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Aminosilane Functionalization and Cytotoxicity Effects of Upconversion Nanoparticles Y2O3 and Gd2O3 Co-Doped with Yb3+and Er3+

机译:Yb3 +和Er3 +共掺杂的上转换纳米粒子Y2O3和Gd2O3的氨基硅烷官能化和细胞毒性作用

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摘要

In this study, luminescent upconversion nanoparticles (UCNPs) Y2O3 and Gd2O3 co-doped with Yb3+ and Er3+ were prepared by the sol-gel method (SG). These NPs are able to absorb near infrared photons and upconvert them into visible radiation with a direct application in bioimaging, as an important tool to diagnose and visualize cancer cells. The UCNPs were coated with a thin silica shell and functionalized with amino groups for further folic acid conjugation to allow their interaction with folate ligands on the cell surface. Their physical properties were analysed by Transmission Electron Microscopy (TEM), Fourier transform infrared spectroscopy (FTIR) and photoluminescence (PL) measurements. The PL results revealed excellent luminescence properties on all core-shell UCNPs. Cytotoxicity experiments with concentrations of bare and aminosilane coated/functionalized UCNPs between 0.001 μg/mL to 1 μg/mL were tested on two different cell lines from human cervix carcinoma (HeLa) and human colorectal adenocarcinoma (DLD-1) with a colorimetric assay based on the reduction of MTT reagent (methy-134-thiazolyltetrazolium). The assays show that some concentrations of bare UCNPs were cytotoxic for cervical adenocarcinoma cells (HeLa); however, for human colorectal adenocarcinoma all UCNPs are non-cytotoxic. After UCNPs functionalization with silica-aminosilane (APTES/TEOS), all of the nanoparticles tested were found to be non-cytotoxic for both cell lines. The UCNPs functionalized in this work can be further conjugated with specific ligands and used as biolabels for detection of cancer cells.
机译:本研究采用溶胶-凝胶法(SG)制备了Yb 3 + 和Er 3 + 共掺杂的发光上转换纳米粒子(UCNPs)Y2O3和Gd2O3。这些NP能够吸收近红外光子并将其直接转换为可见辐射,并直接应用于生物成像,作为诊断和可视化癌细胞的重要工具。 UCNPs涂有薄的二氧化硅壳,并用氨基官能化以进一步与叶酸结合,以使其与细胞表面的叶酸配体相互作用。通过透射电子显微镜(TEM),傅立叶变换红外光谱(FTIR)和光致发光(PL)测量分析了它们的物理性质。 PL结果显示所有核壳UCNP均具有出色的发光性能。在基于人宫颈癌(HeLa)和人结肠直肠腺癌(DLD-1)的两种不同细胞系上,基于比色测定法对裸露的和氨基硅烷包被的/官能化的UCNPs浓度在0.001μg/ mL至1μg/ mL之间的细胞毒性实验进行了测试还原MTT试剂(甲基-134-噻唑基四唑)。分析表明,某些浓度的裸露UCNP对宫颈腺癌细胞(HeLa)具有细胞毒性。但是,对于人类大肠腺癌,所有的UCNP都是无细胞毒性的。在使用二氧化硅-氨基硅烷(APTES / TEOS)对UCNPs进行功能化后,发现所有测试的纳米颗粒对两种细胞系均无细胞毒性。在这项工作中功能化的UCNP可以进一步与特定的配体缀合,并用作检测癌细胞的生物标记。

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