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首页> 外文期刊>Molecular pharmaceutics >Indocyanine green-containing nanostructure as near infrared dual-functional targeting probes for optical imaging and photothermal therapy.
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Indocyanine green-containing nanostructure as near infrared dual-functional targeting probes for optical imaging and photothermal therapy.

机译:含吲哚菁绿的纳米结构作为近红外双功能靶向探针,用于光学成像和光热疗法。

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Indocyanine green (ICG) is a near-infrared (NIR) imaging agent and is also an ideal light absorber for laser-mediated photothermal therapy. This NIR dye could serve as a basis of a dual-functional probe with integrated optical imaging and photothermal therapy capabilities. However, applications of ICG remain limited by its concentration-dependent aggregation, poor aqueous stability, nonspecific binding to proteins and lack of target specificity. To overcome these limitations, a novel ICG-containing nanostructure is designed utilizing the noncovalent self-assembly chemistry between phospholipid-polyethylene glycol (PL-PEG) and ICG. The interactions between both amphiphilic ICG and PL-PEG were studied using absorption and fluorescence spectroscopy. The properties of ICG-PL-PEG nanoprobe, such as absorption and fluorescence spectra, stability, morphology and size distribution, were also investigated. Two representative targeting molecules, namely, a small molecule, folic acid (FA), and a large protein, integrin alpha(v)beta monoclonal antibody (mAb), were conjugated to the surface of ICG-PL-PEG nanoprobe, displaying the diversity of ligand conjugation. The target specificity was confirmed using three cell lines with different levels of available folate receptors (FRs) or integrin alpha(v)beta expression via laser scanning confocal microscope and flow cytometry. This targeting ICG-PL-PEG nanoprobe could be internalized into targeted cells via ligand-receptor mediated endocytosis pathway. Our in vitro experiments showed that internalized ICG-PL-PEG could be used for cell imaging and selective photothermal cell destruction. These results represent the first demonstration of the dual functionality of ICG-containing nanostructure for targeted optical imaging and photothermal therapy of cancerous cells. This novel ICG-PL-PEG nanostructure, when conjugated with other therapeutic and imaging agents, could become a multifunctional probe for cancer diagnosis and treatment.
机译:吲哚菁绿(ICG)是近红外(NIR)成像剂,也是激光介导的光热疗法的理想吸光剂。这种NIR染料可以用作具有集成光学成像和光热疗法功能的双功能探针的基础。但是,ICG的应用仍然受到其浓度依赖性聚集,不良的水稳定性,与蛋白质的非特异性结合以及缺乏靶标特异性的限制。为了克服这些限制,利用磷脂-聚乙二醇(PL-PEG)和ICG之间的非共价自组装化学方法,设计了一种新型的含ICG的纳米结构。使用吸收和荧光光谱研究了两亲性ICG和PL-PEG之间的相互作用。还研究了ICG-PL-PEG纳米探针的特性,例如吸收和荧光光谱,稳定性,形态和尺寸分布。两个代表性的靶向分子,即小分子叶酸(FA)和大蛋白整合素α(v)β单克隆抗体(mAb),与ICG-PL-PEG纳米探针的表面偶联,表现出多样性配体结合。通过激光扫描共聚焦显微镜和流式细胞术,使用具有不同水平的可用叶酸受体(FRs)或整联蛋白alpha(v)beta表达的三种细胞系来确认靶标特异性。这种靶向ICG-PL-PEG纳米探针可以通过配体-受体介导的内吞途径内化到靶向细胞中。我们的体外实验表明,内在的ICG-PL-PEG可用于细胞成像和选择性光热细胞破坏。这些结果代表了含ICG的纳米结构对癌细胞的靶向光学成像和光热疗法双重功能的首次展示。这种新颖的ICG-PL-PEG纳米结构与其他治疗剂和成像剂结合后,可成为癌症诊断和治疗的多功能探针。

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