首页> 外文会议>Proceedings of the ASME international mechanical engineering congress and exposition 2009 >NANOPARTICLE-APTAMER: AN EFFECTIVE GROWTH INHIBITOR FOR HUMAN CANCER CELLS
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NANOPARTICLE-APTAMER: AN EFFECTIVE GROWTH INHIBITOR FOR HUMAN CANCER CELLS

机译:纳米粒子-适体:一种有效的人类癌细胞生长抑制剂

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Semiconductor nanocrystals have unique optical properties due to quantum confinement effects, and a variety of promising approaches have been devised to interface the nanomaterials with biomolecules for bioimaging and therapeutic applications. Such bio-interface can be facilitated via a DNA template for nanoparticles as oligonucleotides can mediate the aqueous-phase nucleation and capping of semiconductor nanocrystals.rnHere, we report a novel scheme of synthesizing fluorescent nanocrystal quantum dots (NQDs) using DNA aptamers and the use of this biotic/abiotic nanoparticle system for growth inhibition of MCF-7 human breast cancer cells for the first time. Particularly, we used two DNA sequences for this purpose, which have been developed as anti-cancer agents: ~5-GGT GGT GGT GGT TGT GGT GGT GGT GG-~3 (also called, AGRO) and ~5-(GT)_(15)-~3.~([3-5]) This study may ultimately form the basis of unique nanoparticle-based therapeutics with the additional ability to optically report molecular recognition.rnFigure la shows the photoluminescence (PL) spectra of GT- and AGRO-passivated PbS QD that fluoresce in the near IR, centered at approximately 980 run. A typical synthesis procedure involves rapid addition of sodium sulfide in the mixture solution of DNA and Pb acetate at a molar ratio of 2:4:1. The resulting nanocrystals are washed to remove unreacted DNA and ions by adding mixture solution of NaCl and isopropanol, followed by centrifugation. The precipitated nanocrystals are collected and re-suspended in aqueous solution by mild sonication. Optical absorption measurements reveal that approximately 90 and 77% of GT and AGRO DNA is removed after the washing process. The particle size distribution in Figure 1b suggests that the GT sequence-capped PbS particles are primarily in 3-5 nm diameter range. These nanocrystals can be easily incorporated with mammalian cellsrnand remain highly fluorescent in sub-cellular environments. Figure 1c serially presents an optical image of a MCF-7 cell and a PL image of the AGRO-capped QD incorporated with the cell.
机译:半导体纳米晶体由于量子限制效应而具有独特的光学性质,并且已经设计出各种有前途的方法来使纳米材料与生物分子对接,以用于生物成像和治疗应用。通过寡核苷酸可以介导水相成核和封盖半导体纳米晶体的纳米粒子的DNA模板,可以促进这种生物界面。在这里,我们报道了一种使用DNA适体合成荧光纳米晶体量子点(NQD)的新方案,这种生物/非生物纳米颗粒系统首次用于抑制MCF-7人乳腺癌细胞的生长。特别地,我们为此目的使用了两个DNA序列,它们已被开发为抗癌剂:〜5-GGT GGT GGT GGT TGT GGT GGT GGT GG-〜3(也称为AGRO)和〜5-(GT)_ (15)-〜3.〜([3-5])该研究最终可能形成独特的基于纳米颗粒的疗法,并具有光学报告​​分子识别的附加功能。图1a显示了GT-的光致发光(PL)光谱AGRO钝化的PbS QD在近红外处发出荧光,中心波长约为980 nm。典型的合成步骤包括以2:4:1的摩尔比在DNA和乙酸铅的混合溶液中快速添加硫化钠。通过添加NaCl和异丙醇的混合溶液,洗涤得到的纳米晶体以除去未反应的DNA和离子,然后离心。收集沉淀的纳米晶体,并通过轻度超声将其重新悬浮在水溶液中。吸光度测量表明,洗涤过程后大约90%和77%的GT和AGRO DNA被去除。图1b中的粒度分布表明,GT序列封端的PbS颗粒主要在3-5 nm的直径范围内。这些纳米晶体可以很容易地与哺乳动物细胞结合,并在亚细胞环境中保持高度荧光。图1c连续显示了MCF-7电池的光学图像和与该电池结合的AGRO封顶的QD的PL图像。

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