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Preparation of size tunable, glutathione-responsive hyaluronic acid-quantum dot nanohybrids using microemulsion method

机译:用微乳液法制备尺寸可调的谷胱甘肽反应性透明质酸-量子点纳米杂化物

摘要

In this paper, a new method for preparing hyaluronic acid-quantum dot (HA-QD) nanohybrids, which are highly monodispersed, colloidally stable, glutathione (GSH)-responsive and size tunable from 80-500 nm, is reported. Due to the fact that HA is a naturally exist polymer and many types of cancer cells are overexpressed with HA receptors on their surfaces, HA has become one of the promising materials to prepare nanocarriers for theranostics applications. Our design is based on the disulfide chemical structure of cystamine dihydrochloride which has been served as the crosslinker. HA-QDs were synthesized in the nano-cavities created by the microemulsion system. The prepared HA-QDs are GSH-responsive. In the presence of GSH, the disulfide bonds can be cleaved and it leads to the degradation of HA-QDs into smaller fragments. Our in vitro studies show that the HA-QDs are highly specific to the pancreatic and cervix cancer cells and no toxicity was detected in the cell proliferation (MTS) assays, revealing the great potentials to use HA-based nanohybrids for cancer imaging and therapy.
机译:本文报道了一种新的制备透明质酸-量子点(HA-QD)纳米杂交体的新方法,该复合体具有高度单分散性,胶体稳定性,谷胱甘肽(GSH)响应性且可在80-500 nm范围内调节大小。由于HA是天然存在的聚合物,并且许多类型的癌细胞在其表面上过度表达HA受体,因此HA已成为制备用于治疗学应用的纳米载体的有前途的材料之一。我们的设计基于胱胺二盐酸盐的二硫键化学结构,该结构已用作交联剂。 HA-QD在由微乳液系统产生的纳米腔中合成。制备的HA-QD对GSH敏感。在谷胱甘肽存在下,二硫键可被切割,并导致HA-QD降解成更小的片段。我们的体外研究表明,HA-QD对胰腺癌细胞和宫颈癌细胞具有高度特异性,并且在细胞增殖(MTS)分析中未检测到毒性,这表明使用基于HA的纳米杂交物进行癌症成像和治疗的巨大潜力。

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