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将 Fe3O4 纳米颗粒开发成一种高效的多模态成像和治疗探针。

Developing Fe3O4 nanoparticles into an efficient multimodality imaging and therapeutic probe.

机构信息

Department of Materials Science and Engineering, College of Engineering, Peking University, Beijing 100871, China.

出版信息

Nanoscale. 2013 Dec 7;5(23):11954-63. doi: 10.1039/c3nr04157c.

Abstract

A rapid ligand-exchange method was developed to transfer high quality hydrophobic magnetite nanocrystals into water-soluble NPs by using protocatechuic acid as a ligand via homogenous reaction. After ligand exchange, the magnetite nanocrystals not only exhibited outstanding stability in water, but also maintained high crystallinity and saturation magnetization. Cell viability experiments demonstrated good biocompatibility of the NPs. For 12 nm magnetite nanoparticles (NPs), the small hydrodynamic size of 14 nm enabled a high T1 relaxivity of 17.8 mM(-1) s(-1) while high saturation magnetization of 77.8 emu g(-1) enabled the NPs to exhibit a high T2 relaxivity of 220 mM(-1) s(-1) in MRI phantom experiments. In vivo MR imaging experiments further confirmed that the NPs were eminent T1 and T2 contrast agents. Moreover, the high quality NPs can be used as excellent magnetic heating agents under an alternating magnetic field. With all those features, including multimodality imaging and magnetic hyperthermia, the NPs can be used as single compound multifunctional agents for various biomedical applications, especially for cancer diagnosis and therapy.

摘要

一种快速配体交换方法被开发出来,通过均相反应,将高质量的疏水性磁铁矿纳米晶体通过原儿茶酸作为配体转化为水溶性 NPs。配体交换后,磁铁矿纳米晶体不仅在水中表现出优异的稳定性,而且保持了高结晶度和饱和磁化强度。细胞活力实验证明了 NPs 的良好生物相容性。对于 12nm 的磁铁矿纳米颗粒(NPs),14nm 的小水动力粒径使得 T1 弛豫率高达 17.8mM(-1)s(-1),而 77.8emu g(-1)的高饱和磁化强度使得 NPs 在 MRI 造影剂实验中表现出 220mM(-1)s(-1)的高 T2 弛豫率。体内磁共振成像实验进一步证实,这些 NPs 是优秀的 T1 和 T2 造影剂。此外,高质量的 NPs 可在交变磁场下用作优异的磁热疗剂。具有多模态成像和磁热疗等特性,这些 NPs 可用作单一化合物多功能试剂,用于各种生物医学应用,特别是癌症的诊断和治疗。

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