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用于协同缓解缺氧以增强线粒体靶向光动力治疗的氧气罐。

Oxygen tank for synergistic hypoxia relief to enhance mitochondria-targeted photodynamic therapy.

作者信息

Li Xianghui, Wang Haoran, Li Zhiyan, Li Dandan, Lu Xiaofeng, Ai Shichao, Dong Yuxiang, Liu Song, Wu Jinhui, Guan Wenxian

机构信息

Department of Gastrointestinal Surgery, Affiliated Nanjing Drum Tower Hospital, Nanjing University Medical School, Nanjing, 210008, China.

State Key Laboratory of Pharmaceutical Biotechnology, Medical School and School of Life Science, Nanjing University, Nanjing, 210093, China.

出版信息

Biomater Res. 2022 Sep 22;26(1):47. doi: 10.1186/s40824-022-00296-0.

Abstract

BACKGROUND

Mitochondria play an essential role in cellular redox homeostasis maintenance and meanwhile serve as an important target for organelle targeted therapy. Photodynamic therapy (PDT) is a promising strategy for organelle targeted therapy with noninvasive nature and highly spatiotemporal selectivity. However, the efficacy of PDT is not fully achieved due to tumor hypoxia. Moreover, aerobic respiration constantly consumes oxygen and leads to a lower oxygen concentration in mitochondria, which continuously limited the therapeutic effects of PDT. The lack of organelle specific oxygen delivery method remains a main challenge.

METHODS

Herein, an Oxygen Tank is developed to achieve the organelle targeted synergistic hypoxia reversal strategy, which not only act as an oxygen storage tank to open sources and reduce expenditure, but also coated with red blood cell membrane like the tank with stealth coating. Within the oxygen tank, a mitochondrion targeted photosensitizer (IR780) and a mitochondria respiration inhibitor (atovaquone, ATO) are co-loaded in the RBC membrane (RBCm) coated perfluorocarbon (PFC) liposome core.

RESULTS

Inside these bio-mimic nanoparticles, ATO effectively inhibits mitochondrial respiration and economized endogenous oxygen consumption, while PFC supplied high-capacity exogenous oxygen. These Oxygen modulators reverse the hypoxia status in vitro and in vivo, and exhibited a superior anti-tumor activity by mitochondria targeted PDT via IR780. Ultimately, the anti-tumor effects towards gastric cancer and colon cancer are elicited in vivo.

CONCLUSIONS

This oxygen tank both increases exogeneous oxygen supply and decreases endogenous oxygen consumption, may offer a novel solution for organelle targeted therapies.

摘要

背景

线粒体在维持细胞氧化还原稳态中起着至关重要的作用,同时也是细胞器靶向治疗的重要靶点。光动力疗法(PDT)是一种具有非侵入性和高度时空选择性的细胞器靶向治疗的有前景的策略。然而,由于肿瘤缺氧,PDT的疗效尚未完全实现。此外,有氧呼吸不断消耗氧气,导致线粒体中的氧浓度降低,这不断限制了PDT的治疗效果。缺乏细胞器特异性氧输送方法仍然是一个主要挑战。

方法

在此,开发了一种氧罐以实现细胞器靶向协同缺氧逆转策略,它不仅作为一个氧储存罐开源节流,还像带有隐形涂层的罐子一样包裹着红细胞膜。在氧罐内部,一种线粒体靶向光敏剂(IR780)和一种线粒体呼吸抑制剂(阿托伐醌,ATO)共同负载在红细胞膜(RBCm)包被的全氟化碳(PFC)脂质体核心中。

结果

在这些仿生纳米颗粒内部,ATO有效抑制线粒体呼吸并节约内源性氧消耗,而PFC提供高容量的外源性氧。这些氧调节剂在体外和体内逆转缺氧状态,并通过IR780介导的线粒体靶向PDT表现出优异的抗肿瘤活性。最终,在体内引发了对胃癌和结肠癌的抗肿瘤作用。

结论

这种氧罐既增加外源性氧供应又减少内源性氧消耗,可能为细胞器靶向治疗提供一种新的解决方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d4f/9502906/6faa3ba7b407/40824_2022_296_Sch1_HTML.jpg

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