Preparation method and application of temperature-responsive reversible hydrogel
A temperature-responsive, hydrogel technology, applied in non-active ingredients medical preparations, active ingredients-containing medical preparations, pharmaceutical formulas, etc. Realize problems such as "sol-gel reversible transformation, and achieve the effect of simple and easy implementation, efficient loading, and wide sources.
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[0027] An embodiment of the present invention provides a method for preparing a temperature-responsive reversible hydrogel, including:
[0028] S1: Prepare an aqueous solution of a polypeptide capable of self-assembling to form a one-dimensional nanostructure. The concentration of the polypeptide in the aqueous solution is greater than its self-assembly critical concentration, and place it to complete the self-assembly.
[0029] In this step, the self-assembled polypeptide self-assembles into a one-dimensional nanostructure. Due to its amino acid composition, it has good biocompatibility and low toxicity. This structure can also provide surface groups or hydrophobic internal cavities to bind drug molecules. and loading. In this step, peptides with strong assembly ability are self-assembled above a certain concentration to form long nanofibers, nanotubes and other assembly structures. It can be understood that the polypeptide molecules that can form one-dimensional nanostructure...
Embodiment
[0043] The preparation concentration is 10.0mM (greater than I 3 K critical self-assembly critical concentration) I 3 K aqueous solution, the pH of the aqueous solution is 4.5±0.5, and it is placed for more than 1 day to make it complete self-assembly, and the self-assembled nanofibrous structure is as follows figure 1 shown;
[0044] Poly-N-isopropylacrylamide (PNIPAM) was dissolved in Tris buffer solution at a concentration of 20 mg / mL, left overnight, and stirred to obtain a poly-N-isopropylacrylamide solution.
[0045] The above self-assembled I 3 K solution and the above poly-N-isopropylacrylamide solution were mixed in equal volumes at 30°C, stirred for 10 minutes, and mixed evenly to obtain a final solution. The concentration of the polypeptide in the final solution was greater than its self-assembly critical concentration while maintaining uniformity. Dispersion concentration, the concentration of poly-N-isopropylacrylamide in the final solution is greater than 1.0m...
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