Dual-pore protocells with multitasking capacities for simultaneous delivery of therapeutic enzymes and drugs in macrophage depletion therapy†

IF 5.7 3区 医学 Q1 MATERIALS SCIENCE, BIOMATERIALS
Jorge Parra-Nieto, Alicia Arroyo-Nogales, Diana Marcos-Fernández, Sandra Jimenez-Falcao, Carmen Arribas, Diego Megias, África Gonzalez-Murillo, Manuel Ramirez and Alejandro Baeza
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引用次数: 0

Abstract

Macrophages are usually present in solid tumors where they participate in tumor progression, angiogenesis, immunosuppression and metastasis. The design of nanocarriers capable of delivering therapeutic agents to specific cell populations has received considerable attention in the last decades. However, the capacity of many of these nanosystems to deliver multiple therapeutic agents with very different chemical properties is more limited. Herein, a novel multitasking nanoplatform capable of delivering large macromolecules and cytotoxic drugs to macrophages is presented. This novel nanosystem has exhibited excellent skills in performing simultaneous tasks, macrophage depletion and glucose starvation, maintaining the oxygen levels in the tissue. This nanodevice is composed of a dual-pore mesoporous silica core with the capacity to house small cytotoxic drugs, such as doxorubicin or zoledronic acid, and large macromolecules, such as glucose oxidase. The external surface of the silica core was coated with a lipid bilayer to avoid the premature release of the housed drugs. Finally, polymeric nanocapsules loaded with catalase were covalently anchored on the outer lipid bilayer, and carboxy-mannose was attached to the exposed side of the nanocapsules to provide selectivity to the macrophages. These nanoassemblies were able to transport enzymes (Gox and CAT), maintaining their catalytic activity. Therefore, they could induce glucose starvation, keeping the oxygen levels in the tissue, owing to the tandem enzymatic reaction. The capacity of these nanoassemblies to deliver therapeutic agents to macrophages was evaluated both in static and under flow conditions, showing a rapid capture of the nanoparticles by the macrophages. Once there, the nanoassemblies also exhibited excellent capacity to induce potent macrophage depletion. This strategy can be directly adapted for the treatment of different malignancies due to the modular nature of the nanoplatform, which can be loaded with different therapeutic agent combinations and pave the way for the development of personalized nanomedicines for diverse types of tumors.

Abstract Image

Abstract Image

具有多任务处理能力的双孔原细胞,可在巨噬细胞耗竭疗法中同时输送治疗酶和药物
巨噬细胞通常存在于实体瘤中,参与肿瘤进展、血管生成、免疫抑制和转移。过去几十年来,能够向特定细胞群递送治疗药物的纳米载体的设计受到了广泛关注。然而,许多此类纳米系统在递送化学性质迥异的多种治疗剂方面的能力较为有限。本文介绍了一种新型多任务纳米平台,它能够向巨噬细胞输送大分子和细胞毒性药物。这种新型纳米系统在同时执行巨噬细胞耗竭和葡萄糖饥饿任务、维持组织内氧气水平方面表现出卓越的技能。这种纳米器件由双孔介孔二氧化硅内核组成,可容纳多柔比星或唑来膦酸等小细胞毒性药物和葡萄糖氧化酶等大分子。二氧化硅核心的外表面涂有一层脂质双分子层,以避免所容纳的药物过早释放。最后,负载有过氧化氢酶的聚合物纳米胶囊被共价锚定在外部脂质双分子层上,羧基甘露糖被附着在纳米胶囊的暴露面上,以提供对巨噬细胞的选择性。这些纳米组件能够运输酶(Gox 和 CAT),并保持其催化活性。因此,由于串联酶反应,它们可以诱导葡萄糖饥饿,保持组织中的氧含量。在静态和流动条件下对这些纳米组合体向巨噬细胞输送治疗药物的能力进行了评估,结果表明巨噬细胞能迅速捕获纳米粒子。一旦被巨噬细胞捕获,这些纳米组合物还表现出诱导巨噬细胞有效消耗的卓越能力。由于纳米平台的模块化特性,这种策略可以直接用于治疗不同的恶性肿瘤,它可以装载不同的治疗剂组合,为开发治疗各种类型肿瘤的个性化纳米药物铺平了道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Biomaterials Science
Biomaterials Science MATERIALS SCIENCE, BIOMATERIALS-
CiteScore
11.50
自引率
4.50%
发文量
556
期刊介绍: Biomaterials Science is an international high impact journal exploring the science of biomaterials and their translation towards clinical use. Its scope encompasses new concepts in biomaterials design, studies into the interaction of biomaterials with the body, and the use of materials to answer fundamental biological questions.
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