A nanocomposite material with photodynamic and photothermal combined therapy functions and its preparation method and application
A nano-composite material and combined therapy technology, applied in the field of nano-composite materials and its preparation, can solve the problems of limited penetration of photosensitizers, inability to obtain therapeutic effects, power and photothermal recurrence, etc., and achieve high photothermal conversion efficiency, Good photodynamic effect and low cost
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Embodiment 1
[0050] Step 1. Synthesis of metal Ir complexes
[0051]
[0052] Ⅰ) Take 1g of benzothiophene-2-boronic acid, 0.9g of 1-chloroisoquinoline, and 0.3g of tetrakistriphenylphosphine palladium into a 250mL single-necked bottle with a stirrer, blow nitrogen, then add 60mL of toluene, 20mL of ethanol, 20mL of 2M sodium carbonate aqueous solution, reflux and stir overnight, after extraction, spin dry under reduced pressure, after column purification, the white powder is iridium complex Ir-1 compound 1
[0053] Ⅱ) Take 500mg of the product obtained in I and 340mg of iridium chloride trihydrate and add it to a 100mL single-necked bottle with a stirrer, blow nitrogen, then add 30mL of ethylene glycol ether and 10mL of water, reflux and stir for 24 hours, and dry to obtain a brick red color after suction filtration powder compound 2
[0054] Ⅲ) Take 680 mg of the product obtained in step Ⅱ, 130 mg of 3-hydroxy-2-pyridinecarboxylic acid and 300 mg of sodium carbonate in a 100 mL s...
Embodiment 2
[0068] Same as Example 1, the difference lies in Step III and Step 4 in Step 1.
[0069] In step 1, III) take 680 mg of the product obtained in step II, 130 mg of 3-hydroxy-2-pyridinecarboxylic acid and 300 mg of sodium carbonate in a 100 mL single-necked bottle with a stirrer, blow nitrogen, add 30 mL of ethylene glycol ether, and at 100 ° C, Reflux and stir for 24 hours, after extraction, spin dry, and after column purification, the red powder is the iridium complex Ir-OH compound 3 Yield: 45%.
[0070] Step 4. Synthesis of mSiO 2 / CuS / Ir NPS, mix 3 mg Ir complex, 1.5 μL 3-mercaptopropyltrimethoxysilane and 1.5 mL tetrahydrofuran, add 2.3 μL 0.1M benzoin dimethyl ether tetrahydrofuran solution, and illuminate under ultraviolet light After 60 minutes, disperse the material obtained in step 3 in 20 mL of ethanol, adjust the pH to alkaline, add the lighted solution to the above solution, and heat at 25°C overnight to obtain the target product. The UV absorption figure of th...
Embodiment 3
[0072] Same as Example 1, the difference lies in Step III and Step 4 in Step 1.
[0073] In step 1, III) take 680 mg of the product obtained in step II, 130 mg of 3-hydroxy-2-pyridinecarboxylic acid and 300 mg of sodium carbonate in a 100 mL single-necked bottle with a stirrer, blow nitrogen, add 30 mL of ethylene glycol ether, and at 110 ° C, Reflux and stir for 12 hours, after extraction, spin dry, and after column purification, the red powder is the iridium complex Ir-OH compound 3 Yield: 55%.
[0074] Step 4. Synthesis of mSiO 2 / CuS / Ir NPS, mix 3 mg Ir complex, 1.5 μL 3-mercaptopropyltrimethoxysilane and 1.5 mL tetrahydrofuran, add 2.3 μL 0.1M benzoin dimethyl ether tetrahydrofuran solution, and illuminate under ultraviolet light For 40 minutes, disperse the material obtained in step 3 in 20 mL of ethanol, adjust the pH to alkaline, add the lighted solution to the above solution, and heat at 50°C overnight to obtain the target product. The SEM image obtained from the ...
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