Preparation method of CT nano contrast agent namely low-algebraic tree-shaped macromolecule-coated gold nano particles with liver cancer targeting function
A technology of dendritic macromolecules and nano-contrast agents, which can be used in the preparation of X-ray contrast agents, medical preparations of non-active ingredients, pharmaceutical formulations, etc., and can solve the problems of undiscovered CT imaging applications, etc.
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Embodiment 1
[0065] (1) The second generation polyamide-amine dendrimers (G2.NH 2) 16.28 mg was dissolved in 3.2 mL of dimethyl sulfoxide, and 17.04 mL of a dimethyl sulfoxide solution of fluorescein isothiocyanate (0.4 mg / mL) was added while stirring. After reacting at room temperature for 24 hours, the reaction solution was dialyzed against distilled water (6 times, 2 L / time), and dialyzed for 3 days. Then freeze-dry to obtain fluorescein isothiocyanate-modified dendrimer, and store at -20°C. 1 The H NMR test results showed that the chemical shift peaks at 2.0-3.7ppm and 6.3-8.0ppm in the spectrum corresponded to the characteristic peaks of dendrimer and fluorescein isothiocyanate, respectively. According to the calculation of the integral area, about 2.5 fluorescein isothiocyanate molecules are modified on the surface of each dendrimer (attached figure 1 a).
[0066] (2) 32.25 mg of lactobionic acid was dissolved in 3.75 mL of disodium hydrogen phosphate-sodium dihydrogen phosphate b...
Embodiment 2
[0069] 34.63 mg of fluorescein isothiocyanate-labeled and lactobionic acid-modified pegylated dendrimer was dissolved in 6.00 mL of distilled water. Then, 211.89 μL (30 mg / mL) of an aqueous chloroauric acid solution was added with stirring. After magnetic stirring for 10 min, 291.94 μL (10 mg / mL) of sodium borohydride solution pretreated in an ice bath was added and reacted at room temperature for 3 h. After the reaction, the resulting solution was dialyzed against distilled water (6 times, 2 L / time) for 3 days. Freeze-drying was then carried out to obtain the final product, which was stored at -20°C. The UV-Vis test results show that there is an absorption peak at about 510nm in the spectrogram (attached figure 2 ), which is the superposition of the surface plasmon resonance peak of nano-gold and the absorption peak of fluorescein, which indicates that gold nanoparticles were successfully prepared in the system. TEM test results show that: the prepared gold nanoparticles ...
Embodiment 3
[0071] Configure the aqueous solution (0.5 mg / mL) of the product obtained in Example 2, place it at different temperatures for half an hour, measure its ultraviolet spectrum, and determine the stability of the product at different temperatures. Find, under different temperature (4-50 ℃) condition, the ultraviolet spectrum of the obtained product of embodiment 2 does not have obvious shift and change, shows that it has good stability (attachment image 3 ).
[0072] The product obtained in Example 2 was prepared as a 0.5 mg / mL aqueous solution, and its pH value (5.0, 6.0, 7.0, 8.0) was adjusted with 0.1 M hydrochloric acid or sodium hydroxide. After standing at room temperature for 20 minutes, carry out the ultraviolet test. The UV spectra of this product under different pH values (5.0-8.0) have not been shifted and changed due to particle agglomeration through comparative analysis, indicating that it has good stability (attached Figure 4 ).
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