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用于靶向磁共振成像和癌症治疗的多功能超支化聚合物包覆磁铁矿纳米粒子的设计与构建

Design and construction of multifunctional hyperbranched polymers coated magnetite nanoparticles for both targeting magnetic resonance imaging and cancer therapy.

作者信息

Mashhadi Malekzadeh Asemeh, Ramazani Ali, Tabatabaei Rezaei Seyed Jamal, Niknejad Hassan

机构信息

Department of Chemistry, Faculty of Science, University of Zanjan, P.O. Box 45195-313, Zanjan, Iran.

Department of Chemistry, Faculty of Science, University of Zanjan, P.O. Box 45195-313, Zanjan, Iran.

出版信息

J Colloid Interface Sci. 2017 Mar 15;490:64-73. doi: 10.1016/j.jcis.2016.11.014. Epub 2016 Nov 10.

Abstract

Magnetic drug targeting is a drug delivery strategy that can be used to improve the therapeutic efficiency on tumor cells and reduce the side effects on normal cells and tissues. The aim in this study is designing a novel multifunctional drug delivery system based on superparamagnetic nanoparticles for cancer therapy. Magnetic nanoparticles were synthesized by coprecipitation of iron oxide followed by coating with poly citric acid (PCA) dendritic macromolecules via bulk polymerization strategy. It was further surface-functionalized with poly(ethylene glycol) (PEG) and then to achieve tumor cell targeting property, folic acid was further incorporated to the surface of prepared carriers via a facile coupling reaction between the hydroxyl end group of the PEG and the carboxyl group of folic acid. The so prepared nanocarriers (FeO@PCA-PEG-FA) were characterized by X-ray diffraction, TEM, TGA, FT-IR, DLS and VSM techniques. The room temperature VSM measurements showed that magnetic particles were superparamagnetic. Transmission electron microscopy and dynamic light scattering were also performed which revealed that size of nanocarriers was lying in the range of 10-49nm. Quercetin loading and release profiles of prepared nanocarriers showed that up to 83% of loaded drug was released in 250h. Fluorescent microscopy showed that the cellular uptake by folate receptor-overexpressing HeLa cells of the quercetin-loaded FeO@PCA-PEG-FA nanoparticles was higher than that of non-folate conjugated nanoparticles. Thus, folate conjugation significantly increased nanoparticle cytotoxicity. Also, T-weighted MRI images of FeO@PCA-PEG-FA nanoparticles showed that the magnetic resonance signal is enhanced significantly with increasing nanoparticle concentration in water and they also served as MRI contrast agents with relaxivities of 3.4mMs (r) and 99.8mMs (r). The results indicate that this multifunctional nanocarrier is a significant breakthrough in developing a drug delivery vehicle that combines drug targeting as well as sensing and therapy at the same time.

摘要

磁性药物靶向是一种药物递送策略,可用于提高对肿瘤细胞的治疗效率,并减少对正常细胞和组织的副作用。本研究的目的是设计一种基于超顺磁性纳米颗粒的新型多功能药物递送系统用于癌症治疗。通过氧化铁共沉淀法合成磁性纳米颗粒,然后通过本体聚合法用聚柠檬酸(PCA)树枝状大分子进行包覆。进一步用聚乙二醇(PEG)对其进行表面功能化,然后为实现肿瘤细胞靶向特性,通过PEG的羟基端基与叶酸的羧基之间的简便偶联反应,将叶酸进一步掺入所制备载体的表面。通过X射线衍射、透射电子显微镜、热重分析、傅里叶变换红外光谱、动态光散射和振动样品磁强计技术对如此制备的纳米载体(FeO@PCA-PEG-FA)进行了表征。室温振动样品磁强计测量表明磁性颗粒具有超顺磁性。还进行了透射电子显微镜和动态光散射分析,结果显示纳米载体的尺寸在10 - 49nm范围内。所制备纳米载体的槲皮素负载和释放曲线表明,在250小时内高达83%的负载药物被释放。荧光显微镜显示,槲皮素负载的FeO@PCA-PEG-FA纳米颗粒被叶酸受体过表达的HeLa细胞摄取的量高于未与叶酸偶联的纳米颗粒。因此,叶酸偶联显著增加了纳米颗粒的细胞毒性。此外,FeO@PCA-PEG-FA纳米颗粒的T加权磁共振成像显示,随着水中纳米颗粒浓度的增加,磁共振信号显著增强,并且它们还作为磁共振造影剂,弛豫率分别为3.4mMs(r1)和99.8mMs(r2)。结果表明,这种多功能纳米载体在开发同时结合药物靶向以及传感和治疗的药物递送载体方面是一个重大突破。

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