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Synthesis, optical and morphological characterization of CdSe/ZnSe quantum dots for cytotoxicity studies

机译:用于细胞毒性研究的Cdse / Znse量子点的合成,光学和形态表征

摘要

Colon cancer (CC) ranks high in morbidity and mortality amongst the most frequent occurring cancers worldwide. Mortality rates are mostly caused by mis-diagnosis and the poor efficacy of treatment. The aim of this study was to enhance our insights of quantum dots, for early detection and targeted drug delivery, thereby reducing toxicity to normal cells and reducing side effects that are caused by previous colon cancer medicine. The synthesis, characterization and cytotoxicity studies of CdSe/ZnSe quantum dots (QDs), nanocrystals are reported. Toxicological properties of the Cd2+ core are reduced by capping quantum dots with ZnSe, varying chain length and functional group ligands. Fluorescence wavelength and their size is improved by varying Cd2+ source and varying nanocrystal synthesis growth temperature. CdSe/ZnSe quantum dots are characterized with FT-IR to elucidate their structure. High-resolution transmission electron microscopy (HRTEM), X-Ray Diffraction (EDX), Photoluminescence spectroscopy (PL) and Ultraviolet-visible spectroscopy (UV-Vis) are used to measure their size and composition. Ligand exchange reactions are conducted with the use of 3-Mercaptopropanoic acid (3-MPA) to facilitate bio-compatibility and stability of CdSe/ZnSe QDs. Temperature stability of various ligand capped and stabilized CdSe/ZnSe QDs are measured by using thermogravimetric analysis (TGA). Caco-2 cell line is cultured from colon cancer, and cytotoxic studies are conducted to test for cell viability of various capped 3-Mercaptopropanoic acid (3-MPA) CdSe/ZnSe quantum dots at various concentrations. Myristic acid capped CdSe/ZnSe quantum dots produce high fluorescing mono-disperse quantum dots. The capping material, synthesis temperature and Cd2+ source of CdSe/ZnSe QDs affect fluorescence wavelength and thermal stability of quantum dots. Fluorescence wavelength is improved by using CdCl2.7H2O source of Cd2+. Cytotoxicity was found to be dependent on the concentration and the capping material of quantum dots. CdSe/ZnSe quantum dots toxicity is adjusted and reduced by varying the length, size and type of the capping ligand on the surface of quantum dots.
机译:在全球最常见的癌症中,结肠癌(CC)的发病率和死亡率高。死亡率主要是由于误诊和治疗效果差所致。这项研究的目的是增强我们对量子点的认识,以便及早发现和靶向药物递送,从而减少对正常细胞的毒性并减少以前的结肠癌药物引起的副作用。报道了CdSe / ZnSe量子点(QDs),纳米晶体的合成,表征和细胞毒性研究。通过用ZnSe覆盖量子点,改变链长和官能团配体,可以降低Cd2 +核的毒理学性质。改变Cd2 +的来源和改变纳米晶体的合成生长温度可以改善荧光波长及其尺寸。利用FT-IR对CdSe / ZnSe量子点进行了表征,以阐明其结构。高分辨率透射电子显微镜(HRTEM),X射线衍射(EDX),光致发光光谱(PL)和紫外可见光谱(UV-Vis)用于测量其尺寸和组成。使用3-巯基丙酸(3-MPA)进行配体交换反应,以促进CdSe / ZnSe QD的生物相容性和稳定性。使用热重分析(TGA)测量各种配体封端和稳定的CdSe / ZnSe QD的温度稳定性。从结肠癌培养Caco-2细胞系,并进行细胞毒性研究,以测试各种浓度的各种加帽的3-巯基丙酸(3-MPA)CdSe / ZnSe量子点的细胞活力。肉豆蔻酸封端的CdSe / ZnSe量子点产生高荧光的单分散量子点。 CdSe / ZnSe QD的覆盖材料,合成温度和Cd2 +来源会影响荧光波长和量子点的热稳定性。通过使用Cd2 +的CdCl2.7H2O光源可以改善荧光波长。发现细胞毒性取决于量子点的浓度和封端材料。通过改变量子点表面上封端配体的长度,大小和类型,可以调节和降低CdSe / ZnSe量子点的毒性。

著录项

  • 作者

    Nkaule Anati Nomxolisi;

  • 作者单位
  • 年度 2013
  • 总页数
  • 原文格式 PDF
  • 正文语种 English
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