Anti-tumor nano preparation and application thereof in targeted therapy of malignant tumors
A nano-preparation and targeted therapy technology, applied in the field of anti-tumor nano-preparation and its application in targeted therapy of malignant tumors, can solve the problems such as not many, can not achieve the optimal effect, achieve small trauma area, non-toxic Side effects, effect of high photothermal conversion efficiency
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Embodiment 1
[0046] The preparation steps of polydopamine nanoparticles and polydopamine nanoparticle core-loaded epidoxorubicin nano preparations are as follows:
[0047] S1: Take 1g of L-cysteine and 6ml of 25% ammonia water and add them to 260ml of 30% ethanol solution, stir and mix evenly, and then add 0.26 mol / 1 dopamine hydrochloride to the mixed solution in a water bath at 35℃ for 10 min. m1, continue to stir and react for 24 hours to obtain PDA-NPS;
[0048] S2: After dialysis in the PDA-NPS dialysis tube obtained in step S1, continue to dilute it by 2 times with water to obtain solution A;
[0049] S3: Add the excipient drug loading agent, water-based binder, and epirubicin (EPI) in a mass ratio of 12:4:1 into 2 ml methanol to fully dissolve them to obtain solution B;
[0050] S4: Take the solution B of step S3 and slowly drop it into the solution A of step S2. Shake while dripping. After mixing well, place the mixture in a 37 ℃ water bath for 30 min; at the end of the water bath, dialy...
Embodiment 2
[0053] The preparation steps of polydopamine nanoparticles and polydopamine nanoparticle core-loaded epidoxorubicin nano preparations are as follows:
[0054] S1: Take 1 g of L-cysteine and 6 ml of 25% ammonia water and add them to 260 ml of 30% ethanol solution, stir and mix evenly, bathe in a dark water bath at 0°C for 5 minutes, and add 0.26 mol / l dopamine hydrochloride to the mixed solution 60 ml, continue to stir and react for 72 h to obtain PDA-NPS;
[0055] S2: After dialysis in the PDA-NPS dialysis tube obtained in step S1, continue to dilute it with water 6 times to obtain solution A;
[0056] S3: Add the excipient drug loading agent, water-based binder, and epirubicin (EPI) in a mass ratio of 6:10:1 into 2 ml of methanol to fully dissolve them to obtain solution B;
[0057] S4: Take the solution B of step S3 and slowly drop it into the solution A of step S2, shake while dripping, and place the mixture in a 45 ℃ water bath for 25 min after mixing thoroughly; at the end of t...
Embodiment 3
[0060] The preparation steps of polydopamine nanoparticles and polydopamine nanoparticle core-loaded epidoxorubicin nano preparations are as follows:
[0061] S1: Take 1 g of L-cysteine and 6 ml of 25% ammonia water and add them to 260 ml of 30% ethanol solution, stir and mix well, bath in a dark water bath at 40°C for 7 minutes, and add 0.26 mol / l dopamine hydrochloride to the mixed solution 80 ml, continue to stir and react for 0.5 h to obtain PDA-NPS;
[0062] S2: After dialysis in the PDA-NPS dialysis tube obtained in step S1, continue to dilute it with water 8 times to obtain solution A;
[0063] S3: Add the excipient drug loading agent, aqueous binder, and epirubicin (EPI) in a mass ratio of 1:2:1 into 2 ml of methanol to fully dissolve them to obtain solution B;
[0064] S4: Take the solution B of step S3 and slowly drop it into the solution A of step S2. Shake while dripping. After mixing thoroughly, place the mixture in a 30 ℃ water bath for 30 min; at the end of the water ...
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