Preparation method for micelle based on gadolinium ion-doped up-conversion luminescent nano-material
A nanomaterial and gadolinium ion technology is applied in the field of preparation of upconversion luminescent nanomaterial micelles based on gadolinium ion doping, which can solve problems such as low sensitivity, achieve high-sensitivity magnetic resonance, realize optical imaging dual-mode imaging, The effect of high optical imaging dual-modality imaging
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[0030] Embodiment 1: A preparation method of a gadolinium-doped upconversion luminescent nanomaterial micelle that can be used as a contrast agent for magnetic resonance imaging and can realize optical imaging of the present invention. The specific steps are as follows:
[0031] 1) Preparation of upconversion luminescent nanomaterials:
[0032] Prepared by pyrolysis method: ①Weigh 0.72807g (2.4mmol) YCl respectively 3 ·6H 2 O, 0.290925g (0.54mmol) YbCl 3 ·6H 2 O and 0.022902g (0.06mmol) ErCl 3 ·6H 2 After 0, transfer to a round-bottom three-necked flask with a volume of 100ml, measure 45ml of oleic acid and 22.5ml of octadecene in a volume ratio of 2:1, and heat the reaction system to 160°C under vigorous stirring with argon and maintain it for 30min; ② After cooling to room temperature naturally, 0.3 g NaOH and 0.44445 g NH were added dropwise. 410ml methanol solution of F was maintained at 50°C and closed and stirred for 30min; 3. Under argon atmosphere, the system was...
Example Embodiment
[0037] Example 2:
[0038] Accurately weigh 38.84 mg DSPE-PEG2000 and 9 mg mal-PEG-DSPE according to the molar ratio of 4:1, add 6 ml of chloroform, and ultrasonically disperse them uniformly, then add 0.5 ml of chloroform-dispersed OA-UCNP@Gd, and add 4 ml of deionized water. After the ultrasonic dispersion was uniform, the excess chloroform was evaporated by a rotary evaporator at a rotating speed of 50 rpm at 65 °C until it was clear and transparent. The final reaction system was ultrasonicated with a probe for 5 min, transferred to an ultrafiltration tube, and centrifuged at 5000 g for 20 min to obtain UCNP@PEG. .
Example Embodiment
[0039] Example 3:
[0040] Accurately weigh 54.0 mg DSPE-PEG2000 and 9 mg mal-PEG-DSPE according to the molar ratio of 6:1, add 6 ml of chloroform and disperse them uniformly by ultrasonic, then add 0.5 ml of chloroform-dispersed OA-UCNP@Gd, and add 4 ml of deionized water After the ultrasonic dispersion was uniform, the excess chloroform was evaporated by a rotary evaporator at a rotating speed of 50 rpm at 65 °C until it was clear and transparent. The final reaction system was ultrasonicated with a probe for 5 min, transferred to an ultrafiltration tube, and centrifuged at 5000 g for 20 min to obtain UCNP@PEG. .
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