Carrier polypeptide for forming medical compositions and preparation method and application of carrier polypeptide
A technology for carrier polypeptides and drugs, applied in chemical instruments and methods, non-active components of polymer compounds, peptides, etc., can solve the problems of low bioavailability, short half-life, poor stability, etc., to reduce drug intake and prolong concentration. time, the effect of reducing medical costs
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Embodiment 1
[0057] The preparation of embodiment 1 carrier polypeptide 1-4
[0058] Using the solid-phase peptide synthesis method of the Fmoc strategy, the CS 336X instrument produced by CSBio Company was used to synthesize carrier peptides 1-4. The method of synthesis was carried out according to the manufacturer's instruction manual.
[0059] The prepared polypeptide was purified using HPLC C18 semi-preparative column, and the mobile phase was acetonitrile. The polypeptide freeze-dried powder is obtained by desalting and freeze-drying.
Embodiment 2
[0060] Example 2 Complex of Small Molecule Drug and Carrier Polypeptide 1
[0061] Polar small-molecule drugs choose penicillin drug amoxicillin, according to the molar ratio (the following ratios are not indicated as the same molar ratio) the ratio of amoxicillin to carrier polypeptide 1 is 10:1.
[0062] Weigh amoxicillin, dissolve it in normal saline to form a 1mmol / L solution, mix thoroughly, weigh 0.1mmol carrier polypeptide 1, dissolve it in 1L of the above normal saline, mix well, and mix by ultrasonic at 4°C After 5 minutes, the complex solution was obtained and lyophilized.
Embodiment 3
[0063] The complex of embodiment 3GLP-1 polypeptide and carrier polypeptide 1
[0064] Weigh 0.3 mg of GLP-1 lyophilized powder, dissolve it in 1 ml of normal saline, mix well, weigh 3.3 mg of carrier polypeptide 1 lyophilized powder, dissolve it in the above GLP-1 normal saline, mix well, and °C, stirred for 3 hours, and freeze-dried to obtain a solid powder of the complex.
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