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可生物降解的锰掺杂磷酸钙纳米诊疗一体化用于可追踪级联反应增强抗肿瘤治疗

Biodegradable Manganese-Doped Calcium Phosphate Nanotheranostics for Traceable Cascade Reaction-Enhanced Anti-Tumor Therapy.

机构信息

Marshall Laboratory of Biomedical Engineering, International Cancer Center, Laboratory of Evolutionary Theranostics (LET), School of Biomedical Engineering, Health Science Center , Shenzhen University , Shenzhen 518060 , China.

Key Laboratory of Optoelectronic Devices and Systems of Ministry of Education and Guangdong Province, College of Optoelectronic Engineering , Shenzhen University , Shenzhen 518060 , China.

出版信息

ACS Nano. 2019 Dec 24;13(12):13985-13994. doi: 10.1021/acsnano.9b05836. Epub 2019 Dec 13.

Abstract

Glucose oxidase (GOx) has been recognized as a "star" enzyme catalyst involved in cancer treatment in the past few years. Herein, GOx is mineralized with manganese-doped calcium phosphate (MnCaP) to form spherical nanoparticles (GOx-MnCaP NPs) by an biomimetic mineralization method, followed by the loading of doxorubicin (DOX) to construct a biodegradable, biocompatible, and tumor acidity-responsive nanotheranostics for magnetic resonance imaging (MRI) and cascade reaction-enhanced cooperative cancer treatment. The GOx-driven oxidation reaction can effectively eliminate intratumoral glucose for starvation therapy, and the elevated HO is then converted into highly toxic hydroxyl radicals a Mn-mediated Fenton-like reaction for chemodynamic therapy (CDT). Moreover, the acidity amplification due to the gluconic acid generation will in turn accelerate the degradation of the nanoplatform and promote the Mn-HO reaction for enhanced CDT. Meanwhile, the released Mn ions can be used for MRI to monitor the treatment process. After carrying the anticancer drug, the DOX-loaded GOx-MnCaP can integrate starvation therapy, Mn-mediated CDT, and DOX-induced chemotherapy together, which showed greatly improved therapeutic efficacy than each monotherapy. Such an orchestrated cooperative cancer therapy demonstrated high-efficiency tumor suppression on 4T1 tumor-bearing mice with minimal side effects. Our findings suggested that the DOX-loaded GOx-MnCaP nanotheranostics with excellent biodegradability and biocompatibility hold clinical translation potential for cancer management.

摘要

葡萄糖氧化酶(GOx)在过去几年中被认为是一种参与癌症治疗的“明星”酶催化剂。在此,通过仿生矿化方法将 GOx 与掺锰磷酸钙(MnCaP)矿化,形成球形纳米颗粒(GOx-MnCaP NPs),然后负载阿霉素(DOX)构建可生物降解、生物相容且对肿瘤酸度有响应的磁共 振成像(MRI)和级联反应增强协同癌症治疗的纳米诊疗剂。GOx 驱动的氧化反应可有效消除肿瘤内葡萄糖进行饥饿治疗,升高的 HO 随后转化为高度毒性的羟基自由基,通过 Mn 介导的芬顿样反应进行化学动力学治疗(CDT)。此外,由于葡萄糖酸的生成导致的酸度放大反过来又会加速纳米平台的降解,并促进 Mn-HO 反应以增强 CDT。同时,释放的 Mn 离子可用于 MRI 监测治疗过程。载药后,负载 DOX 的 GOx-MnCaP 可将饥饿治疗、Mn 介导的 CDT 和 DOX 诱导的化疗结合在一起,与每种单一疗法相比,其治疗效果大大提高。这种协调的协同癌症治疗在 4T1 荷瘤小鼠上表现出高效的肿瘤抑制作用,副作用极小。我们的研究结果表明,具有优异的生物降解性和生物相容性的负载 DOX 的 GOx-MnCaP 纳米诊疗剂具有癌症管理的临床转化潜力。

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