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首页> 外文期刊>Sensors and Actuators >Aconitic acid derived carbon dots: Conjugated interaction for the detection of folic acid and fluorescence targeted imaging of folate receptor overexpressed cancer cells
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Aconitic acid derived carbon dots: Conjugated interaction for the detection of folic acid and fluorescence targeted imaging of folate receptor overexpressed cancer cells

机译:oni酸衍生的碳点:共轭相互作用,用于检测叶酸和叶酸受体过表达的癌细胞的荧光靶向成像

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摘要

Herein, we utilized aconitic acid (AA) as the precursor for preparing carbon dots (AA-CDs) by a facile hydrothermal reaction, and the resulting AA-CDs exhibited bright blue fluorescence with an absolute quantum yield of 56.5% in aqueous solution. Preliminary experiments showed that the prepared AA-CDs without further surface passivation or modification could selectively interact with folic acid (FA), resulting in significant fluorescence quenching. Based on this, a sensitive method for FA analysis was developed with a detection limit of 40 nM (S/N = 3), which was then successfully applied for the detection of FA in food and pharmaceutical samples with the average recoveries of 95.0–105.3%. Furthermore, a weak fluorescent nanoprobe (FA-AA-CDs) was fabricated based on the conjugated interaction of FA and AA-CDs, and its feasibility was evaluated as a fluorescence turn-on nanoprobe for targeted imaging of cancer cells using Hela, SMMC-7721, and A549 cells as models that expressed different levels of folate receptors (FRs) on the cell surface. The results exhibited that the fluorescence intensity of these cells was in accordance with their FRs expression levels, testifying its potential of FA-AA-CDs for targeted imaging of cancer cells. Subsequently, the internalization mechanism of FA-AA-CDs into cells was elucidated via receptor-mediated endocytosis using control experiments.
机译:在此,我们利用乌头酸(AA)作为前体,通过简便的水热反应制备碳点(AA-CD),所得AA-CD在水溶液中显示出亮蓝色荧光,绝对量子产率为56.5%。初步实验表明,制备的AA-CD无需进一步的表面钝化或修饰即可与叶酸(FA)选择性相互作用,从而导致明显的荧光猝灭。在此基础上,开发了一种灵敏的FA分析方法,其检出限为40 nM(S / N = 3),然后成功地用于食品和药品样品中FA的检测,平均回收率为95.0–105.3 %。此外,基于FA和AA-CD的共轭相互作用,制备了弱荧光纳米探针(FA-AA-CD),并使用Hela,SMMC-S作为荧光靶向纳米探针对癌细胞进行靶向成像,评估了其可行性。 7721和A549细胞作为模型在细胞表面表达不同水平的叶酸受体(FRs)。结果表明,这些细胞的荧光强度与它们的FRs表达水平一致,证明了FA-AA-CDs在癌细胞靶向成像中的潜力。随后,使用对照实验通过受体介导的内吞作用阐明了FA-AA-CDs进入细胞的内在机制。

著录项

  • 来源
    《Sensors and Actuators》 |2018年第6期|444-451|共8页
  • 作者单位

    State Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University;

    State Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University;

    State Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University;

    State Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University;

    School of Pharmacy, Lanzhou University;

    State Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Aconitic acid; Carbon dots; Folic acid; Folate receptor; Cancer cell; Cell imaging;

    机译:乌头酸;碳点;叶酸;叶酸受体;癌细胞;细胞显像;

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