Coating simultaneously having responsive medicine releasing and antibacterial functions, and preparation method of same
A responsive and coating technology, applied in the field of antibacterial surfaces and antibacterial coatings, can solve the problems of uncontrollable drug release and bacterial resistance, and achieve controllable coating preparation process, high drug loading efficiency, and simple equipment. Effect
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Embodiment 1
[0024] (1) Preparation of redox responsive random copolymer: Weigh 0.288g PDSA, 0.406g DMAC 12 and 0.0059g of 2,2-azobisisobutyrocyanide were added to the round bottom flask successively, and 15mL of N,N-dimethylformamide was added as a solvent, nitrogen gas was passed for 30min, and the reaction was carried out at 70°C for 20h. Redox-responsive random copolymers can be obtained by repeated precipitation three times in anhydrous ether and vacuum drying;
[0025] (2) Preparation of drug-loaded colloidal particles: Dissolve the random copolymer prepared in step (1) and the small molecule drug example paracetamol in N,N-dimethylformamide to form a 40 mg / mL solution, and the paracetamol concentration is 10 mg / mL mL, ultrapure water was added dropwise to the above solution at a volume ratio of 1:1, the random polymer self-assembled, and part of the paracetamol was coated in the random copolymer micelles to form redox-responsive drug-loaded micelles;
[0026] (3) Preparation of a c...
Embodiment 2
[0028] (1) Preparation of redox responsive random copolymer: Weigh 0.48g PDSA, 0.4872g DMAC 12 , 0.08gMMA and 0.0059g 2,2-azobisisobutylcyanide were added to the round-bottomed flask in turn, and 20mL N,N-dimethylformamide was added as a solvent, nitrogen gas was passed for 30min, and the reaction was carried out at 65°C for 24h. The reaction solution was repeatedly precipitated in anhydrous ether three times, and vacuum-dried to obtain a redox-responsive random copolymer;
[0029] (2) Preparation of drug-loaded colloidal particles: Dissolve the random copolymer prepared in step (1) and the small molecule drug example paracetamol in N,N-dimethylformamide to form a 40 mg / mL solution, and the paracetamol concentration is 10 mg / mL mL, ultrapure water was added dropwise to the above solution at a volume ratio of 1:1, the random polymer self-assembled, and part of the paracetamol was coated in the random copolymer micelles to form redox-responsive drug-loaded micelles;
[0030] (3...
Embodiment 3
[0032] (1) Preparation of redox-responsive random copolymer: Weigh 0.48g PDSA, 0.4872g DMAC12, 0.08gMMA and 0.0059g 2,2-azobisisobutyrocyanide, add them to a round bottom flask in turn, add 20mL N,N-dimethylformamide was used as a solvent, nitrogen gas was passed for 30 minutes, and the reaction was carried out at 65°C for 24 hours. The reaction solution was repeatedly precipitated in anhydrous ether three times, and vacuum-dried to obtain a redox-responsive random copolymer;
[0033] (2) Preparation of drug-loaded colloidal particles: Dissolve the random copolymer prepared in step (1) and the small molecule drug example paracetamol in N,N-dimethylformamide to form a 20 mg / mL solution, and the paracetamol concentration is 5 mg / mL mL, ultrapure water was added dropwise to the above solution at a volume ratio of 1:2, the random polymer self-assembled, and part of the paracetamol was coated in the random copolymer micelles to form redox-responsive drug-loaded micelles;
[0034] (3)...
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