A pharmaceutical composition of peridinin and doxorubicin and application thereof

By combining doxorubicin with doxorubicin, the problem of multidrug resistance in the treatment of breast cancer with doxorubicin was solved, achieving significant inhibition of the proliferation of doxorubicin-resistant cells and excellent tumor-suppressing effects, while maintaining good safety.

CN122398831APending Publication Date: 2026-07-17EAST CHINA UNIV OF SCI & TECH

Patent Information

Authority / Receiving Office
CN · China
Patent Type
Applications(China)
Current Assignee / Owner
EAST CHINA UNIV OF SCI & TECH
Filing Date
2026-04-28
Publication Date
2026-07-17

AI Technical Summary

Technical Problem

Doxorubicin is prone to multidrug resistance when treating breast cancer, especially for some subtypes (such as ER+), and there is a lack of effective treatment options to reverse resistance.

Method used

A pharmaceutical composition is prepared by combining daunoflavin and doxorubicin in a preferred molar ratio of 6.5:1 to 27.2:1, including pharmaceutically acceptable excipients, and in the form of an injection, tablet, capsule or topical dosage form for the treatment of breast cancer.

Benefits of technology

In vitro experiments showed that the combination of doxydin and doxorubicin significantly inhibited the proliferation of doxorubicin-resistant cells compared to doxorubicin alone. In vivo experiments demonstrated excellent tumor-suppressing effects with no significant systemic toxicity and good safety profile.

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Abstract

本发明公开了一种药物组合物,包括多甲藻黄素和多柔比星。本发明还公开了如上所述的药物组合物在制备治疗乳腺癌的药物中的应用。本发明首次发现并证实了多甲藻黄素与多柔比星在对抗乳腺癌多柔比星耐药株(MCF‑7 / ADR)上具有明确的协同作用。在动物模型中,本发明的组合物表现出优异的剂量依赖性抑瘤效果。与单用多柔比星相比,高剂量组合物(25μM多甲藻黄素+500 ng / mL多柔比星)治疗27天后,能使肿瘤体积减少36.21%。在整个给药周期内,各剂量组合物治疗组的小鼠体重与对照组相比均无显著下降,表明该组合物在发挥显著体内药效的同时,未增加可观测的全身毒性,具备临床转化潜力。
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