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微环境响应型靶向纳米医学用于协同肿瘤治疗与骨缺损修复

Microenvironment-Responsive Targeted Nanomedicine for a Collaborative Integration of Tumor Theranostics and Bone Defect Repair.

机构信息

Laboratory of Molecular Imaging, Fifth Hospital of Shanxi Medical University (Shanxi Provincial People's Hospital), Taiyuan, 030000, China.

Department of Orthopedics, Third Hospital of Shanxi Medical University, Shanxi Bethune Hospital, Shanxi Academy of Medical Sciences, Tongji Shanxi Hospital, Taiyuan, 030032, China.

出版信息

Adv Healthc Mater. 2024 Oct;13(27):e2400715. doi: 10.1002/adhm.202400715. Epub 2024 Jun 8.

Abstract

Despite advancements in breast cancer treatment, bone metastases remain a significant concern for advanced breast cancer patients. Current theranostics strategies face challenges in integrating tumor theranostics and bone formation. Herein, this work develops an activatable targeted nanomedicine AuMnCO@BSA-N (AMCBN) to enable a novel collaborative integration of second near-infrared (NIR-II) fluorescence imaging guided precise theranostics for breast cancer bone metastases and osteogenic microenvironment remolding. This strategy employs a chemical coordination between noble metal complex and metal carbonyl (MnCO), with surface modification of azide groups to enhance tumor affinity through passive and active targeting. The initiated respondent behavior of AMCBN by tumor microenvironment accelerate the degradation of coordinated MnCO, resulting in a rapid release of multifunctional agents for efficient chemodynamic therapy (CDT)/gas synergistic therapy. Meanwhile, the exceptional bone-binding properties enable the efficient and controlled release of Mn ions and carbon monoxide (CO) in the bone microenvironment, thereby facilitating the expression of osteogenesis-related proteins and establishing a novel synchronous theranostics process for tumor-bone repair.

摘要

尽管乳腺癌治疗取得了进展,但骨转移仍然是晚期乳腺癌患者的一个重大关注点。当前的治疗策略在整合肿瘤治疗和骨形成方面面临挑战。在此,本工作开发了一种可激活的靶向纳米药物 AuMnCO@BSA-N(AMCBN),以实现新型协同整合,用于乳腺癌骨转移的近红外二区(NIR-II)荧光成像引导精确治疗和成骨微环境重塑。该策略利用贵金属配合物与金属羰基化合物(MnCO)之间的化学配位,并通过叠氮基团的表面修饰,通过被动和主动靶向增强肿瘤亲和力。肿瘤微环境中 AMCBN 的起始响应行为加速了配位 MnCO 的降解,导致多功能试剂的快速释放,从而实现高效的化学动力学治疗(CDT)/气体协同治疗。同时,其出色的骨结合特性可在骨微环境中实现 Mn 离子和一氧化碳(CO)的高效和控制释放,从而促进成骨相关蛋白的表达,并建立一种用于肿瘤-骨修复的新型同步治疗过程。

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