Microencapsulated multivesicular liposome drug carrier and preparation method thereof
A multivesicular liposome and microcapsule technology, applied in microcapsules, capsule delivery, pharmaceutical formulations, etc., can solve the problems of general biocompatibility, differences in physical and chemical properties, cross-contamination of drugs, etc., and achieve smooth surface of microcapsules, Easy to operate and reduce toxic and side effects
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[0022] The present invention also relates to a preparation method of the above-mentioned microcapsule-embedded polyvesicular liposome drug carrier, the steps of the preparation method are as follows:
[0023] Step 10, using sucrose solution as the inner water phase, glucose and L-lysine solution as the outer water phase, and lipid-dissolved dichloromethane solution as the oil phase, high-speed homogenizing and emulsifying the inner water phase and the oil phase to form an initial phase After milking, add the external water phase, vortex emulsify to form a double emulsion, and then rotate to evaporate the dichloromethane to obtain the multivesicular liposome suspension;
[0024] Step 20, take quantitative multivesicular liposomes and disperse them in the sodium alginate solution, disperse evenly with the aid of ultrasonic waves, and then drop the sodium alginate solution dispersed in multivesicular liposomes into the chlorine Calcium alginate beads embedded with multivesicular ...
Embodiment 1
[0030] Example 1: prepare 7.5% (w / v) sucrose solution as the inner aqueous phase; prepare a solution containing 5% (w / v) glucose and 30mM L-lysine as the outer aqueous phase; prepare a solution containing 16.5mg / mL Soybean lecithin, 8mg / mL cholesterol, 8mg / mL triolein and 1mg / mL oleic acid in dichloromethane are used as the oil phase; mix the same volume of the internal water phase and oil phase, and stir on a high-speed homogenizer for 10min , with a rotating speed of 14,000 rpm, to prepare colostrum; add 9 mL of external aqueous phase solution to the colostrum, emulsify on a vortex suspension apparatus for 10 seconds, and prepare double milk. Subsequently, the double emulsion was transferred to a rotary evaporator, and the organic solvent was removed by rotary evaporation at 35° C. and 10 rpm. After centrifugation at 3500 rpm for 5 minutes, the multivesicular liposome suspension was obtained. The microsphere has a smooth surface, good dispersibility, good sphericity, an aver...
Embodiment 2
[0032] Embodiment 2: This embodiment is basically the same as Embodiment 1, except that the sodium alginate solution in the syringe pump is mixed with 2 mg / mL insulin solution. A microcapsule-embedded multivesicular liposome drug carrier system that distributes different drugs in different spaces is prepared, that is, MET is embedded inside the multivesicular liposome, and insulin is embedded outside the multivesicular liposome and inside the microcapsule. The drug loading capacity of MET and insulin in the multivesicular liposome drug carrier system embedded in microcapsules was 0.39% and 1.91%, respectively, and the encapsulation efficiency was 57.10% and 11.41%, respectively. The cumulative release of MET was 18.97% and 0% of insulin when the system was simulated in vitro for 4 hours; the cumulative release of MET and INS was close to 22% at 8 hours. It shows a sequential release phenomenon within a certain period of time.
[0033]The invention adopts the double emulsifica...
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