Targeting fluorescent-magnetic nano-material as well as preparation method and application thereof
A magnetic nano-targeted technology, applied in the field of nano-biomedical materials, can solve the problems of weakening overall performance, application of bound fluorescent magnetic composite nanoparticles, toxicity, etc., and achieves good magnetic separation, simple synthesis method, and biocompatibility. Good results
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Embodiment 1
[0027] 1. Zn 0.4 Fe 2.6 o 4 Preparation of NPs
[0028] FeSO 4 ·(NH 4 ) 2 SO 4 ·6H 2 O and ZnSO 4 Dissolve in 20ml of water so that the precursor reaches 1.73×10 -3 mol Fe 2+ and 2.67×10 -4 mol Zn 2+ the goal of. Next, mix 10ml of oleic acid, 10ml of absolute ethanol and 1g of NaOH, and stir magnetically at room temperature until a uniform solution is obtained. Furthermore, the precursor Fe 2+ and Zn 2+ The mixed solution was poured into the homogeneous solution, and after stirring for a few minutes, the mixed solution turned dark brown. Finally, the solution was transferred into a 50ml reaction kettle, sealed, and heated at 230 degrees for 15 hours. After the reaction, cool to room temperature. The product is deposited at the bottom of the kettle, and the nanoparticles are dispersed in cyclohexane and taken out. Add ethanol to the n-hexane dispersed with nanoparticles to precipitate the nanoparticles, and finally wash the nanoparticles repeatedly with et...
Embodiment 2
[0035] Steps 1 and 2 are the same as in Example 1,
[0036] 3. RGERPPR-PEG-DSPE wrapped Zn 0.4 Fe 2.6 o 4 Preparation of NPs and CQDs
[0037] Dissolve RGERPPR-PEG-DSPE in 5ml of chloroform and transfer to a 50ml eggplant bottle, then add 5ml of Zn dispersed in n-hexane 0.4 Fe 2.6 o 4 NPs and CQDs (Zn 0.4 Fe 2.6 o 4 The ratio of the amount of NPs to CQDs is 2:1), so that RGERPPR-PEG-DSPE and Zn 0.4 Fe 2.6 o 4 The ratio of the mass sum of NPs and CQDs is 2:1, and the ultrasonic mixing is uniform. Finally, 5ml of deionized water was slowly added to the mixture. At a temperature of 70° C., rotary evaporation was performed for 15 minutes until the chloroform and n-hexane were completely evaporated. Excess empty liposome micelles were removed by magnetic separation, and larger aggregates were removed by centrifugation at 3000g, and the product was redispersed in deionized water.
[0038] Characterized RGERPPR-PEG-DSPE wrapped Zn 0.4 Fe 2.6 o 4 The water and ki...
Embodiment 3
[0040] Steps 1 and 2 are the same as in Example 1,
[0041] 3. RGERPPR-PEG-DSPE wrapped Zn 0.4 Fe 2.6 o 4 Preparation of NPs and CQDs
[0042] Dissolve RGERPPR-PEG-DSPE in 5ml of chloroform and transfer to a 50ml eggplant bottle, then add 5ml of Zn dispersed in n-hexane 0.4 Fe 2.6 o 4 NPs and CQDs (Zn 0.4 Fe 2.6 o 4 The ratio of the amount of NPs to CQDs is 1:2), so that RGERPPR-PEG-DSPE and Zn 0.4 Fe 2.6 o 4 The ratio of the mass sum of NPs and CQDs is 2:1, and the ultrasonic mixing is uniform. Finally, 5ml of deionized water was slowly added to the mixture. At a temperature of 70° C., rotary evaporation was performed for 15 minutes until the chloroform and n-hexane were completely evaporated. Excess empty liposome micelles were removed by magnetic separation, and larger aggregates were removed by centrifugation at 3000g, and the product was redispersed in deionized water.
[0043] Characterized RGERPPR-PEG-DSPE wrapped Zn 0.4 Fe 2.6 o 4 The water and ki...
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