholipid content, high price, and health hazards for patients with cardiovascular and cerebrovascular diseases, and achieve high encapsulation efficiency , low price, and the effect of improving drug safety
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Embodiment 1
[0036]Prescription: Docetaxel 1g
[0037] Hydrogenated Soy Lecithin 70g
[0038] 0.01NpH6.5 phosphate buffer (sodium dihydrogen phosphate or??, should be specific) 870ml
[0039] Preparation Process:
[0040] 1. Dissolve the prescription amount of docetaxel and hydrogenated soybean lecithin in 80ml of ethanol as the organic phase;
[0041] 2. Take 870ml of 0.01N pH6.5 phosphate buffer, heat it to 65°C and use it as the water phase;
[0042] 3. Slowly inject the organic phase into the water phase under nitrogen protection and stirring, and stir thoroughly for 30 minutes to obtain the nanoparticle suspension;
[0043] 4. Pass the nanoparticle suspension into a high-pressure homogenizer to homogenize for 5 times, then sterilize and filter, and pack aseptically.
Embodiment 2
[0045] Prescription: Docetaxel 1g
[0047] Sucrose 60g
[0048] Preparation Process:
[0049] 1. Dissolve the prescription amount of docetaxel and egg yolk lecithin in 22ml of ethanol as the organic phase;
[0050] 2. Take the prescribed amount of sucrose, add 230ml of water for injection to dissolve it as the water phase;
[0051] 3. Heat the water phase to 40°C at a constant temperature, slowly inject the organic phase into it under nitrogen protection and stirring, and shear for 30 minutes to obtain the nanoparticle suspension;
[0052] 4. Pass the nanoparticle suspension into a high-pressure homogenizer for homogenization 5 times, sterilize and filter, divide into vials for freeze-drying, and pack.
Embodiment 3
[0054] Prescription: Docetaxel 1g
[0055] Hydrogenated Soy Lecithin 25g
[0056] Soy Lecithin 15g
[0057] Maltose 45g
[0058] Preparation Process:
[0059] 1. Dissolve the prescription amount of docetaxel, hydrogenated soybean lecithin and soybean lecithin in 35ml ethanol as the organic phase;
[0060] 2. Take the prescribed amount of maltose, add 450ml of water for injection to dissolve it as the water phase;
[0061] 3. Heat the water phase to 70°C at a constant temperature, slowly inject the organic phase into it under nitrogen protection and stirring, and then shear for 20 minutes to obtain the nanoparticle suspension;
[0062] 4. Pass the nanoparticle suspension into the extruder and extrude it for 6 times, then sterilize and filter, put it into vials for freeze-drying, and pack.
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