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Immunolabeling and NIR-excited fluorescent imaging of HeLa cells by using NaYF_4:Yb,Er upconversion nanoparticles

机译:NaYF_4:Yb,Er上转换纳米粒子对HeLa细胞的免疫标记和NIR激发荧光成像

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Upconversion fluorescent nanoparticles can convert a longer wavelength radiation (e.g., nearinfrared light) into a shorter wavelength fluorescence (e.g., visible light) and thus have emerged as a new class of fluorescent probes for biomedical imaging. Rare-earth doped β-NaYF_4:Yb,Er upconversion nanoparticles (UCNPs) with strong UC fluorescence were synthesized in this work by using a solvothermal approach. The UCNPs were coated with a thin layer of SiO_2 to form core-shell nanoparticles via a typical St?ber method, which were further modified with amino groups. After surface functionalization, the rabbit anti-CEA8 antibodies were covalently linked to the UCNPs to form the antibody-UCNP conjugates. The antibody-UCNP conjugates were used as fluorescent biolabels for the detection of carcinoembryonic antigen (CEA), a cancer biomarker expressed on the surface of HeLa cells. The successful conjugation of antibody to the UCNPs was found to lead to the specific attachment of the UCNPs onto the surface of the HeLa cells, which further resulted in the bright green UC fluorescence from the UCNP-labeled cells under 980 nm near-infrared (NIR) excitation and enabled the fluorescent imaging and detection of the HeLa cells. These results indicate that the amino-functionalized UCNPs can be used as fluorescent probes in cell immunolabeling and imaging. Because the UCNPs can be excited with a NIR light to exhibit strong visible fluorescence and the NIR light is safe to the body and can penetrate tissue as deep as several inches, our work suggests that, with proper cell-targeting or tumor-homing peptides or proteins conjugated, the NaYF_4:Yb,Er UCNPs can find potential applications in the in vivo imaging, detection, and diagnosis of cancers.
机译:上转换荧光纳米颗粒可以将较长波长的辐射(例如,近红外光)转换为较短波长的荧光(例如,可见光),因此已经成为用于生物医学成像的新型荧光探针。通过溶剂热法合成了稀土掺杂的β-NaYF_4:Yb,具有较强的UC荧光的Er上转换纳米粒子(UCNPs)。 UCNPs通过典型的St?ber方法涂有SiO_2薄层以形成核-壳纳米颗粒,并用氨基进一步修饰。在表面功能化之后,将兔抗CEA8抗体共价连接至UCNP,以形成抗体-UCNP缀合物。抗体-UCNP偶联物用作荧光生物标记物,用于检测癌胚抗原(CEA),这是一种在HeLa细胞表面表达的癌症生物标志物。发现抗体与UCNP的成功偶联导致UCNP特异性附着在HeLa细胞表面上,这进一步导致来自UCNP标记的细胞在980 nm近红外(NIR)下发出亮绿色的UC荧光。 )激发并实现了HeLa细胞的荧光成像和检测。这些结果表明,氨基官能化的UCNP可以用作细胞免疫标记和成像中的荧光探针。由于UCNP可以被近红外光激发而显示出强大的可见荧光,并且近红外光对于人体是安全的,并且可以穿透深达几英寸的组织,因此我们的研究表明,使用适当的细胞靶向肽或肿瘤归巢肽或NaYF_4:Yb,Er UCNPs偶联的蛋白质可以在体内成像,检测和诊断癌症中找到潜在的应用。

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