Nano Chinese medicine threewingnut/Tripterygium prepn and its prepn process
A technology of nano-Chinese medicine and Tripterygium wilfordii, which is applied in the direction of nano-structure manufacturing, nano-technology, and pharmaceutical formulations, and can solve problems such as high toxicity
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Embodiment 1
[0064] Embodiment 1: 1. Preparation of blank solid lipid nanoparticles:
[0065] Take 200mg of stearic acid and 100mg of soybean lecithin, dissolve in 10ml of cyclohexane to form an organic phase; take another 0.75g of polyethylene glycol monostearate, stir and dissolve in 35ml of water to form an aqueous phase. The aqueous phase was heated to 70°C. While stirring rapidly, inject the organic phase into the water phase with a No. 6 needle, and continue stirring to completely evaporate the organic solvent and concentrate the system to 15 ml. Add 35ml of distilled water at 0-2°C, then sonicate for 10min, and dilute to 50ml to obtain a light blue transparent colloidal solution. The average particle size is 106 nm, and the polydispersity index is 0.228.
[0066] The preparation of blank solid lipid nanoparticles is mainly to provide reference samples for subsequent drug efficacy experiments and toxicity experiments. 2. Preparation of tripterygium wilfordii solid liposome nanopar...
Embodiment 2
[0072] Take Tripterygium wilfordii extract 200mg, soybean lecithin 100mg, dissolve in 5ml of ethanol, take another 200mg of triolein, dissolve in 5ml of cyclohexane, mix and stir evenly. Remove the organic solvent by rotary evaporation under reduced pressure in a constant temperature water bath at 45°C, so that the drug and excipients form a uniform lipid film on the wall of the flask, and then place it in a vacuum desiccator overnight to remove the organic solvent; another polyoxyethylene / polyoxyethylene 750 mg of propylene copolymer was stirred and dissolved in 35 ml of water, added to the above film, then ultrasonically treated for 15 min, and the volume was adjusted to 50 ml to obtain a dark yellow transparent colloidal solution.
Embodiment 3
[0074] Take tripterygium wilfordii extract 200mg, soybean lecithin 100mg, dissolve in 5ml of ethanol, take another 250mg of glycerol monooleate, dissolve in 5ml of cyclohexane, mix and stir evenly. Remove the organic solvent by rotary evaporation under reduced pressure in a constant temperature water bath at 45°C, so that the drug and excipients form a uniform lipid film on the wall of the flask, and then place it in a vacuum desiccator overnight to remove the organic solvent; another polyoxyethylene / polyoxyethylene 800mg of propylene copolymer was stirred and dissolved in 35ml of water, added to the above film, then ultrasonically treated for 15min, and the volume was adjusted to 50ml to obtain a dark yellow transparent colloidal solution.
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