Preparation with contrast-enhanced ultrasound and photothermal therapy properties, preparation method and application thereof
A technology of photothermal therapy and contrast-enhanced ultrasound, which is applied to echo/ultrasound imaging agents, medical preparations containing active ingredients, and pharmaceutical formulations, etc., which can solve the problems of wide particle size distribution of microcapsules, cumbersome preparation process, and ineffective matching. , to achieve the effect of improved light-to-heat conversion efficiency, simple preparation process, and excellent mechanical properties
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Embodiment 1
[0033] Embodiment 1: A preparation method of a preparation with ultrasound contrast and photothermal therapy properties, comprising the following steps:
[0034] (1) Pipette 0.25 mL of polystyrene microsphere water suspension (590 nm, 5wt%) and disperse it into a mixed solvent composed of 7 mL of deionized water and 30 mL of isopropanol, sonicate in a water bath for 5 min, and then add ammonia water to adjust the pH value to 10.8, add 0.2 mL ethyl orthosilicate, stir and hydrolyze for 30 min, then add 0.02 mL of 3-aminopropyltriethoxysilane to continue the reaction for 3 h, deionized water and ethanol are alternately centrifuged and washed three times to obtain surface amino groups Crystallized core-shell microspheres;
[0035](2) Transfer the core-shell microspheres prepared in step (1) to a THF hot solvent at 80 °C, stir for 8 h, and centrifuge and wash three times with deionized water to obtain hollow SiO with surface amination. 2 ball;
[0036] (3) Add citrate-modified g...
Embodiment 2
[0041] Embodiment 2: A preparation method of a preparation with ultrasound contrast and photothermal therapy properties, comprising the following steps:
[0042] (1) Pipette 0.5 mL of polystyrene microsphere suspension (1200 nm, 2.5 wt%) and disperse it into a mixed solvent consisting of 7 mL of deionized water and 30 mL of isopropanol, ultrasonicate in a water bath for 5 min, and then add ammonia water to adjust the pH value to 11.0, add 0.4 mL ethyl orthosilicate, stir and hydrolyze for 30 min, then add 0.1 mL of 3-aminopropyltriethoxysilane to continue the reaction for 3 h, deionized water and ethanol are alternately centrifuged and washed three times to obtain the surface amino group Crystallized core-shell microspheres;
[0043] (2) Transfer the core-shell microspheres prepared in step (1) to a THF hot solvent at 80 °C, stir for 8 h, and centrifuge and wash three times with deionized water to obtain hollow SiO with surface amination. 2 ball;
[0044] (3) Add citrate-mod...
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