A kind of amino acid-chitosan nano drug loading system, its preparation method and application
A technology of chitosan nanometer and drug-loading system, which is applied in the fields of pharmaceutical formulations, nervous system diseases, and cardiovascular system diseases, etc. Reduce the effect of ischemic perfusion injury
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[0046] The preparation method of the amino acid-chitosan nano-loading system provided by the invention comprises the following steps:
[0047] (1) Dissolving chitosan in deionized water and configuring a concentration of chitosan is a chitosan solution of 10-50 mg / mL;
[0048] (2) To the chitosan solution prepared in step (1), add 10-100 mg / mL of amino acid to be loaded, mix evenly, adjust the pH value between 5-7, and prepare a mixed solution;
[0049] (3) The mixed solution obtained in the step (2) is continuously stirred more than 30min, while adding concentration dropwise at 1-10mg / mL sodium tripolyphosphate (STPP) aqueous solution, making the mass ratio of chitosan and STPP at 100 ~150:1, the amino acid-chitosan nanometer drug delivery system provided by the invention is prepared.
[0050] Among them, the concentration of chitosan affects the morphology of nanoparticles to a certain extent. If it is too low, it will not be able to form nanoparticles, and if it is too hig...
Embodiment 1
[0065] An amino acid-chitosan nanometer drug-carrying system, which comprises chitosan nanospheres and amino acid active ingredients packaged therein; the chitosan nanospheres contain oligomeric chitosan And sodium tripolyphosphate; the average particle size is about 266nm, the Zeta potential is about 14mV, the drug loading is about 29%, the amino acid encapsulation rate is about 39%, and the total release in vitro is about 58% within 3 days.
[0066] The Mw of the oligomeric chitosan is 800-1000, and the degree of deacetylation is ≥93%.
[0067] The amino acid active ingredient is: proline.
[0068] The preparation method of the amino acid-chitosan nano-loading system provided by the present embodiment comprises the following steps:
[0069] (1) dissolving chitosan in deionized water and configuring a concentration of chitosan is a chitosan solution of 10 mg / mL;
[0070] (2) To the chitosan solution prepared in step (1), add 10 mg / mL of amino acid to be loaded, mix evenly, ...
Embodiment 2
[0074] An amino acid-chitosan nano drug-carrying system, which comprises chitosan nano-microspheres and amino acid active ingredients packaged therein; And sodium tripolyphosphate; the average particle size is about 227nm, the Zeta potential is about 16mV, the drug loading is about 28%, the amino acid encapsulation rate is about 40%, and the total release in vitro is about 55% within 3 days.
[0075] The Mw of the oligomeric chitosan is 800-1000, and the degree of deacetylation is ≥93%.
[0076] The amino acid active ingredient is: proline.
[0077] The preparation method of the amino acid-chitosan nano-loading system provided by the present embodiment comprises the following steps:
[0078](1) dissolving chitosan in deionized water and configuring a concentration of chitosan is a chitosan solution of 10 mg / mL;
[0079] (2) To the chitosan solution prepared in step (1), add 10 mg / mL of amino acid to be loaded, mix evenly, adjust the pH value between 5-7, and prepare a mixed ...
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