Slow-release nano drug carrier as well as preparation method and application thereof
A nano-drug carrier and sustained-release technology, used in drug combinations, pharmaceutical formulations, anti-tumor drugs, etc., can solve problems such as side effects and reduced drug availability, and achieve the effect of improving the sustained-release effect.
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Embodiment 1
[0026] Distill 100mg from P(MEO 2 The nanomicelles formed by MA-co-OEGMA-co-DMAEMA)-b-PLGA) were added to the Tris buffer solution of pH 8.5, and the concentration of Tris after adding was 10mmol / L. Add 50 mg of dopamine, react for 24 hours, and centrifuge at 60,000 rpm to obtain slow-release nano drug carrier.
[0027] Among them, P(MEO 2 The weight average molecular weight of MA-co-OEGMA-co-DMAEMA)-b-PLGA) is 16.4kDa; the structure of micelles is W / O / W; the size of the slow-release nano drug carrier is about 100nm.
Embodiment 2
[0029] Distill 100mg from P(MEO 2 The nanomicelles formed by MA-co-OEGMA-co-DMAEMA)-b-PLGA) were added to the Tris buffer solution of pH 7.5, and the concentration of Tris after adding was 1 mmol / L. Then add 10 mg of dopamine, react for 4 hours, and centrifuge at 10,000 rpm to obtain slow-release nano drug carrier.
[0030] Among them, P(MEO 2 The weight-average molecular weight of MA-co-OEGMA-co-DMAEMA)-b-PLGA) is 16.4kDa; the size of the slow-release nano drug carrier is about 100nm.
Embodiment 3
[0032] Distill 10mg from P(MEO 2 The nanomicelles formed by MA-co-OEGMA-co-DMAEMA)-b-PLGA) were added to the Tris buffer solution of pH 10.5, and the concentration of Tris after adding was 20mmol / L. Add 100 mg of dopamine, react for 48 hours, and centrifuge at 100,000 rpm to obtain sustained-release nano drug carrier.
[0033] Among them, P(MEO 2 The weight-average molecular weight of MA-co-OEGMA-co-DMAEMA)-b-PLGA) is 16.4kDa; the size of the slow-release nano drug carrier is about 100nm.
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