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Preliminary Study on Hepatocyte-Targeted Phosphorus-31 MRS Using ATP-Loaded Galactosylated Chitosan Oligosaccharide Nanoparticles

机译:ATP负载半乳糖基化壳聚糖寡糖纳米粒子对肝细胞靶向磷31 MRS的初步研究

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Background. The clinical applications of hepatic phosphorus-31 magnetic resonance spectroscopy (31P MRS) remain to be difficult because the changes of phosphates between normal hepatic tissues and pathological tissues are not so obvious, and furthermore, up to now there is few literature on hepatocyte-targeted 31P MRS.Materials and Methods. The ATP-loaded Gal-CSO (Gal-CSO/ATP) nanoparticles were prepared and the special cellular uptake of them as evaluated by using HepG-2 tumor cells and A549 tumor cells, respectively. Two kinds of cells were incubated with the nanoparticles suspension, respectively. Then were prepared the cell samples and the enhancement efficiency of ATP peaks detected by 31P MRS was evaluated.Results. The cellular uptake rate of Gal-CSO/ATP nanoparticles in HepG-2 cells was higher than that in A549 cells. Furthermore, the enlarged ATP peaks of Gal-CSO/ATP nanoparticles in HepG-2 cells were higher than those in A549 cellsin vitrodetected by 31P MRS.Conclusions. Gal-CSO/ATP nanoparticles have significant targeting efficiency in hepatic cellsin vitroand enhancement efficiency of ATP peaks in HepG-2 cells. Furthermore, 31P MRS could be applied in the research of hepatic molecular imaging.
机译:背景。肝磷31磁共振波谱(31P MRS)的临床应用仍然很困难,因为正常肝组织和病理组织之间的磷酸盐变化不那么明显,而且,迄今为止,关于肝细胞靶向的文献很少31P MRS。材料和方法。制备了负载ATP的Gal-CSO(Gal-CSO / ATP)纳米颗粒,并分别通过使用HepG-2肿瘤细胞和A549肿瘤细胞评估了它们的特殊细胞摄取。两种细胞分别与纳米颗粒悬浮液一起孵育。然后制备细胞样品,并评价31P MRS检测到的ATP峰的增强效率。 HepG-2细胞中Gal-CSO / ATP纳米颗粒的细胞摄取率高于A549细胞。 31P MRS体外检测发现,HepG-2细胞中Gal-CSO / ATP纳米颗粒的ATP峰比A549细胞高。 Gal-CSO / ATP纳米粒子在体外肝细胞中具有显着的靶向效率,并且在HepG-2细胞中具有ATP峰的增强效率。此外,31P MRS可用于肝分子成像研究。

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