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Transferring Biomarker into Molecular Probe: Melanin Nanoparticle as a Naturally Active Platform for Multimodality Imaging

机译:将生物标志物转移到分子探针中:黑色素纳米颗粒作为多模态成像的天然活性平台。

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摘要

Developing multifunctional and easily prepared nanoplatforms with integrated different modalities is highly challenging for molecular imaging. Here, we report the successful transfer of an important molecular target, melanin, into a novel multimodality imaging nanoplatform. Melanin is abundantly expressed in melanotic melanomas and thus has been actively studied as a target for melanoma imaging. In our work, the multifunctional biopolymer nanoplatform based on ultrasmall (<10 nm) water-soluble melanin nanoparticle (MNP) was developed and showed unique photoacoustic property and natural binding ability with metal ions (for example, ~(64)Cu~(2+), Fe~(3+)). Therefore, MNP can serve not only as a photoacoustic contrast agent, but also as a nanoplatform for positron emission tomography (PET) and magnetic resonance imaging (MRI). Traditional passive nanoplatforms require complicated and time-consuming processes for prebuilding reporting moieties or chemical modifications using active groups to integrate different contrast properties into one entity. In comparison, utilizing functional biomarker melanin can greatly simplify the building process. We further conjugated α_vβ_3 integrins, cyclic c(RGDfC) peptide, to MNPs to allow for U87MG tumor accumulation due to its targeting property combined with the enhanced permeability and retention (EPR) effect. The multimodal properties of MNPs demonstrate the high potential of endogenous materials with multifunctions as nanoplatforms for molecular theranostics and clinical translation.
机译:对于分子成像而言,开发具有集成不同模式的多功能且易于制备的纳米平台是极具挑战性的。在这里,我们报告成功地将重要的分子靶标黑色素成功转移到新型多模态成像纳米平台中。黑色素在黑色素性黑色素瘤中大量表达,因此已经被积极研究作为黑色素瘤成像的靶标。在我们的工作中,开发了基于超小(<10 nm)水溶性黑色素纳米颗粒(MNP)的多功能生物聚合物纳米平台,该平台具有独特的光声性质和与金属离子的自然结合能力(例如〜(64)Cu〜(2 +),Fe〜(3+))。因此,MNP不仅可以用作光声造影剂,还可以用作正电子发射断层扫描(PET)和磁共振成像(MRI)的纳米平台。传统的被动纳米平台需要复杂且耗时的过程,以使用活性基团将不同的对比度特性整合到一个实体中来预先构建报告部分或化学修饰。相比之下,利用功能性生物标志物黑色素可以大大简化构建过程。我们进一步将α_vβ_3整合素,环状c(RGDfC)肽缀合到MNP,以允许U87MG肿瘤积累,这是由于其靶向特性以及增强的通透性和保留(EPR)效应。 MNPs的多峰性质表明具有作为纳米平台的多功能的内源性材料具有很高的潜力,可用于分子治疗学和临床翻译。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2014年第43期|15185-15194|共10页
  • 作者单位

    Molecular Imaging Program at Stanford (MIPS), Canary Center at Stanford for Cancer Early Detection, Department of Radiology and Bio-X Program, School of Medicine, Stanford University, Stanford, California 94305-5484, United States,Key Laboratory for Organic Electronics & Information Displays and Institute of Advanced Materials, Nanjing University of Posts & Telecommunications, Nanjing 210046, China;

    Molecular Imaging Program at Stanford (MIPS), Canary Center at Stanford for Cancer Early Detection, Department of Radiology and Bio-X Program, School of Medicine, Stanford University, Stanford, California 94305-5484, United States;

    Molecular Imaging Program at Stanford (MIPS), Canary Center at Stanford for Cancer Early Detection, Department of Radiology and Bio-X Program, School of Medicine, Stanford University, Stanford, California 94305-5484, United States;

    Molecular Imaging Program at Stanford (MIPS), Canary Center at Stanford for Cancer Early Detection, Department of Radiology and Bio-X Program, School of Medicine, Stanford University, Stanford, California 94305-5484, United States;

    Molecular Imaging Program at Stanford (MIPS), Canary Center at Stanford for Cancer Early Detection, Department of Radiology and Bio-X Program, School of Medicine, Stanford University, Stanford, California 94305-5484, United States;

    Molecular Imaging Program at Stanford (MIPS), Canary Center at Stanford for Cancer Early Detection, Department of Radiology and Bio-X Program, School of Medicine, Stanford University, Stanford, California 94305-5484, United States;

    Key Laboratory for Organic Electronics & Information Displays and Institute of Advanced Materials, Nanjing University of Posts & Telecommunications, Nanjing 210046, China;

    Department of Radiation Oncology, School of Medicine, Stanford University, Stanford, California 94305, United States;

    Key Laboratory for Organic Electronics & Information Displays and Institute of Advanced Materials, Nanjing University of Posts & Telecommunications, Nanjing 210046, China;

    Molecular Imaging Program at Stanford (MIPS), Canary Center at Stanford for Cancer Early Detection, Department of Radiology and Bio-X Program, School of Medicine, Stanford University, Stanford, California 94305-5484, United States;

    Molecular Imaging Program at Stanford (MIPS), Canary Center at Stanford for Cancer Early Detection, Department of Radiology and Bio-X Program, School of Medicine, Stanford University, Stanford, California 94305-5484, United States;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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  • 入库时间 2022-08-18 03:11:15

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