Biological nanocomposite material, and synthesis method and application thereof
A technology of bio-nano and composite materials, which is applied in the field of bio-nano-composite materials and their synthesis, can solve problems such as interactions that have not been clearly reported, and achieve the effect of high photostability
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Embodiment 1
[0141] Embodiment 1: the synthesis of iron ion two-photon fluorescent probe
[0142] 1 mmol tetrabutylammonium bisulfate, 22 mmol 4-diethylaminobenzaldehyde and 10 mmol 2-amino-4,6-dimethylpyrimidine were refluxed in 50 mL 5M NaOH solution for 2 hours. The orange product was obtained by rotary evaporation, and the pure material was obtained by column chromatography (ethyl acetate:petroleum ether=1:1).
Embodiment 2
[0143] Example 2: Synthesis of α-synuclein two-photon fluorescent probe
[0144] 56 mmol ruthenium trichloride, 112 mmol o-phenanthroline and 3.7 mmol lithium chloride were refluxed in 25 mL DMF for 8 hours. Acetone was then added to the reaction mixture, which was cooled overnight at 4°C, and the product Ru(phen) 2 Cl 2 Used without further purification. 12mmol Ru(phen) 2 Cl 2 And 10mmol dipyrido[3,2-A:2'.3'-C]phenazine was refluxed in 1:1 methanol aqueous solution for 4 hours. The apparatus was cooled to room temperature, ammonium hexafluorophosphate was added to precipitate the product from solution and filtered to give crude product. Purification by column chromatography (dichloromethane:acetonitrile=4:1) and recrystallization (ethanol:water=90:10) gave red-orange crystals.
Embodiment 3
[0145] Embodiment 3: the synthesis of multifunctional biological nanocomposite material
[0146] In PBS buffer solution with pH=7.4, 20 μg 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride was added to 5 mL of 10 μg / mL copper sulfide nanospheres and stirred for 2 hours, then 20 μg of N-hydroxysuccinimide was added and stirred for half an hour, after which 100 μL of 50 μg / mL iron ion two-photon fluorescent probe prepared in Example 1 of the present invention was added to the mixture overnight under stirring. The product was collected by centrifugation and purified by washing several times with deionized water, then resuspended in 5 mL of PBS buffer solution, pH=7.4. Finally, 100 μL of 50 μg / mL α-synuclein two-photon fluorescent probe prepared in Example 2 of the present invention was added to the solution and stirred overnight at room temperature. The resulting product was collected by centrifugation, purified by washing several times with deionized water, and then r...
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