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Surface design and preparation of multi-functional magnetic nanoparticles for cancer cell targeting, therapy, and imaging

机译:用于癌细胞靶向,治疗和成像的多功能磁性纳米粒子的表面设计和制备

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Recently, theranostic candidates based on superparamagnetic iron oxide nanoparticles (SPIONs) providing the combination of therapy and diagnosis have become one of the most promising system in cancer research. However, poor stability, premature drug release, lack of specific tumor cell targeting, and complicated multi-step synthesis processes still hinder them for potential clinical applications. In this research, the multi-functional magnetic nanoparticles (MNPs-DOX) were prepared via a simple assembly process for targeted delivery of doxorubicin (DOX) and enhanced magnetic resonance (MR) imaging detection. Firstly, the multi-functional copolymer coating, polyamidoamine (PAMAM), was designed and synthesized by Michael addition reaction, where N , N -bis(acryloyl)cystamine served as backbone linker, and DOX, dopamine (DA), and polyethylene glycol (PEG) acted as comonomers. The PAMAM was then directly assembled to the surface of SPIONs by the ligand exchange reaction with SPIONs forming the MNPs-DOX. The hydrophilic PEG moieties provide the nanoparticles with colloidal stability and good-dispersity in aqueous solution. Comparing with the quick release of free DOX, the drug release behavior of MNPs-DOX exhibited a sustained drug release. Because the chemical cleavage of disulfide in the polymer backbone, a high cumulative drug release up to 60% in GSH within 48 h was observed, rather than only 26% in PBS (pH 7.4) without GSH. The MR imaging detection experiment showed that the MNPs-DOX had an enhanced T _(2) relaxivity of 126 mM ~(?1) S ~(?1) for MR imaging. The results of the cytotoxicity assays showed a remarkable killing effect of cancer cells by MNPs-DOX due to the FA tumor-targeting ligand, comparing with non-targeted drug molecules. All the results showed that the as prepared multi-functional magnetic nanoparticles may serve as a promising theranostic candidate for targeted anticancer drug delivery and efficient detection through MR imaging in medical application.
机译:最近,基于超顺磁性氧化铁纳米粒子(SPIONs)的治疗学候选物提供了治疗和诊断的结合,已成为癌症研究中最有前途的系统之一。然而,差的稳定性,过早的药物释放,缺乏特异性的肿瘤细胞靶向以及复杂的多步合成过程仍然阻碍它们用于潜在的临床应用。在这项研究中,多功能磁性纳米颗粒(MNPs-DOX)是通过简单的组装过程制备的,用于靶向递送阿霉素(DOX)和增强磁共振(MR)成像检测。首先,通过迈克尔加成反应设计合成了多功能共聚物涂料聚酰胺酰胺(PAMAM),其中N,N-双(丙烯酰基)胱胺为骨架连接物,DOX,多巴胺(DA)和聚乙二醇PEG)充当共聚单体。然后通过与形成MNPs-DOX的SPION的配体交换反应将PAMAM直接组装到SPION的表面。亲水性PEG部分为纳米颗粒提供了胶体稳定性和在水溶液中的良好分散性。与游离DOX的快速释放相比,MNPs-DOX的药物释放行为表现出持续的药物释放。由于二硫键在聚合物主链中发生了化学裂解,因此在48小时内在GSH中观察到了高达60%的高累积药物释放,而在没有GSH的PBS(pH 7.4)中仅观察到26%的药物释放。 MR成像检测实验表明,MNPs-DOX的MR成像具有126 mM〜(?1)S〜(?1)的增强的T_(2)弛豫度。细胞毒性试验的结果显示,与非靶向药物分子相比,由于FA肿瘤靶向配体,MNPs-DOX可以显着杀死癌细胞。所有结果表明,所制备的多功能磁性纳米粒子可作为有前景的治疗学候选物,用于靶向抗癌药物的递送以及在医学应用中通过MR成像进行有效检测。

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