Preparation method of invisible thermosensitive liposome as well as application of drug delivery system of invisible thermosensitive liposome in tumor treatment drugs
An invisible heat-sensitive lipid and heat-sensitive liposome technology, which can be used in anti-tumor drugs, liposome delivery, drug combination and other directions, can solve problems such as large side effects and poor treatment effects, and achieve low side effects and preparation conditions. Simple and feasible, the effect of rich source of raw materials
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Embodiment 1
[0020] The preparation method of the present invention can be realized by the following steps in concrete implementation:
[0021] (1) Synthesis of carboxylated carbon nanotubes: Weigh 100mg of carbon nanotubes, put them into a 250mL round bottom flask, add 120mL of mixed acid, 12mL of hydrogen peroxide solution with a mass concentration of 30%, and put them in an ultrasonic cleaner for 1 hour. Add 1L of ultrapure water to dilute, filter with 0.22 μm microporous membrane and Buchner funnel, rinse with ultrapure water until the pH is neutral, put it in an oven and dry at a constant temperature of 80°C to obtain carboxylated carbon nanotubes (CNTs- COOH); the mixed acid is a mixed acid composed of concentrated sulfuric acid and concentrated nitric acid in a volume ratio of 3:1;
[0022] (2) Synthesis of folic acid-targeted carbon nanotubes-lysine: Weigh 50 mg of carboxylated carbon nanotubes, add 25 mL of 0.2 M lysine solution, then add 10 mg of folic acid, 50 mg of 1-ethyl-(3- ...
Embodiment 2
[0025] The preparation method of the present invention can also be realized by the following steps in specific implementation:
[0026](1) Synthesis of carboxylated carbon nanotubes: Weigh 105 mg of carbon nanotubes, put them into a 250 mL round bottom flask, add 120 mL of mixed acid, 13 mL of hydrogen peroxide solution with a mass concentration of 30%, and sonicate in an ultrasonic cleaner for 1 hour. Add 1L of ultrapure water to dilute, filter with 0.22 μm microporous membrane and Buchner funnel, rinse with ultrapure water until the pH is neutral, put it in an oven and dry at a constant temperature of 80°C to obtain carboxylated carbon nanotubes (CNTs- COOH);
[0027] (2) Synthesis of folic acid-targeted carbon nanotubes-lysine: Weigh 53 mg of carboxylated carbon nanotubes, add 25 mL of 0.2 M lysine solution, then add 11 mg of folic acid, 53 mg of 1-ethyl-(3- Dimethylaminopropyl) carbodiimide hydrochloride (EDC·HCl), 11mg N-hydroxysuccinimide (NHS), placed in a flask, after...
Embodiment 3
[0030] The preparation method of the present invention can be realized by the following steps in concrete implementation:
[0031] (1) Synthesis of carboxylated carbon nanotubes: Weigh 100mg of carbon nanotubes, put them into a 250mL round bottom flask, add 120mL of mixed acid, 12mL of hydrogen peroxide solution with a mass concentration of 30%, and after ultrasonic cleaning for 1h, add Dilute with 1L of ultrapure water, filter with 0.22μm microporous membrane and Buchner funnel, rinse with ultrapure water until the pH is neutral, and dry in an oven at 80°C to obtain carboxylated carbon nanotubes (CNTs-COOH) ;
[0032] (2) Synthesis of carbon nanotubes loaded with doxorubicin hydrochloride-lysine: Weigh 50 mg of carboxylated carbon nanotubes, add 25 mL of 0.2M lysine solution, 50 mg of 1-ethyl-(3-dimethylaminopropyl base) carbodiimide hydrochloride (EDC·HCl) and 10 mg N-hydroxysuccinimide (NHS), placed in a flask, ultrasonically dispersed for 2 hours, then stirred at 100 r / mi...
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