Anti-tumor magnetic drug-loading hybridized nanocapsules and preparation method thereof
A nanocapsule, anti-tumor technology, applied in the field of biomedical materials, can solve the problems of poor biocompatibility, drug release can not be well controlled, etc., to achieve good anti-tumor, good photothermal response behavior, inhibition of multiple The effect of drug resistance
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Embodiment 1
[0065] Example 1 Fe 3 o 4 Preparation of -OA
[0066] in N 2 Under protective conditions, add Fe(acac) to the three-necked bottle 3 , 1,2-hexadecanediol, OA and oleylamine, and finally add dibenzyl ether. Use a sand bath to heat, wait until the temperature rises slowly to 200°C, keep it warm for 2 hours, then slowly raise the temperature to 265°C, hold it for 1 hour, then cool to room temperature. The reactant in the three-neck flask was transferred to the Erlenmeyer flask for magnetic separation. After the magnetic separation was completed, the supernatant was poured off, and a small amount of ethanol was added to transfer the black precipitate to a centrifuge tube for centrifugation (3000 r / min, 5 min). The supernatant obtained by centrifugation was discarded, a small amount of n-hexane was added dropwise, and the black precipitate was transferred to a high-speed centrifuge tube for centrifugation (8000r / min, 10min). Pipette the upper layer suspension into a conical fl...
Embodiment 2
[0067] Example 2 TPGS-Cystamine-NH 2 and HO-PEG-Cystamine-NH 2 preparation of
[0068] Weigh TPGS, succinic anhydride and DMAP in a round-bottomed flask, dissolve with anhydrous dichloromethane, and place in N 2 The reaction was carried out under anhydrous and oxygen-free conditions for 24 hours. After the reaction was completed, the reaction solution was filtered, and the filtrate was collected. In a dialysis bag (cut-off Mw=1KDa), dialyze with 50% ethanol for 48h, then dialyze in deionized water for 48h, and freeze-dry to obtain the product, named TPGS-COOH; wherein TPGS, succinic anhydride and DMAP The mass ratio is 7.69:1:1.31.
[0069] The TPGS-COOH obtained above, EDC·HCl, NHS and cystamine hydrochloride were dissolved in deionized water in a round bottom flask, and the pH was adjusted to 6-7, and then reacted for 48 hours under magnetic stirring. After the reaction was completed, it was dialyzed in deionized water for three days (cut-off Mw=1KDa), and freeze-dried ...
Embodiment 3
[0072] Example 3 Preparation of Hep-TPGS-PEG-COOH
[0073] Sodium heparin, TPGS-Cystamine-NH 2 and HO-PEG-Cystamine-NH 2 Put it into a round bottom flask, then add EDC·HCl and NHS, mix well, then dissolve with deionized water, and adjust the pH of the solution to 6-7. After 48 hours of magnetic stirring reaction, the liquid was transferred to a dialysis bag (cut-off Mw=3500Da) and dialyzed with deionized water for 72 hours, and finally freeze-dried to obtain Hep-TPGS-PEG-OH. Among them, heparin sodium, TPGS-Cystamine-NH 2 , HO-PEG-Cystamine-NH 2 The mass ratio of , EDC·HCl and NHS is 4:1:1:2.24:1.36.
[0074] Put the Hep-TPGS-PEG-OH prepared above, succinic anhydride and DMAP in a round-bottomed branch bottle, dissolve with anhydrous DMF, react at room temperature under nitrogen protection for 24 hours, dialyze and freeze-dry to obtain PEG on the branched chain The heparin graft modification Hep-TPGS-PEG-COOH with -COOH at the end, wherein the mass ratio of Hep-TPGS-PEG-O...
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