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天然装备的尿液外泌体包被聚(2-乙基-2-恶唑啉)-聚(D,L-丙交酯)纳米载体用于乳腺癌的临床前转化

Naturally Equipped Urinary Exosomes Coated Poly (2-ethyl-2-oxazoline)-Poly (D, L-lactide) Nanocarriers for the Pre-Clinical Translation of Breast Cancer.

作者信息

Ni Jiang, Mi Yuanyuan, Wang Bei, Zhu Yuting, Ding Yang, Ding Yongjuan, Li Xia

机构信息

Department of Pharmacy, Affiliated Hospital of Jiangnan University, Wuxi 214000, China.

College of Pharmacy, Pharmaceutical Series, China Pharmaceutical University, Nanjing 210000, China.

出版信息

Bioengineering (Basel). 2022 Aug 3;9(8):363. doi: 10.3390/bioengineering9080363.

Abstract

Recently, biomimetic nanoparticles for tumor-targeted therapy have attracted intensifying interest. Although exosomes are an excellent biomimetic material, numerous challenges are still hindering its clinical applications, such as low yield, insufficient targeting efficiency, and high cost. In this work, urinary exosomes (UEs) with high expression of CD9 and CD47 were extracted from breast cancer patients by a non-invasive method. Here, a nanotechnology approach is reported for tumor homologous targeting via CD9 and phagocytosis escape via CD47 through UE-coated poly (2-ethyl-2-oxazoline)-poly (D, L-lactide) (PEOz-PLA) nanoparticles (UEPP NPs). The cytotoxic agent doxorubicin (DOX)-loaded UEPP (UEPP-D) NPs with an initial particle size of 61.5 nm showed a burst release under acidic condition mimicking the tumor microenvironment. In vitro experiments revealed that UEPP-D NPs exhibited significantly improved cellular uptake, cytotoxicity, and apoptosis in MCF-7 cell lines as compared to DOX-loaded PEOz-PLA nanoparticles (PP-D NPs) and free DOX. More importantly, anti-phagocytosis and pharmacokinetic studies confirmed that UEPP-D NPs had superior immune escape ability and significantly prolonged the drug's bloodstream circulation in vivo. Finally, UEPP-D NPs showed a markedly higher antitumor efficacy and lower side-toxicity in MCF-7 tumor bearing nude mice model. Thus, this versatile nano-system with immune escape, homologous targeting, and rapid response release characteristics could be a promising tool for breast cancer treatment.

摘要

近年来,用于肿瘤靶向治疗的仿生纳米颗粒引起了越来越多的关注。尽管外泌体是一种出色的仿生材料,但仍有许多挑战阻碍其临床应用,例如产量低、靶向效率不足和成本高。在这项工作中,通过非侵入性方法从乳腺癌患者中提取了高表达CD9和CD47的尿液外泌体(UEs)。在此,报道了一种纳米技术方法,即通过包被UE的聚(2-乙基-2-恶唑啉)-聚(D,L-丙交酯)(PEOz-PLA)纳米颗粒(UEPP NPs)实现通过CD9进行肿瘤同源靶向以及通过CD47实现吞噬逃逸。负载细胞毒性药物阿霉素(DOX)的UEPP(UEPP-D)NPs初始粒径为61.5 nm,在模拟肿瘤微环境的酸性条件下表现出突释。体外实验表明,与负载DOX的PEOz-PLA纳米颗粒(PP-D NPs)和游离DOX相比,UEPP-D NPs在MCF-7细胞系中表现出显著改善的细胞摄取、细胞毒性和细胞凋亡。更重要的是,抗吞噬和药代动力学研究证实,UEPP-D NPs具有优异的免疫逃逸能力,并在体内显著延长了药物的血液循环时间。最后,UEPP-D NPs在荷MCF-7肿瘤的裸鼠模型中显示出明显更高的抗肿瘤疗效和更低的副作用。因此,这种具有免疫逃逸、同源靶向和快速响应释放特性的多功能纳米系统可能是一种有前途的乳腺癌治疗工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af89/9404723/72271ed568d9/bioengineering-09-00363-sch001.jpg

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