Anti-cancer drug nanocapsule with near-infrared photothermal response and preparation method thereof
An anti-cancer drug and near-infrared light technology, which is applied in the direction of drug combination, microcapsules, and capsule delivery, can solve problems such as no longer having near-infrared photothermal effect, failure of photothermal nano drug capsules, and stability of gold nanorods. , to achieve long-term stable photothermal conversion efficiency, ultra-high photothermal conversion efficiency, and high drug loading effect
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Embodiment 1
[0019] a.0.5mgCu 1.75 S nanosheets were dispersed in 5.0mL chloroform, 8uL allyl mercaptan (Alm) was added and stirred slowly at 30°C for 30 minutes; after that, acetone was added to the solution, centrifuged (10000r / min, 10min), and then chloroform and acetone The excess Alm was washed away, and this purification process was repeated 3 times to obtain Cu 1.75 S allyl thiol nanoparticles were then dispersed into 1.0 mL of chloroform;
[0020] b. 1.0mL contains 0.5mg of Cu 1.75 A chloroform dispersion of S allylthiol nanoparticles was mixed with 15 mL containing 300 mg N-isopropylacrylamide (NIPAM, monomer), 15 μg methacrylic acid (MAA, monomer) and 5 mg bisacrylamide (MBA, cross-linking agent). ) of sodium dodecylsulfonate (SDS) solution (sodium dodecylsulfonate concentration 1.0mg / mL), under vigorous stirring and ultrasound, a brown emulsion was obtained; chloroform was evaporated at 58°C for 20 minutes; then heated to 70°C, quickly add 1.0mL (10mg / mL) potassium persulfate...
Embodiment 2
[0024] a.0.5mgCu 1.75 S nanosheets were dispersed in 5.0mL chloroform, 8uL allyl mercaptan (Alm) was added and stirred slowly at 30°C for 30 minutes; after that, acetone was added to the solution, centrifuged (10000r / min, 10min), and then chloroform and acetone The excess Alm was washed away, and this purification process was repeated 3 times to obtain Cu 1.75 S allyl thiol nanoparticles were then dispersed into 1.0 mL of chloroform;
[0025] b. 1.0mL contains 0.5mg of Cu 1.75 Chloroform dispersion of S allylthiol nanoparticles was mixed with 15 mL containing 300 mg N-isopropylacrylamide (NIPAM, monomer), 15 μg methacrylic acid (MAA, monomer) and 10 mg bisacrylamide (MBA, crosslinker ) in sodium dodecylsulfonate (SDS) solution (1.0mg / mL), under vigorous stirring and ultrasonication, a brown emulsion was obtained; chloroform was evaporated at 58°C for 20 minutes; then heated to 70°C, and 1.0mL ( 10mg / mL) potassium persulfate (KPS, initiator) solution, maintain at 70°C for 5 ...
Embodiment 3
[0028] a.0.5mgCu 1.75 S nanosheets were dispersed in 5.0mL chloroform, 8uL allyl mercaptan (Alm) was added and stirred slowly at 30°C for 30 minutes; after that, acetone was added to the solution, centrifuged (10000r / min, 10min), and then chloroform and acetone The excess Alm was washed away, and this purification process was repeated 3 times to obtain Cu1.75 S allyl thiol nanoparticles were then dispersed into 1.0 mL of chloroform;
[0029] b. 1.0mL contains 0.5mg of Cu 1.75 Chloroform dispersion of S allylthiol nanoparticles was mixed with 15 mL containing 300 mg N-isopropylacrylamide (NIPAM, monomer), 15 μg methacrylic acid (MAA, monomer) and 15 mg bisacrylamide (MBA, crosslinker ) in sodium dodecylsulfonate (SDS) solution (1.0mg / mL), under vigorous stirring and ultrasonication, a brown emulsion was obtained; chloroform was evaporated at 58°C for 20 minutes; then heated to 70°C, and 1.0mL ( 10mg / mL) potassium persulfate (KPS, initiator) solution, maintain at 70°C for 5 ho...
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