Key Laboratory of Biomaterials of Guangdong Higher Education Institutes, Department of Biomedical Engineering, Jinan University, Guangzhou 510632, China.
Department of Orthopedics, The First Affiliated Hospital of Jinan University, Guangzhou 510632, China.
Theranostics. 2020 May 15;10(14):6245-6260. doi: 10.7150/thno.45456. eCollection 2020.
Although the enzyme catalytic nanoreactors reported so far have achieved excellent therapeutic efficacy, how to accurately exert enzyme activity in the tumor microenvironment to specifically kill tumor cells and avoid systemic oxidative damage would be an inevitable challenge for catalytic nanomedicine. At the present study, we fabricate an advanced biomimetic nanoreactor, SOD-Fe@Lapa-ZRF for tumor multi-enzyme cascade delivery that combined specifically killing tumor cells and protect cells from oxidative stress. : We first synthesized the FeNP-embedded SOD (SOD-Fe) by reduction reaction using sodium borohydride. Next, SOD-Fe and Lapa cargo were encapsulated in ZIF-8 by self-assembly. In order to protect the cargo enzyme from digestion by protease and prolong blood circulating time, SOD-Fe@Lapa-Z was further cloaked with RBC membrane and functionalized with folate targeting, resulting in the final advanced biomimetic nanoreactor SOD-Fe@Lapa-ZRF. : Once internalized, ZIF-8 achieves pH-triggered disassembly in weakly acidic tumor microenvironment. The released SOD-Fe and Lapa were further endocytosed by tumor cells and the Lapa produces superoxide anion (O) through the catalysis of NQO1 that is overexpressed in tumor cells, while O is converted to HO via SOD. At this time, the released ferrous ions from SOD-Fe and HO are further transformed to highly toxic hydroxyl radicals (•OH) for specifically killing tumor cells, and there was no obvious toxicological response during long-term treatment. Importantly, SOD-Fe@Lapa-ZRF enhanced the normal cell's anti-oxidation ability, and thus had little effect on the secretion of TNF-α, IL-6 and IL-1β pro-inflammatory cytokines, while effectively reversed the decreased activity of T-SOD and GSH-Px and remained stable MDA content after tumor treatment. and results indicate that the tumor microenvironment-responsive release multi-enzyme cascade have high tumor specificity and effective anti-tumor efficacy, and can protect cells from oxidative stress damage. : The biomimetic nanoreactor will have a great potential in cancer nanomedicine and provide a novel strategy to regulate oxidative stress.
虽然迄今为止报道的酶催化纳米反应器已经取得了优异的治疗效果,但如何在肿瘤微环境中准确发挥酶活性,特异性杀死肿瘤细胞并避免全身氧化损伤,将是催化纳米医学不可避免的挑战。在本研究中,我们构建了一种先进的仿生纳米反应器 SOD-Fe@Lapa-ZRF,用于肿瘤多酶级联递药,既能特异性杀伤肿瘤细胞,又能保护细胞免受氧化应激损伤。我们首先通过使用硼氢化钠的还原反应合成了 FeNP 嵌入的 SOD(SOD-Fe)。接下来,SOD-Fe 和 Lapa 货物通过自组装封装在 ZIF-8 中。为了保护货物酶免受蛋白酶的消化并延长血液循环时间,SOD-Fe@Lapa-Z 进一步被红细胞膜包裹,并通过叶酸靶向功能化,得到最终的先进仿生纳米反应器 SOD-Fe@Lapa-ZRF。一旦被内化,ZIF-8 在弱酸性肿瘤微环境中实现 pH 触发的解体。释放的 SOD-Fe 和 Lapa 被肿瘤细胞进一步内吞,Lapa 通过在肿瘤细胞中过度表达的 NQO1 催化产生超氧阴离子(O),而 O 通过 SOD 转化为 HO。此时,SOD-Fe 释放的亚铁离子和 HO 进一步转化为高毒性羟基自由基(•OH),特异性杀伤肿瘤细胞,长期治疗过程中无明显毒理学反应。重要的是,SOD-Fe@Lapa-ZRF 增强了正常细胞的抗氧化能力,因此对 TNF-α、IL-6 和 IL-1β 促炎细胞因子的分泌影响不大,而有效地逆转了 T-SOD 和 GSH-Px 活性的降低,并在肿瘤治疗后保持稳定的 MDA 含量。结果表明,肿瘤微环境响应性释放多酶级联具有高肿瘤特异性和有效的抗肿瘤疗效,并能保护细胞免受氧化应激损伤。仿生纳米反应器在癌症纳米医学中有很大的应用潜力,为调节氧化应激提供了一种新的策略。