Biological responsiveness targeted double-drug slow-release carrier material and preparation method thereof
A slow-release carrier and responsive technology, which can be used in drug delivery, pharmaceutical formulations, medical preparations with inactive ingredients, etc. It can solve problems such as normal cell damage, toxic side effects, and lower drug utilization efficiency, and achieve good biological responsiveness. , the effect of easy degradation
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Embodiment 1
[0039] A method for preparing a bioresponsive targeted dual-drug slow-release carrier material, comprising the following steps:
[0040](1) Synthesis of RAFT reagents:
[0041] a. Dissolve 2.5g KOH in 2.5mL H 2 Obtain KOH solution in O; Dissolve 10.1g dodecanethiol and 0.64g tetrabutylammonium bromide in 25mL acetone, then mix it with KOH solution;
[0042] b. Slowly add 2.6mL of carbon disulfide to the mixed solution obtained in step (a) dropwise, stir for 30 minutes, add 5mL of chloroform to it, and stir for another 10min; place the solution at 0°C, and add dropwise while stirring KOH solution (12.0g KOH dissolved in 10mL H 2 O), after the dropwise addition was completed, it was placed at room temperature and stirred overnight;
[0043] c. Add 60 mL of deionized water to the solution obtained in step (b), then add 10 mL of concentrated hydrochloric acid for acidification; the resulting product is vacuum-dried to obtain a solid product; recrystallized with isopropanol, and...
Embodiment 2
[0055] A method for preparing a bioresponsive targeted dual-drug slow-release carrier material, comprising the following steps:
[0056] (1) Synthesis of RAFT reagent: same as Example 1;
[0057] (2) Synthesis of PDSEMA:
[0058] (3) Preparation of amphiphilic single-chain polymer: Dissolve 90mg of RAFT reagent, 7g of PDSEMA, 4g of polyethylene glycol methacrylate (Mw 500) and 10mg of AIBN in 10mL of DMF, and use the freeze-thaw pump circulation method to purify and remove Gas more than 3 times; then seal the reaction mixture, put it into a preheated 70 ℃ oil bath for 12h; 5mL of dichloromethane, and then re-precipitated in 20mL of ether to obtain unreduced amphiphilic polymer single chain;
[0059] (4) Preparation of amphiphilic polymer nanospheres: Dissolve 10 mg of amphiphilic polymer single chain in 200 μL of acetone, slowly add DTT dropwise therein; stir for 10 minutes, add 1 mL of deionized water, and then stir overnight at room temperature , in contact with the air, ...
Embodiment 3
[0063] A method for preparing a bioresponsive targeted dual-drug slow-release carrier material, comprising the following steps:
[0064] (1) Synthesis of RAFT reagent: same as Example 1;
[0065] (2) Synthesis of PDSEMA:
[0066] (3) Preparation of amphiphilic polymer single chain: Dissolve 90mg of RAFT reagent, 5g of PDSEMA, 4g of polyethylene glycol methacrylate (Mw 500) and 10mg of AIBN in 10mL of DMF, and use the freeze-thaw pump circulation method to purify and remove Gas more than 3 times; then seal the reaction mixture, put it into a preheated 70 ℃ oil bath for 12h; 5mL of dichloromethane, and then re-precipitated in 20mL of ether to obtain unreduced amphiphilic polymer single chain;
[0067] (4) Preparation of amphiphilic polymer nanospheres: Dissolve 10 mg of amphiphilic polymer single chain in 200 μL of acetone, slowly add DTT dropwise therein; stir for 10 minutes, add 1 mL of deionized water, and then stir overnight at room temperature , in contact with the air, ...
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