Micro-embedded medicament carrier and preparation method thereof
A nano-carrier and drug technology, which is applied in the field of micro-encapsulated drug carrier and its preparation, can solve the problems of insufficient protection of drug activity, single means of adjusting drug dissolution rate, drug cross-contamination, etc., to solve cross-interference and commonly used micro/nano The effect of carrier burst release, inhibition of burst release effect, and reduction of toxic and side effects
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Embodiment 1
[0020] A microencapsulated drug carrier, which forms a microencapsulated drug carrier by embedding nanocarriers inside the microcapsules, and the drugs are respectively carried inside the nanoparticles or between different nanoparticles in the microcapsules. The particle size of the nano-carrier is between 100-1000nm, and the particle size of the micro-encapsulation system is between 100-1000μm.
[0021] A preparation method of a microencapsulated drug carrier according to the present embodiment comprises the following preparation steps: (1) using an aqueous sodium alginate solution with a concentration of 1.0% (w / v), passing through micropores of 0.8 μm, 0.45 μm, and 0.22 μm Membrane filtration is used as the water phase, and the isooctane solution of Span 80 with a concentration of 4.0% (w / v) is the oil phase. Mix the same volume of the water phase and the oil phase, and use a stirrer at 1500 rpm to fully stir and mix to form an emulsified After the W / O system, add 2 mL of T...
Embodiment 2
[0025] This embodiment is basically the same as Embodiment 1, except that the sodium alginate solution in the syringe pump is mixed with 1 mg / mL fluorouracil. A microencapsulation system for distributing different drugs in different internal spaces was prepared, that is, BSA was embedded inside the nanocapsule, and fluorouracil was embedded in the microcapsule outside the nanocapsule. The drug loadings of BSA and fluorouracil in the microencapsulation system were 7.07% and 0.23%, respectively, and the encapsulation efficiencies were 63.78% and 29.32%, respectively. The cumulative release of fluorouracil was more than 80% in the simulated release in vitro of the microencapsulation system until the 7th day, while that of BSA was only about 10%. The new microencapsulated drug carrier of this embodiment further improves the long-term release and absorption of the drug after being mixed with fluorouracil in the sodium alginate solution, and reduces the toxic and side effects of the...
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