Doxorubicin structure-containing star-shaped polymer and preparation method and use thereof

A technology of star-shaped polymer and doxorubicin, applied in medical preparations containing active ingredients, medical preparations with non-active ingredients, drug combinations, etc., can solve problems such as short half-life, high toxicity, and application limitations. Achieving superior efficacy, extended half-life, and ease of dissolution

Inactive Publication Date: 2014-07-09
张雅珍
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0003] Doxorubicin is currently widely used, but it often needs to be turned into a salt from a clinical point of view. For example, the common medicinal form of doxorubicin is doxorubicin hydrochloride, which needs to be turned into hydrochloride. Its solubility is very low, it cannot be converted into salt form, so it cannot be used
After becoming hydrochloride, the pharmacodynamic function of doxorubicin is greatly reduced, so this brings great diffi

Method used

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  • Doxorubicin structure-containing star-shaped polymer and preparation method and use thereof
  • Doxorubicin structure-containing star-shaped polymer and preparation method and use thereof
  • Doxorubicin structure-containing star-shaped polymer and preparation method and use thereof

Examples

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Effect test

Embodiment 1

[0042] 1) The mixture of 80 g of sebacic acid in 800 ml of acetic anhydride is refluxed to form acetyl-sebacic acid;

[0043] 2) Mix the 10g product of step 1) and 3-arm polyethylene glycol ending in a hydroxyl group into a flask, and conduct a solution polymerization reaction under reduced pressure at 180°C for 1 hour; when the polymer is cooled to room temperature, dissolve it with chloroform, and use petroleum washed with ether and dried;

[0044] 3) Put 120mg of doxorubicin and the 800mg polymer of step 2 into 8ml of dimethyl sulfoxide and 12ml of dichloromethane solution for 48 hours; ultrasonic for 3 minutes; then place in an oven for 1 hour; Stir at a high speed in a homogenizer at 20°C for 3 minutes, then put into 1% polyvinyl alcohol solution and stir at 600 rpm for 2 hours; collect by centrifugation and freeze-dry to obtain the final star-shaped polymer nanoparticles.

Embodiment 2

[0046] 1) The mixture of 100 g of sebacic acid in 900 ml of acetic anhydride is refluxed to form acetyl-sebacic acid;

[0047] 2) Mix the product of step 1) and 18 g of 3-arm polyethylene glycol ending in a hydroxyl group into a flask, and conduct a solution polymerization reaction under reduced pressure at 180° C. for 1 hour; when the polymer is cooled to room temperature, dissolve it with chloroform, and use petroleum washed with ether and dried;

[0048] 3) Put 200mg of doxorubicin and 1000mg of the polymer in step 2 into 6ml of dimethyl sulfoxide and 14ml of dichloromethane solution for 24 hours; ultrasonic for 2 minutes; then put in an oven for 2 hours; at minus 10 degrees Stir in a medium homogenizer at an ultra-high speed for 2 minutes, then put into 10% cholic acid solution and stir at 600 rpm for 3 hours; collect by centrifugation and freeze-dry to obtain the nanoparticles of the final product.

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Abstract

The invention discloses a doxorubicin structure-containing star-shaped polymer and a preparation method and use thereof. The doxorubicin coupled star-shaped polymer has a better effect on treatment of age-related macular degeneration compared with drugs or medicaments in other forms.

Description

technical field [0001] The invention discloses a star polymer containing a doxorubicin structure, a preparation method and an application of the polymer. Background technique [0002] Doxorubicin is an antimitotic and extremely cytotoxic drug. Doxorubicin can successfully inhibit a variety of malignancies, including acute leukemia, lymphoma, soft tissue and osteosarcoma, childhood malignancies, and adult solid tumors. Its mechanism of action is that the drug can penetrate into the cell and bind to the chromosome. The planar loop in the drug structure is inserted between base pairs to form a complex with DNA, which seriously interferes with DNA synthesis, DNA-dependent RNA synthesis, and protein synthesis. However, the concentration of doxorubicin required to produce an antiproliferative effect through this mechanism is higher than the concentration of the drug at the tumor site in clinical treatment. In addition, doxorubicin is also related to the redox effect, and can pa...

Claims

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Application Information

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IPC IPC(8): C08G65/48C08G63/91A61K47/48A61K31/704A61P27/02A61P9/10
Inventor 张雅珍李铁力白毅
Owner 张雅珍
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