A kind of biological nanocomposite material and its synthesis method and application
A bio-nano and composite material technology, 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 effects of good drug-carrying capacity, uniform size distribution, and simple operation.
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Embodiment 1
[0141] Example 1: Synthesis of iron ion two-photon fluorescent probe
[0142] 1 mmol of tetrabutylammonium hydrogen sulfate, 22 mmol of 4-diethylaminobenzaldehyde and 10 mmol of 2-amino-4,6-dimethylpyrimidine were refluxed in 50 mL of 5M NaOH solution for 2 hours. The orange product was obtained by rotary evaporation and 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 of ruthenium trichloride, 112 mmol of phenanthroline and 3.7 mmol of lithium chloride were refluxed in 25 mL of DMF for 8 hours. Acetone was then added to the reaction mixture, which was cooled at 4°C overnight, the product Ru(phen) 2 Cl 2 Used without further purification. 12mmol Ru(phen) 2 Cl 2 and 10 mmol of dipyrido[3,2-A:2'.3'-C]phenazine in 1:1 aqueous methanol at reflux for 4 hours. The apparatus was cooled to room temperature, ammonium hexafluorophosphate was added to precipitate the product out of solution and the crude product was obtained by filtration. Purification by column chromatography (dichloromethane:acetonitrile=4:1) and recrystallization (ethanol:water=90:10) gave red-orange crystals.
Embodiment 3
[0145] Example 3: Synthesis of multifunctional bio-nanocomposites
[0146] In pH=7.4 PBS buffer solution, 20 μg of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride was added to 5 mL of 10 μg / mL copper sulfide nanospheres, stirred for 2 hours, and then 20 μg of N-hydroxysuccinimide was added and stirred for half an hour, and then 100 μL of the 50 μg / mL iron ion two-photon fluorescent probe prepared in Example 1 of the present invention was added to the mixture overnight with stirring. The product was collected by centrifugation and purified by washing several times with deionized water, then resuspended in 5 mL of PBS buffer 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 several washes with deionized water, and then resuspended in 5 mL of PBS buffer pH=7.4....
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