Sensing material based on up-conversion nanoparticle and preparation method of sensing material
A nanoparticle and sensing material technology, which is applied in the field of preparation of upconversion nanoparticle sensing materials, can solve the problems of lack of specificity and inability to image target cells, and achieve uniform particle size, high selectivity, and broad application prospects Effect
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Embodiment 1
[0032] The invention provides a method for preparing a sensing material based on upconversion nanoparticles, and the specific preparation route is as follows: figure 1 Shown:
[0033] (1) Weigh 0.78mmol of yttrium acetate, 0.2mmol of ytterbium acetate and 0.02mmol of erbium acetate and dissolve them in 6mL of oleic acid and 17mL of octadecene. The mixture is heated to 160°C to form a transparent solution, which is naturally cooled to room temperature. Add 2.5mmol NaOH and 4mmol NH dropwise 4 A solution of F in 10 mL of methanol was stirred at room temperature for 30 min. Then, methanol was gradually removed by heating. After vacuuming at 100°C for 10 minutes, it was heated to 300°C under the protection of argon and maintained for 1h. After the resulting solution was naturally cooled, the oil-soluble up-converting nanoparticles were precipitated in ethanol;
[0034] (2) Disperse 100 mg of the above-prepared up-converting nanoparticles in 3 mL of toluene for later use. Weigh...
Embodiment 2
[0045] To study the adsorption performance of the sensing material (such as Figure 7 shown). Add 2.5 mg of UCNPsMIP or UCNPsNIP into a 4 mL centrifuge tube, and then add 2 mL of cytochrome C (PBS, pH 7.4) at concentrations of 4, 8, 12, 16, 20, and 24 μM. The mixture was shaken at room temperature for a period of time, and then its fluorescence value was measured with a fluorescence spectrophotometer connected with a 980nm exciter. From Figure 7 It can be seen that, with the increase of cytochrome C concentration, the fluorescence intensity weakens, and at the same concentration of cytochrome C, the fluorescence quenching of UCNPsMIP is greater than that of UCNPsNIP.
Embodiment 3
[0047] The dynamic performance of the sensing material was studied. Weigh 2.5 mg of the UCNPsMIP prepared in Example 1 and place it in a 4 mL centrifuge tube, then add 2 mL of 8 μM cytochrome C (PBS, pH 7.4), shake at room temperature for 0.5, 1, 2, 4, 6, 8, After 10, 12, and 14 hours, measure the fluorescence value with a fluorescence spectrophotometer connected with an external 980nm exciter. Such as Figure 8 As shown, the adsorption of UCNPsMIP to the target reached equilibrium in 10 h.
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