Preparation method of allyl isothiocyanate nanometer lipid carrier
A technology of nano-lipid carrier and isothiocyanate, which is applied in the directions of non-active ingredients such as medical preparations, pharmaceutical formulations, ester active ingredients, etc. Limit the application and other problems to achieve the effect of prolonging the local aggregation, high drug loading, and clear targeting
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[0034] When the allyl isothiocyanate nano lipid carrier of the present invention is prepared, its preparation method comprises the following steps:
[0035] (1) Dissolve allyl isothiocyanate, solid lipid material, liquid oil, and fat-soluble emulsifier in an organic solvent, then remove the organic solvent by vacuum rotary evaporation or vacuum drying, and heat to 60~ Melting at 100°C to form the organic phase;
[0036] (2) Dissolve long-circulation excipients, water-soluble emulsifiers, and additives in water for injection, and heat to 60-100°C to form the water phase;
[0037] (3) mixing the organic phase and the aqueous phase under stirring or high shear conditions at a temperature of 60-100° C. to prepare colostrum;
[0038] (4) Ultrasonic or high-pressure homogenization is performed on the colostrum to prepare the allyl isothiocyanate nano-lipid carrier.
[0039] The obtained allyl isothiocyanate nano-lipid carrier can be further lyophilized or kept sealed at 4°C, where...
Embodiment 1
[0041] An allyl isothiocyanate nano lipid carrier, which is composed of: allyl isothiocyanate 5mg, GMS60mg, MCT20uL, lecithin 150mg, absolute ethanol 5mL, PEG200020mg, Tween8040mg, water for injection 50mL.
[0042] The preparation method is as follows:
[0043] Dissolve allyl isothiocyanate, GMS, MCT, and lecithin in absolute ethanol, remove the absolute ethanol by rotary evaporation under reduced pressure, and heat to 80°C to melt to form an organic phase; dissolve PEG2000 and Tween80 in water for injection and heated to 80°C to form the water phase; at a temperature of 80°C, the organic phase and the water phase were mixed under stirring conditions to prepare colostrum; the colostrum was subjected to high-pressure homogenization , and poured into ice water to prepare allyl isothiocyanate nano lipid carrier.
[0044] The drug loading and encapsulation efficiency of allyl isothiocyanate nano-lipid carriers were determined to be 7.82% and 87.6% respectively
Embodiment 2
[0046] A nano-lipid carrier of allyl isothiocyanate, which is composed of: 5 mg of allyl isothiocyanate, 60 mg of GMS, 20 uL of MCT, 150 mg of lecithin, 5 mL of absolute ethanol, 20 mg of PEG2000, 40 mg of Tween8040 mg, and 100 mL of water for injection.
[0047] The preparation method is as follows:
[0048] Dissolve allyl isothiocyanate, GMS, MCT, and lecithin in absolute ethanol, remove the absolute ethanol by rotary evaporation under reduced pressure, and heat to 80°C to melt to form an organic phase; dissolve PEG2000 and Tween80 in water for injection and heated to 80°C to form an aqueous phase; at a temperature of 80°C, the organic phase and the aqueous phase were mixed under stirring conditions to prepare colostrum; the colostrum was subjected to high-pressure homogenization , and poured into ice water to prepare allyl isothiocyanate nano lipid carrier.
[0049] The drug loading and encapsulation efficiency of allyl isothiocyanate nanolipid carriers were determined to ...
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