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谷胱甘肽响应型多功能“特洛伊木马”纳米凝胶作为一种联合化疗和光动力抗癌治疗的纳米治疗一体化平台。

Glutathione-Responsive Multifunctional "Trojan Horse" Nanogel as a Nanotheranostic for Combined Chemotherapy and Photodynamic Anticancer Therapy.

机构信息

School of Materials and Energy & Chongqing Engineering Research Center for Micro-Nano Biomedical Materials and Devices, Southwest University, Chongqing 400715, P. R. China.

出版信息

ACS Appl Mater Interfaces. 2020 Nov 11;12(45):50896-50908. doi: 10.1021/acsami.0c15781. Epub 2020 Oct 27.

DOI:10.1021/acsami.0c15781
PMID:33107728
Abstract

It remains a great challenge to design a multifunctional and robust nanoplatform for stimuli-responsive drug delivery toward a lesion, which tactfully integrates multiple molecules with therapeutic and diagnostic characteristics. Herein, we reported a facile and ingenious cross-linked nanogel (DSA) based on the chemical cross-link of drugs as a straightforward strategy to overcome the instability of the assembly. In DSA, doxorubicin (DOX) and 5-aminolevulinic acid (ALA) were cross-linked with a disulfide linker for realizing synergistic anticancer therapy. The stability of DSA was adjusted balancing the hydrophobic/hydrophilic property with hydrophilic NH-PEG. After regulating the coordination of the DOX part and ALA moiety, the drug-loaded nanogel exhibited superior chemotherapeutic efficacies. Additionally, the DSA could selectively biosynthesize fluorescent protoporphyrin IX (PpIX) in tumor cells, which could be applied for a real-time imaging probe of accurate cancer diagnosis. Besides, the synthesized PpIX in mitochondria could serve as a photosensitizer to convert oxygen into toxic reactive oxygen species under a near infrared ray at 660 nm irradiation, leading to an excellent tumor-killing efficacy. This work proposed a unique strategy for designing a series of prodrug nanogels as a universal drug delivery platform for realizing precise disease therapy and diagnostics.

摘要

设计用于刺激响应药物递送到病变部位的多功能和稳健纳米平台仍然是一个巨大的挑战,这需要巧妙地整合具有治疗和诊断特性的多种分子。在此,我们报道了一种基于药物化学交联的简便而巧妙的交联纳米凝胶(DSA),作为克服组装不稳定性的直接策略。在 DSA 中,阿霉素(DOX)和 5-氨基酮戊酸(ALA)通过二硫键连接子交联,以实现协同抗癌治疗。通过平衡疏水性/亲水性与亲水性 NH-PEG 来调整 DSA 的稳定性。调节 DOX 部分和 ALA 部分的配位后,载药纳米凝胶表现出优异的化疗效果。此外,DSA 可以在肿瘤细胞中选择性地生物合成荧光原卟啉 IX(PpIX),可作为实时成像探针用于准确癌症诊断。此外,合成的 PpIX 在线粒体中可作为光敏剂,在 660nm 近红外光照射下将氧气转化为有毒的活性氧,从而具有优异的肿瘤杀伤效果。这项工作提出了一种独特的策略,用于设计一系列前药纳米凝胶作为通用药物递送平台,以实现精确的疾病治疗和诊断。

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