Copper(II)-Complexed Polyethylenimine-Entrapped Gold Nanoparticles Enable Targeted CT/MR Imaging and Chemodynamic Therapy of Tumors.

IF 4.9 3区 工程技术 Q1 POLYMER SCIENCE Polymers Pub Date : 2025-02-06 DOI:10.3390/polym17030423
Lingxiu He, Na Liu, Risong Pan, Jingyi Zhu
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Abstract

Transition-metal ion copper(II) (Cu(II)) has drawn increasing attention as a small-molecular cancer theranostic agent. However, delivering a sufficient dosage of Cu(II) to the tumor site and integrating multiple imaging modalities to achieve precise and effective cancer theranostics remains a critical challenge. Herein, an emerging Cu(II)-based nanocomposite has been synthesized for targeted tumor computed tomography (CT)/magnetic resonance (MR) dual-mode imaging and chemodynamic therapy (CDT). Briefly, 2-picolinic acid (PA-COOH), polyethylene glycol (PEG)-linked folic acid (FA), and fluorescein isothiocyanate (FI) were sequentially conjugated with polyethylenimine (PEI.NH2) and then in situ fabrication of gold nanoparticles (Au NPs) occurred within the PEI.NH2 internal cavity. After acetylation of PEI.NH2 terminal amines and Cu(II) complexation, the Cu(II)-based nanocomposites FA-Au/Cu(II) PENPs with a mean diameter of 2.87 nm were generated. The synthesized FA-Au/Cu(II) PENPs showed favorable stability of colloidal dispersion, sustainable Cu(II) release properties in a pH-dependent manner, and Fenton-like catalytic activity specifically. With the FA-mediated targeting pathway, FA-Au/Cu(II) PENPs can specifically accumulate in cancer cells with high expression of FA receptors. Meanwhile, the complementary CT/MR dual-mode imaging in vitro and in vivo can be afforded by FA-Au/Cu(II) PENPs based on the excellent X-ray attenuation properties of Au NPs and the applicable r1 relaxivity (0.7378 mM-1s-1) of Cu(II). Notably, the Cu(II)-mediated CDT mechanism enables FA-Au/Cu(II) PENPs to elicit the generation of toxic hydroxyl radicals (·OH), depletion of glutathione (GSH), promotion of lipid peroxidation (LPO), and induction of cancer cell apoptosis in vitro, and further demonstrates remarkable anti-tumor efficacy in a xenograft tumor model. With the illustrated targeted theranostic capacity of FA-Au/Cu(II) PENPs towards tumors, this Cu(II)-based nanocomposite paradigm inspires the construction of advanced theranostic nanoplatforms incorporating alternative transition metal ions.

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铜(II)络合聚乙烯亚胺包埋金纳米颗粒实现肿瘤的靶向CT/MR成像和化学动力学治疗。
过渡金属离子铜(II) (Cu(II))作为一种小分子癌症治疗剂越来越受到人们的关注。然而,将足够剂量的Cu(II)输送到肿瘤部位并整合多种成像方式以实现精确有效的癌症治疗仍然是一个关键的挑战。本文合成了一种新型的Cu(II)基纳米复合材料,用于靶向肿瘤计算机断层扫描(CT)/磁共振(MR)双模成像和化学动力治疗(CDT)。简单地说,2-吡啶酸(PA-COOH)、聚乙二醇(PEG)连接的叶酸(FA)和异硫氰酸荧光素(FI)依次与聚乙烯亚胺(PEI. nh2)偶联,然后在PEI内原位制备金纳米颗粒(Au NPs)。NH2内腔。在PEI乙酰化后。通过NH2末端胺和Cu(II)络合,制备了平均直径为2.87 nm的Cu(II)基FA-Au/Cu(II) PENPs纳米复合材料。所合成的FA-Au/Cu(II) PENPs具有良好的胶体分散稳定性、持续的ph依赖性Cu(II)释放性能和类fenton催化活性。通过FA介导的靶向途径,FA- au /Cu(II) PENPs可以在FA受体高表达的癌细胞中特异性积累。同时,FA-Au/Cu(II) PENPs基于Au NPs优异的x射线衰减特性和Cu(II)适用的r1弛豫率(0.7378 mM-1s-1),可提供体外和体内互补的CT/MR双模成像。值得注意的是,Cu(II)介导的CDT机制使FA-Au/Cu(II) PENPs在体外诱导毒性羟基自由基(·OH)的产生、谷胱甘肽(GSH)的消耗、脂质过氧化(LPO)的促进和诱导癌细胞凋亡,并进一步在异种移植肿瘤模型中显示出显著的抗肿瘤功效。由于FA-Au/Cu(II) PENPs对肿瘤具有靶向治疗能力,这种基于Cu(II)的纳米复合材料范式激发了构建包含替代过渡金属离子的先进治疗纳米平台的灵感。
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来源期刊
Polymers
Polymers POLYMER SCIENCE-
CiteScore
8.00
自引率
16.00%
发文量
4697
审稿时长
1.3 months
期刊介绍: Polymers (ISSN 2073-4360) is an international, open access journal of polymer science. It publishes research papers, short communications and review papers. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. Therefore, there is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. Polymers provides an interdisciplinary forum for publishing papers which advance the fields of (i) polymerization methods, (ii) theory, simulation, and modeling, (iii) understanding of new physical phenomena, (iv) advances in characterization techniques, and (v) harnessing of self-assembly and biological strategies for producing complex multifunctional structures.
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