Preparation method of octreotide-coupled nano-chitosan molecular beacon
A nano-chitosan and molecular beacon technology, applied in the field of biomedicine, can solve problems such as poor specificity or stability, harsh process conditions, and complicated preparation methods, and achieve high specificity, high transfection efficiency, and stability Good results
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Embodiment 1
[0025] The nano-chitosan and the molecular beacon were mixed in the PBS buffer of pH 6.0 according to the mass ratio of 7:1, and vortexed for 60 s, and stood at room temperature for 60 min to obtain the nano-chitosan molecular beacon complex; Add 1.0% glutaraldehyde solution dropwise to the nano-chitosan molecular beacon complex, the mass ratio of the glutaraldehyde solution to the nano-chitosan molecular beacon complex is 1000:1, and mix by stirring for the first time Reaction for 1.5h, the stirring speed for the first time is 150rpm, after the reaction, go through the microdialysis column for the first time to dialysis for 1h to remove unbound glutaraldehyde; then according to the mass ratio of octreotide and nano-chitosan molecular beacon complex is 100: Add octreotide at a ratio of 1, carry out the second stirring and mixing reaction for 4 hours, the second stirring speed is 150rpm, after the reaction, the unbound octreotide is removed by the second dialysis of the microdia...
Embodiment 2
[0026] Example 2: The difference from Example 1 is that the chitosan nanometer and the molecular beacon are in a mass ratio of 10:1, and a nano-chitosan molecular beacon complex coupled with octreotide with a particle size of 40nm to 80nm is finally obtained .
Embodiment 3
[0027] Example 3: The difference from Example 1 is that the chitosan nanometer and the molecular beacon are in a mass ratio of 8:1, and finally a nano-chitosan molecular beacon complex coupled with octreotide with a particle size of 45nm to 60nm is obtained .
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