A nano-delivery system based on dual synergistic tumor therapy

By constructing a metal-organic framework nanodelivery system that integrates chemiluminescent reagents, energy transfer materials, and the CRISPR-Cas9 gene editing system, the problems of limited tissue penetration depth and inhibition of the antioxidant system in tumor treatment were solved, achieving efficient and precise synergistic therapeutic effects.

CN122399052APending Publication Date: 2026-07-17HAINAN MEDICAL UNIV
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Patent Information

Authority / Receiving Office
CN · China
Patent Type
Applications(China)
Current Assignee / Owner
HAINAN MEDICAL UNIV
Filing Date
2026-04-23
Publication Date
2026-07-17

AI Technical Summary

Technical Problem

Among existing tumor treatment technologies, photodynamic therapy and chemodynamic therapy have problems such as limited tissue penetration depth and insufficient H2O2 concentration in the tumor microenvironment, and lack effective inhibition of the antioxidant system, resulting in poor treatment effects; graphene quantum dot diagnostic and treatment systems have limited functions and cannot achieve dynamic synergy between diagnosis and treatment.

Method used

A metal-organic framework-based nanodelivery system was constructed, integrating chemiluminescent reagents, energy transfer materials, and a CRISPR-Cas9 gene editing system. Utilizing the tumor microenvironment's responsive release and nuclear targeting capabilities, it achieves synergistic therapy through self-powered reactive oxygen species generation and gene editing.

Benefits of technology

It achieves enhanced efficacy in tumor treatment, breaks through the limitations of tissue penetration depth, significantly improves drug accumulation efficiency at the tumor site, reduces systemic toxicity, provides treatment effect assessment through real-time monitoring, and has good biocompatibility.

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Abstract

本发明属于生物医药与纳米材料技术领域,具体涉及一种基于双协同肿瘤治疗的纳米递送系统。本发明中该系统以肿瘤细胞核靶向碳量子点(GTTN)为核心功能介质,将化学发光试剂鲁米诺、CRISPR‑Cas9基因编辑系统封装于ZIF型金属有机框架载体,表面修饰透明质酸实现主动靶向。其通过肿瘤微环境内源性过氧化氢驱动鲁米诺化学发光,经化学共振能量转移激发GTTN产生活性氧,同时CRISPR‑Cas9系统敲除抗氧化基因,形成双协同治疗通路,兼具诊疗一体化功能。本发明解决了传统肿瘤治疗依赖外源光、靶向性差、易耐药的问题,抑瘤效果显著且生物相容性良好,具有重要临床转化价值。
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