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Adriamycin and indocyanine green co-loaded polysaccharide-based nanoparticles as well as preparation method and application of adriamycin and indocyanine green co-loaded polysaccharide-based nanoparticles

A technology of indocyanine green and nanoparticles, which can be applied to medical preparations with non-active ingredients, medical preparations containing active ingredients, wave energy or particle radiation treatment materials, etc. Controllable release and other issues, to achieve simple purification process, improve tumor treatment effect, and good biocompatibility

Active Publication Date: 2021-03-12
XI AN JIAOTONG UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

However, most nanoparticles will leak during drug delivery, and it is difficult to achieve rapid and controlled release of drugs

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  • Adriamycin and indocyanine green co-loaded polysaccharide-based nanoparticles as well as preparation method and application of adriamycin and indocyanine green co-loaded polysaccharide-based nanoparticles
  • Adriamycin and indocyanine green co-loaded polysaccharide-based nanoparticles as well as preparation method and application of adriamycin and indocyanine green co-loaded polysaccharide-based nanoparticles
  • Adriamycin and indocyanine green co-loaded polysaccharide-based nanoparticles as well as preparation method and application of adriamycin and indocyanine green co-loaded polysaccharide-based nanoparticles

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preparation example Construction

[0039] A method for preparing nanoparticles co-loaded with doxorubicin and indocyanine green in the present invention, first, doxorubicin and indocyanine green are respectively loaded on the formhylated hyaluronic acid and water-soluble On the chitosan, they are mixed in a certain proportion to form nanoparticles loaded with doxorubicin and indocyanine green, and then modified by layer-by-layer self-assembly process to form aldylated hyaluronic acid, water-soluble chitosan and Aldylation of hyaluronic acid with targeting ligands to yield polysaccharide-based nanoparticles co-loaded with doxorubicin and indocyanine green. Specifically include the following steps:

[0040] (1) Preparation of aldoxylated hyaluronic acid nanoparticles loaded with doxorubicin: using sodium periodate oxidation method to synthesize aldylated hyaluronic acid with an oxidation degree of 40% to 100% or 5% to 20%, wherein The formhylated hyaluronic acid with an oxidation degree of 40% to 100% is purifie...

Embodiment 1

[0059] (1) Preparation of aldylated hyaluronic acid nanoparticles loaded with doxorubicin: the sodium periodate oxidation method was used to synthesize aldylated hyaluronic acid (MW=8kDa) with a degree of oxidation of 40%, and the specific process was as follows: Add sodium periodate with a mass concentration of 1.0% hyaluronic acid aqueous solution to 0.4 times the molar amount of the hyaluronic acid structural unit, react in the dark for 8 hours at room temperature, then add 2 mL of ethylene glycol to terminate the reaction, and dialyze and purify in deionized water for 48 hours to obtain Formhylated hyaluronic acid with a theoretical oxidation degree of 40%;

[0060] Prepare this formhylated hyaluronic acid into a solution with a concentration of 6 mg / mL, and then add doxorubicin with a concentration of 2 mg / mL dropwise according to the mass ratio of doxorubicin to formylated hyaluronic acid at a ratio of 1:6. aqueous solution, reacted at room temperature for 0.5 hours, the...

Embodiment 2

[0076] (1) Preparation of aldylated hyaluronic acid nanoparticles loaded with doxorubicin: the sodium periodate oxidation method was used to synthesize aldylated hyaluronic acid (MW=8kDa) with a degree of oxidation of 40%, and the specific process was as follows: Add sodium periodate with a mass concentration of 1.0% hyaluronic acid aqueous solution to 0.4 times the molar number of hyaluronic acid repeating structural units, react in the dark for 24 hours at room temperature, then add 2 mL of ethylene glycol to terminate the reaction, and dialysis and purify in deionized water for 72 hours. The aldehydlated hyaluronic acid with a theoretical oxidation degree of 40% is obtained;

[0077] Prepare this formhylated hyaluronic acid into a solution with a concentration of 6 mg / mL, and then add doxorubicin with a concentration of 2 mg / mL dropwise according to the mass ratio of doxorubicin to formylated hyaluronic acid at a ratio of 1:5. aqueous solution, after reacting at room temper...

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Abstract

The invention relates to adriamycin and indocyanine green co-loaded polysaccharide-based nanoparticles as well as a preparation method and application thereof. The method comprises the steps: placingthe adriamycin and indocyanine green co-loaded polysaccharide-based nanoparticles in a PBS buffer solution with a pH value of 6.0-6.4; dropwise adding an aldehyde hyaluronic acid solution under an icebath ultrasonic condition; after reaction, carrying out centrifugal washing, and then resuspending the nanoparticles in deionized water; dropwise adding a water-soluble chitosan solution with a concentration under an ice-bath ultrasonic condition, carrying out centrifugal washing after the reaction, re-suspending in a PBS buffer solution, finally dropwise adding an aldehyde hyaluronic acid solution with a targeting ligand, carrying out centrifugal washing after the reaction is carried out for 0.5-24 hours, and thus obtaining the adriamycin and indocyanine green co-loaded polysaccharide-basednanoparticles. The prepared nanoparticles are formed through a self-assembly process, the preparation method is simple, raw material sources are rich, drug loading and nanoparticle forming are achieved synchronously, the nanoparticles are good in stability under the neutral condition, and the purification process is simple.

Description

technical field [0001] The invention belongs to the field of biological materials, and in particular relates to a polysaccharide-based nanoparticle co-carrying doxorubicin and indocyanine green, a preparation method and application thereof. Background technique [0002] Cancer is a major challenge faced by human beings, and chemotherapy is one of the main means of cancer treatment. Doxorubicin is a broad-spectrum anti-tumor chemotherapy drug, which kills tumor cells by inserting and inhibiting DNA biosynthesis, and is suitable for a variety of tumor treatments. However, doxorubicin, like other chemotherapeutic drugs, has problems such as high toxicity and side effects, and easy induction of drug resistance in cancer cells, which leads to the failure of cancer treatment. To overcome these shortcomings, combination therapy based on different treatment modalities provides a new idea for cancer treatment. [0003] Phototherapy has the advantages of non-invasiveness, remote con...

Claims

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Application Information

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IPC IPC(8): A61K47/61A61K47/69A61K41/00A61K31/704A61P35/00
CPCA61K47/6939A61K47/61A61K41/0057A61K41/0052A61K31/704A61P35/00A61K2300/00
Inventor 钱军民王亚萍胥伟军侯光晖
Owner XI AN JIAOTONG UNIV