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In vivo MRI detection of gliomas by chlorotoxin-conjugated superparamagnetic nanoprobes

机译:氯毒素缀合的超顺磁性纳米探针的体内MRI检测胶质瘤

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Converging advances in the development of nanoparticle-based imaging probes and improved understanding of the molecular biology of brain tumors offer the potential to provide physicians with new tools for the diagnosis and treatment of these deadly diseases. However, the effectiveness of promising nanoparticle technologies is currently limited by insufficient accumulation of these contrast agents within tumors. Here a biocompatible nanoprobe composed of a poly(ethylene glycol) (PEG) coated iron oxide nanoparticle that is capable of specifically targeting glioma tumors via the surface-bound targeting peptide, chlorotoxin (CTX), is presented. The preferential accumulation of the nanoprobe within gliomas and subsequent magnetic resonance imaging (MRI) contrast enhancement are demonstrated in vitro in 9L cells and in vivo in tumors of a xenograft mouse model. TEM imaging reveals that the nanoprobes are internalized into the cytoplasm of 9L cells and histological analysis of selected tissues indicates that there are no acute toxic effects of these nanoprobes. High targeting specificity and benign biological response establish this nanoprobe as a potential platform to aid in the diagnosis and treatment of gliomas and other tumors of neuroectodermal origin.
机译:基于纳米粒子的成像探针开发的不断进步和对脑肿瘤分子生物学的更好理解为医生提供了诊断和治疗这些致命疾病的新工具。然而,当前有前景的纳米颗粒技术的有效性受到这些造影剂在肿瘤中的不足累积的限制。在这里,提出了一种生物相容性纳米探针,该探针由聚(乙二醇)(PEG)包覆的氧化铁纳米颗粒组成,能够通过表面结合的靶向肽氯毒素(CTX)特异性靶向神经胶质瘤。胶质瘤中纳米探针的优先积累和随后的磁共振成像(MRI)对比增强已在体外9L细胞中和体内异种移植小鼠模型的肿瘤中得到证实。 TEM成像显示纳米探针被内化到9L细胞的细胞质中,对选定组织的组织学分析表明这些纳米探针没有急性毒性作用。高靶向特异性和良性生物学反应使这种纳米探针成为潜在的平台,可帮助诊断和治疗神经胶质瘤和其他神经外胚层起源的肿瘤。

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