Drug carrier of apigenin and preparation method
A kind of technology of apigenin and medicine, applied in the field of drug carrier and preparation of apigenin, can solve the problems of high phase transition temperature and unfavorable application of sucrose ester, achieve high antioxidant activity, increase antioxidant activity, and increase solubility
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[0043] Phase Diagram Preparation
[0044] First, a certain mass ratio of surfactant S1570 / NaDC is placed in a stoppered colorimetric tube, and isopropanol is added in a mass ratio of 6:4 between surfactant and co-surfactant isopropanol to form a mixed Surfactant system (EM). Secondly, according to the mass ratio of the mixed surfactant and oil from 10:0 to 0:10, the oil phase was weighed successively in different colorimetric tubes, and stirred and mixed with a vortex mixer. Mix well, then stir and dissolve at 50-60°C. Add double-distilled water dropwise to the colorimetric tube at intervals of 2%, and finally observe it in a constant temperature water bath at 40°C, and determine the microemulsion phase region by the clear, transparent and flowable appearance.
[0045] The phase behavior of the S1570 / NaDC / isopropanol / isoamyl acetate / 5% NaCl aqueous solution system was studied at 40°C by introducing different contents of NaDC. The pseudo-ternary phase diagram is shown in figu...
Embodiment 1
[0055] Place 2.295g sucrose stearate, 0.405g sodium deoxycholate, 1.8g isopropanol and 0.5g isoamyl acetate in a stoppered colorimetric tube, mix it evenly with a vortex mixer, and set it at 50- Fully stir in a constant temperature water bath at 60°C to dissolve it. Then, 5g of 5% NaCl aqueous solution was added dropwise to the colorimetric tube, placed in a water bath, stirred and mixed, and finally left to stand in a constant temperature water bath at 40°C to achieve phase equilibrium, and the obtained microemulsion was the drug-loaded microemulsion. Emulsion, denoted as P 1 .
Embodiment 2
[0057] Place 2.16g sucrose stearate, 0.54g sodium deoxycholate, 1.8g isopropanol and 0.5g isoamyl acetate in a stoppered colorimetric tube, mix it evenly with a vortex mixer, and set it at 50- Fully stir in a constant temperature water bath at 60°C to dissolve it. Then, 5g of 5% NaCl aqueous solution was added dropwise to the colorimetric tube, placed in a water bath, stirred and mixed, and finally left to stand in a constant temperature water bath at 40°C to achieve phase equilibrium, and the obtained microemulsion was the drug-loaded microemulsion. Emulsion, denoted as P 2 .
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