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用于肿瘤靶向的自供氧酶纳米凝胶,具有增强的协同饥饿和光动力疗法。

Oxygen self-supplied enzyme nanogels for tumor targeting with amplified synergistic starvation and photodynamic therapy.

作者信息

Fan Xiaotong, Luo Zheng, Chen Ying, Yeo Jayven Chee Chuan, Li Zibiao, Wu Yun-Long, He Chaobin

机构信息

Department of Materials Science and Engineering, National University of Singapore, 9 Engineering Drive 1, Singapore 117576, Singapore.

Fujian Provincial Key Laboratory of Innovative Drug Target Research and State Key Laboratory of Cellular Stress Biology, School of Pharmaceutical Sciences, Xiamen University, Xiamen, China.

出版信息

Acta Biomater. 2022 Apr 1;142:274-283. doi: 10.1016/j.actbio.2022.01.056. Epub 2022 Jan 31.

Abstract

Tumor tissues need vast supply of nutrients and energy to sustain the rapid proliferation of cancer cells. Cutting off the glucose supply represents a promising cancer therapy approach. Herein, a tumor tissue-targeted enzyme nanogel (rGCP nanogel) with self-supply oxygen capability was developed. The enzyme nanogel synergistically enhanced starvation therapy and photodynamic therapy (PDT) to mitigate the rapid proliferation of cancer cells. The rGCP nanogel was fabricated by copolymerizing two monomers, porphyrin and cancer cells-targeted, Arg-Gly-Asp (RGD), onto the glucose oxidase (GOX) and catalase (CAT) surfaces. The cascade reaction within the rGCP nanogel could efficiently consume intracellular glucose catalyzed by GOX. Concurrently, CAT safely decomposed the produced HO with systemic toxicity to promote oxygen generation and achieved low toxicity starvation therapy. The produced oxygen subsequently facilitated the glucose oxidation reaction and significantly enhanced the generation of cytotoxic singlet oxygen (O) in the presence of 660 nm light irradiation. Combining starvation therapy and PDT, the designed enzyme nanogel system presented an amplified synergic cancer therapy effect. This approach potentially paved a new way to fabricate a combinatorial therapy approach by employing cascaded catalytic nanomedicines with good tumor selectivity and efficient anti-cancer effect. STATEMENT OF SIGNIFICANCE: The performance of starvation and photodynamic therapy (PDT) is usually suppressed by intrinsic tumorous hypoxia. Herein, an oxygen self-supplied and tumor tissue-targeted enzyme nanogel was created by copolymerization of two monomers, porphyrin and cancer cell-targeted Arg-Gly-Asp (RGD), onto the surface of glucose oxidase (GOX) and catalase (CAT), which synergistically enhanced starvation therapy and PDT. Moreover, the enzyme nanogels possessed high stability and could be synthesized straightforwardly. This anti-cancer system provides an approach for constructing a combinatorial therapy approach by employing cascaded catalytic nanomedicine with good tumor selectivity and therapeutic efficacy.

摘要

肿瘤组织需要大量的营养和能量供应来维持癌细胞的快速增殖。切断葡萄糖供应是一种很有前景的癌症治疗方法。在此,开发了一种具有自供应氧气能力的肿瘤组织靶向酶纳米凝胶(rGCP纳米凝胶)。该酶纳米凝胶协同增强饥饿疗法和光动力疗法(PDT),以减轻癌细胞的快速增殖。rGCP纳米凝胶是通过将两种单体,卟啉和癌细胞靶向的精氨酸-甘氨酸-天冬氨酸(RGD),共聚到葡萄糖氧化酶(GOX)和过氧化氢酶(CAT)表面而制备的。rGCP纳米凝胶内的级联反应可以有效地消耗由GOX催化的细胞内葡萄糖。同时,CAT安全地分解产生的具有全身毒性的H₂O₂以促进氧气生成,并实现低毒性饥饿疗法。随后产生的氧气促进葡萄糖氧化反应,并在660nm光照射下显著增强细胞毒性单线态氧(¹O₂)的产生。结合饥饿疗法和PDT,所设计的酶纳米凝胶系统呈现出放大的协同癌症治疗效果。这种方法可能为通过采用具有良好肿瘤选择性和高效抗癌效果的级联催化纳米药物来制造联合治疗方法铺平一条新途径。意义声明:饥饿和光动力疗法(PDT)的性能通常受到肿瘤内源性缺氧的抑制。在此,通过将两种单体,卟啉和癌细胞靶向的精氨酸-甘氨酸-天冬氨酸(RGD),共聚到葡萄糖氧化酶(GOX)和过氧化氢酶(CAT)表面,创建了一种氧气自供应且肿瘤组织靶向的酶纳米凝胶,其协同增强了饥饿疗法和PDT。此外,该酶纳米凝胶具有高稳定性并且可以直接合成。这种抗癌系统提供了一种通过采用具有良好肿瘤选择性和治疗效果的级联催化纳米药物来构建联合治疗方法的途径。

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