Amphiphilic nano-medicine and its preparation method and application
A nano-drug, amphiphilic technology, applied in nano-drugs, drug combinations, nano-technology, etc., can solve problems such as affecting drug efficacy, and achieve the effects of easy repeatability and characterization, strong hydrophobicity, and low bioavailability
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Embodiment 1
[0028] The cleavable disulfide bond was connected to the amino-functionalized PEG through Michael addition reaction to prepare a terminal-functionalized and amphiphilic PEG molecule (compound I). The specific route is as follows:
[0029]
[0030] Then compound I is reacted with Sorafenib a part amide hydrogen to obtain the final compound SCNS, the specific route is as follows:
[0031]
[0032] The results of the compound SCNS hydrogen spectrum are as follows figure 1 shown. The results showed that: after Michael addition reaction, Sorafenib was successfully connected to PEG.
Embodiment 2
[0034] The water solubility of the SCNS synthesized in Example 1 was compared with that of Sorafenib, and the results are shown in Table 1.
[0035] Table 1. Comparison of water solubility of SCNS and Sorafenib
[0036]
[0037]
[0038] The results showed that Sorafenib was almost completely insoluble in water, while the improved compound SCNS had good water solubility.
Embodiment 3
[0040] The morphology of SCNS in aqueous solution was measured for particle size, the results are as follows figure 2 shown. Experimental results show that the obtained compound forms nanoparticles of about 200nm in water solubility, which is beneficial for entering cells and intravenous administration.
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