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Application of Heme Oxygenase-1 Inhibitor in Preparation of Drugs for Inhibiting Adriamycin Cardiotoxicity

A technology of heme oxygenase and cardiotoxicity, applied in drug combinations, pharmaceutical formulations, organic active ingredients, etc., can solve problems affecting the quality of life of patients, the mechanism of myocardial injury is not fully understood, and the clinical application of doxorubicin is limited.

Active Publication Date: 2020-06-19
ZHEJIANG UNIV
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  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

This not only greatly affects the quality of life of patients, but also greatly limits the clinical application of adriamycin.
[0003] The toxicity of doxorubicin to the heart is to cause myocardial damage in a cumulative and dose-dependent manner, but the mechanism of myocardial damage is still not fully understood

Method used

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  • Application of Heme Oxygenase-1 Inhibitor in Preparation of Drugs for Inhibiting Adriamycin Cardiotoxicity
  • Application of Heme Oxygenase-1 Inhibitor in Preparation of Drugs for Inhibiting Adriamycin Cardiotoxicity
  • Application of Heme Oxygenase-1 Inhibitor in Preparation of Drugs for Inhibiting Adriamycin Cardiotoxicity

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Embodiment Construction

[0015] The present invention will be further described below in conjunction with specific examples, but the protection scope of the present invention is not limited thereto.

[0016] 1. Materials and Methods

[0017] 1.1 Experimental animals

[0018] Six-week-old SPF grade C57BL / 6 male mice were purchased from Shanghai Slack Experimental Animal Co., Ltd. and raised in SPF environment. Standard diet AIN-76A (iron content 50 mg / Kg, Research Diets, Inc) was adapted to feeding for 2 weeks, and randomly divided into groups according to body weight, with 6-8 animals in each group.

[0019] 1.2 Drugs and treatment

[0020] Compounds zinc protoporphyrin (ZnPP) and doxorubicin (DOX) were purchased from Sigma-Aldrich Company. Doxorubicin was dissolved in saline, and zinc protoporphyrin was dissolved in dimethyl sulfoxide (DMSO). Doxorubicin was injected intraperitoneally once at 10 mg / kg body weight; zinc protoporphyrin was injected intraperitoneally one day before doxorubicin injec...

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Abstract

The invention discloses application of an HO (Heme Oxygenase)-1 inhibitor in preparing medicine for treating cardiotoxicity induced by anti-cancer medicine-doxorubicin. The HO-1 inhibitor is zinc protoporphyrin. According to the application disclosed by the invention, basis is provided for new drug research and development and innovative therapy.

Description

technical field [0001] The invention relates to heme oxygenase-1 inhibitor zinc protoporphyrin (Zinc protoporphyrin, ZnPP), which can significantly reduce cardiotoxicity caused by doxorubicin when used in combination with antitumor drug doxorubicin. Background technique [0002] Doxorubicin (DOX) belongs to anthracycline antitumor antibiotics. It has the characteristics of broad antitumor spectrum, strong antitumor effect and definite curative effect. It is widely used in the treatment of hematological malignancies and solid tumors, such as acute leukemia, lymph cancer, breast cancer, gastric cancer, soft tissue sarcoma and ovarian cancer. Similar to other antineoplastic drugs, doxorubicin has a strong damaging effect on cancerous cells on the one hand, and is also toxic to normal cells and tissues on the other hand, which can cause toxic side effects such as hair loss, bone marrow suppression, and cardiotoxicity. Among them, the biggest side effect of doxorubicin is irreve...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): A61K31/555A61P9/00
CPCA61K31/555
Inventor 王福俤方学贤韩丹王浩闵军霞
Owner ZHEJIANG UNIV
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