Up-conversion bionic complex as well as preparation method and application in weak ultraviolet conversion
A complex and particle conversion technology, which is applied in the direction of luminescent/biological dyeing preparations, preparations for in vivo tests, drug combinations, etc., can solve problems such as adverse consequences, damage to irradiated parts, and traumatic unfavorable multiple times. Achieve the effect of increasing concentration and avoiding tissue damage
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Embodiment 1
[0080] 1) Add β-NaYF 4 and YCl with EDTA 3 , YbCl 3 , TmCl 3 (Molar ratio 79:20:1) aqueous solution is fully mixed to form EDTA-rare earth element chelate emulsion, drop into NaF solution, heat at 200°C for 18 hours after rapid stirring, and rinse with deionized water and ethanol repeatedly after cooling to room temperature Precipitation, drying, annealing and crystallization at 400°C in a nitrogen atmosphere to obtain organic upconversion particles.
[0081] 2) The reference for the method of compounding upconversion particles with sensitizers and activators is Han J, etal. Amplification of Circularly Polarized Luminescence through Triplet–Triplet Annihilation-Based Photon Upconversion. Journal of the American Chemistry Society. 9783–9786. and Liu Q, et al. Highly Photostable Near-IR-Excitation Upconversion Nanocapsules Based on Triplet–Triplet Annihilation for in Vivo Bioimaging Application. ACS Applied Materials and Interfaces. 2018, 10(12):9883-9888. The sensitizer is ...
Embodiment 3
[0085] Construct and connect fluorescent probes for miR-155 detection: Based on the ssDNA sequence 5′-AAA CCC CTATCA CGA TTA-3′ for miR-155 detection, a double-stranded nucleotide chain was constructed, and the two ends of the two chains were connected to Cy5. 5 and BHQ-3 Black Hole Quencher. According to the FRET principle, when miR-155 binds to the ssDNA sequence, Cy5.5 is separated from BHQ-3 to release a fluorescent signal. The biodegradable dendritic polymer PAMAM is connected to the surface of the prepared core-shell type upconversion particles by carbodiimide chemical technology, and the miR-155 fluorescence detection probe is connected by using the positive charge adsorption of PAMAM.
Embodiment 4
[0087] Neutrophil membrane bionic packaging: collect peripheral blood from mice, collect neutrophils by Percoll gradient centrifugation, break up the cells, filter them with a filter with a pore size of 1 μm, and then centrifuge at 3200g. Centrifuge, collect the supernatant of the two centrifuges, filter and centrifuge at 20,000g for 20-30 minutes, then centrifuge the supernatant at 100,000g for 5 minutes, resuspend the pellet with 10mM Tris-HCl (pH7.5) and 1mM EDTA, Collect neutrophil membranes.
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