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合成可调谐多功能 Ni 掺杂近红外 QDs 用于癌细胞靶向和细胞分选。

Synthesis of tunable and multifunctional Ni-doped near-infrared QDs for cancer cell targeting and cellular sorting.

机构信息

Research Center for Applied Sciences, Academia Sinica, Taipei 115, Taiwan.

出版信息

Bioconjug Chem. 2012 Mar 21;23(3):421-30. doi: 10.1021/bc200435e. Epub 2012 Feb 17.

DOI:10.1021/bc200435e
PMID:22304752
Abstract

Here, we report the facile preparation of tunable magnetic Ni-doped near-infrared (NIR) quantum dots (MNIR-QDs) as an efficient probe for targeting, imaging, and cellular sorting applications. We synthesized the MNIR-QDs via a hot colloidal synthesis approach to yield monodisperse and tunable QDs. These hydrophobic QDs were structurally and compositionally characterized and further functionalized with amino-PEG and carboxyl-PEG to improve their biocompatibility. Since QDs are known to be toxic due to the presence of cadmium, we have evaluated the in vitro and in vivo toxicity of our surface-functionalized MNIR-QDs. Our results revealed that surface-functionalized MNIR-QDs did not exhibit significant toxicity at the concentrations used in the experiments and are therefore suitable for biological applications. For further in vitro applications, we covalently linked folic acid to the surface of amino-PEG-coated MNIR-QDs through NHS chemistry to target the folate receptors largely present in the HeLa cells to demonstrate the specific targeting and magnetic behavior of these MNIR-QDs. Improved specificity has been observed with treatment of HeLa cells with the folic acid-linked amino PEG-coated MNIR QDs (FA-PEG-MNIR-QDs) compared to the one without folic acid. Since the synthesized probe has magnetic property, we have also successfully demonstrated sorting between the cells which have taken up the probe with the use of a magnet. Our findings strongly suggest that these functionalized MNIR-QDs can be a potential probe for targeting, cellular sorting, and bioimaging applications.

摘要

在这里,我们报告了一种简便的方法来制备可调谐磁性 Ni 掺杂近红外(NIR)量子点(MNIR-QDs),作为用于靶向、成像和细胞分选应用的有效探针。我们通过热胶体合成方法合成了 MNIR-QDs,得到了单分散且可调谐的 QDs。对这些疏水性 QDs 进行了结构和组成表征,并进一步用氨基-PEG 和羧基-PEG 功能化,以提高其生物相容性。由于 QDs 由于存在镉而具有毒性,因此我们评估了我们表面功能化的 MNIR-QDs 的体外和体内毒性。我们的结果表明,在实验中使用的浓度下,表面功能化的 MNIR-QDs 没有表现出明显的毒性,因此适合生物应用。为了进一步进行体外应用,我们通过 NHS 化学将叶酸通过 NHS 化学共价连接到氨基-PEG 包覆的 MNIR-QDs 表面,以针对大量存在于 HeLa 细胞中的叶酸受体,证明这些 MNIR-QDs 的特异性靶向和磁性行为。与没有叶酸的 MNIR-QDs 相比,用叶酸连接的氨基-PEG 包覆的 MNIR-QDs(FA-PEG-MNIR-QDs)处理 HeLa 细胞时,观察到了更好的特异性。由于合成的探针具有磁性,我们还成功地使用磁铁在摄取了探针的细胞之间进行了分选。我们的研究结果强烈表明,这些功能化的 MNIR-QDs 可以成为靶向、细胞分选和生物成像应用的潜在探针。

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