Use of amifostine combined with ursolic acid in the preparation of a preparation for preventing and / or treating radiation-induced lung injury

The combined use of amifostine and ursolic acid overcomes the limitations of single-mechanism drugs in the prevention and treatment of radiation-induced lung injury in existing technologies, achieving multi-stage and multi-target protection against radiation-induced lung injury, significantly reducing lung tissue damage, and showing good prospects for clinical translation.

CN122398820APending Publication Date: 2026-07-17XINXIANG MEDICAL UNIV
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Patent Information

Authority / Receiving Office
CN · China
Patent Type
Applications(China)
Current Assignee / Owner
XINXIANG MEDICAL UNIV
Filing Date
2026-06-03
Publication Date
2026-07-17

AI Technical Summary

Technical Problem

There is a lack of highly effective, low-toxicity drugs that can intervene in multiple aspects of radiation-induced lung injury in the current technology. Amifostine has a short half-life and large side effects in clinical applications, while ursolic acid has poor water solubility and low bioavailability. Research on its use alone or in combination for radiation-induced lung injury is still not systematic.

Method used

Amifostine and ursolic acid can be used in combination to form single or independent formulations that cover multiple stages of radiation-induced lung injury through different mechanisms. Amifostine focuses on the early clearance of free radicals during radiotherapy, while ursolic acid continuously intervenes in the inflammatory response and fibrosis process. These formulations can be prepared for oral, injection, inhalation, or transdermal administration.

Benefits of technology

It significantly eliminates X-ray-induced reactive oxygen species, protects cells from radiation damage, reduces lung fibrosis scores, reduces systemic adverse reactions, overcomes the bioavailability deficiency of ursolic acid, and provides the advantages of multi-target and multi-stage comprehensive intervention.

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Abstract

本发明涉及生物医药技术领域,尤其涉及氨磷汀联合熊果酸在制备预防和 / 或治疗放射性肺损伤的制剂中的应用。本发明提供的联合用药方案覆盖了放射性肺损伤从急性氧化应激、细胞增殖抑制到慢性纤维化形成的多个病理环节,具有多靶点、多阶段的综合干预优势。通过联合应用,有望降低各自有效剂量,从而减少氨磷汀的系统性不良反应并克服熊果酸生物利用度低的缺陷。该组合具有良好的制剂适应性和临床转化前景,为放射性肺损伤的防治提供了新的有效策略。
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