A preparation method of polypeptide hydrogel for encapsulating medicine
A technology for hydrogels and drugs, applied in the field of preparation of polypeptide hydrogels, can solve the problems of long gelation time, several hours or even two or three days, poor water solubility of sequence polypeptides, etc., and achieves simple operation method and good repeatability. Effect
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Embodiment 1
[0031] The method of the present invention adopts the conventional solid-phase Fmoc method, that is, the monomer amino acid protected by Fmoc on the solid-phase resin is deprotected to expose the amino group, and forms a peptide bond with the carboxyl group of the amino acid in the solution through a condensation reaction, thereby linking the amino acid to the On the resin, the peptide chain is extended from the C-terminus to the N-terminus.
[0032] 1. Basic materials:
[0033] (1) Resin and linking molecule: The resin selected by the solid-phase Fmoc method is Rink Amide- resin. This kind of resin has very good swelling property, which can make the condensation reaction between the peptide chains better, and there is enough network space to meet the growing peptide chains. HBTU and HOBt are used as linking molecules to immobilize the polypeptide molecules on the resin.
[0034] (2) Monomer: The monomer used in the synthesis is a chemically modified α-amino acid.
[0035...
Embodiment 2
[0052]For the polypeptide hydrogel obtained by the method in Example 1, absorb 500 microliters of PBS buffer solution with a pH of 7.4 and a salt ion concentration of 0.01M on the upper layer of the hydrogel, then place it in a water bath at 37°C, and take out the release solution after 0.5h , and add 500 microliters of new PBS buffer under the same conditions, and replace the buffer again after 1 hour, and the replacement time doubles. Then, the absorbance of the release liquid was measured by an ultraviolet spectrophotometer, and the amount of doxorubicin hydrochloride was calculated according to Lambert-Beer's law, and the calculated contents of multiple release liquids were added to obtain the total release amount. And draw the total release amount-time graph according to the relationship between the total release amount and time. In addition, the PBS buffer conditions were selected as pH 5.5 0.01M and pH 6.5 0.01M, and the hydrochloric acid in the IKFQFHFD polypeptide hydr...
Embodiment 3
[0054] Select the PBS buffer conditions as: pH7.4 0.01M, pH7.4 0.025M and pH7.4 0.05M, and measure the relationship between the amount of doxorubicin hydrochloride released in the IKFQFHFD polypeptide hydrogel and time at 37 ° C, the steps With embodiment 2.
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