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通过间隔基设计化学实现具有肿瘤特异性化疗递送功能的活性氧(ROS)响应性聚合物囊泡

Reactive Oxygen Species (ROS)-Responsive Polymersomes with Site-Specific Chemotherapeutic Delivery into Tumors via Spacer Design Chemistry.

作者信息

Jäger Eliézer, Sincari Vladimir, Albuquerque Lindomar J C, Jäger Alessandro, Humajova Jana, Kucka Jan, Pankrac Jan, Paral Petr, Heizer Tomas, Janouskova Olga, Konefał Rafał, Pavlova Ewa, Sedlacek Ondrej, Giacomelli Fernando C, Pouckova Pavla, Sefc Ludek, Stepanek Petr, Hruby Martin

机构信息

Institute of Macromolecular Chemistry, Heyrovsky Sq. 2, 162 06 Prague, Czech Republic.

Centro de Ciências Naturais e Humanas, Universidade Federal do ABC, Avenida dos Estados 5001, Santo André 09210-580, Brazil.

出版信息

Biomacromolecules. 2020 Apr 13;21(4):1437-1449. doi: 10.1021/acs.biomac.9b01748. Epub 2020 Mar 4.

Abstract

The lack of cellular and tissue specificities in conventional chemotherapies along with the generation of a complex tumor microenvironment (TME) limits the dosage of active agents that reaches tumor sites, thereby resulting in ineffective responses and side effects. Therefore, the development of selective TME-responsive nanomedicines is of due relevance toward successful chemotherapies, albeit challenging. In this framework, we have synthesized novel, ready-to-use ROS-responsive amphiphilic block copolymers (BCs) with two different spacer chemistry designs to connect a hydrophobic boronic ester-based ROS sensor to the polymer backbone. Hydrodynamic flow focusing nanoprecipitation microfluidics (MF) was used in the preparation of well-defined ROS-responsive PSs; these were further characterized by a combination of techniques [H NMR, dynamic light scattering (DLS), static light scattering (SLS), transmission electron microscopy (TEM), and cryogenic TEM (cryo-TEM)]. The reaction with hydrogen peroxide releases an amphiphilic phenol or a hydrophilic carboxylic acid, which affects polymersome (PS) stability and cargo release. Therefore, the importance of the spacer chemistry in BC deprotection and PS stability and cargo release is herein highlighted. We have also evaluated the impact of spacer chemistry on the PS-specific release of the chemotherapeutic drug doxorubicin (DOX) into tumors in vitro and in vivo. We demonstrate that by spacer chemistry design one can enhance the efficacy of DOX treatments (decrease in tumor growth and prolonged animal survival) in mice bearing EL4 T cell lymphoma. Side effects (weight loss and cardiotoxicity) were also reduced compared to free DOX administration, highlighting the potential of the well-defined ROS-responsive PSs as TME-selective nanomedicines. The PSs could also find applications in other environments with high ROS levels, such as chronic inflammations, aging, diabetes, cardiovascular diseases, and obesity.

摘要

传统化疗缺乏细胞和组织特异性,同时复杂肿瘤微环境(TME)的形成限制了到达肿瘤部位的活性剂剂量,从而导致治疗效果不佳和副作用。因此,开发选择性TME响应纳米药物对于成功的化疗至关重要,尽管具有挑战性。在此框架下,我们合成了新型的、即用型的ROS响应两亲性嵌段共聚物(BCs),采用两种不同的间隔基化学设计将基于硼酸酯的疏水性ROS传感器连接到聚合物主链上。利用流体动力聚焦纳米沉淀微流控技术(MF)制备了定义明确的ROS响应聚合物囊泡(PSs);通过多种技术[核磁共振氢谱(1H NMR)、动态光散射(DLS)、静态光散射(SLS)、透射电子显微镜(TEM)和低温透射电子显微镜(cryo-TEM)]对其进行了进一步表征。与过氧化氢的反应会释放出两亲性苯酚或亲水性羧酸,这会影响聚合物囊泡(PS)的稳定性和药物释放。因此,本文强调了间隔基化学在BC脱保护以及PS稳定性和药物释放中的重要性。我们还评估了间隔基化学对化疗药物阿霉素(DOX)在体外和体内向肿瘤部位特异性释放的影响。我们证明,通过间隔基化学设计,可以提高携带EL4 T细胞淋巴瘤的小鼠中DOX治疗的疗效(肿瘤生长减缓,动物存活时间延长)。与游离DOX给药相比,副作用(体重减轻和心脏毒性)也有所降低,突出了定义明确的ROS响应PSs作为TME选择性纳米药物的潜力。这些PSs还可应用于其他具有高ROS水平的环境,如慢性炎症、衰老、糖尿病、心血管疾病和肥胖症。

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