首页> 外文期刊>Metallomics. integrated biometal science >Elemental bio-imaging of PEGylated NaYF4: Yb/Tm/Gd upconversion nanoparticles in mice by laser ablation inductively coupled plasma mass spectrometry to study toxic side effects on the spleen, liver and kidneys
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Elemental bio-imaging of PEGylated NaYF4: Yb/Tm/Gd upconversion nanoparticles in mice by laser ablation inductively coupled plasma mass spectrometry to study toxic side effects on the spleen, liver and kidneys

机译:通过激光烧蚀电感耦合等离子体质谱法通过激光烧蚀电感耦合等离子体质谱法测定脾脏,肝脏和肾脏毒性副作用

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Rare-earth upconversion nanoparticles (UCNPs) are considered stable nanoprobes with low toxicity and deep tissue penetration. However, the increasing use of UCNPs has raised concerns about their potential toxicity in living organisms. Very few studies have reported the toxicity of UCNPs; hence, it is not possible to conclude yet that UCNPs are safe. In this study, the distribution of PEGylated NaYF4: Yb/Tm/Gd nanoparticles (PEG-UCNPs) in female Balb/c mice following intravenous administration, and imaging in the spleen, liver and kidney was examined by laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS). PEG-UCNPs distributed primarily to the liver and spleen, with significant but lower levels being noted in the kidneys, heart, and lungs. At the sub-organ level, PEG-UCNPs mainly accumulated within the red pulp of the spleen instead of the white pulp, which indicated that PEG-UCNPs are poorly immunogenic, or not immunogenic at all. The imaging of Cu in the liver and spleen showed that the primary clearance organ for PEG-UCNPs is the liver, although they are accumulated in the spleen rather than the liver. This can be explained by the fact that excess superoxide anions produced by phagocytosis of the PEG-UCNPs need Cu-Zn-superoxide dismutase to be converted to hydrogen peroxide. From the Fe, Cu, and Zn imaging of the kidney, it was concluded that PEG-UCNPs do not exhibit nephrotoxicity.
机译:稀土上转化纳米颗粒(UCNPS)被认为是具有低毒性和深层组织渗透的稳定纳米体。然而,UCNP的越来越多的使用提出了对生物体潜在毒性的担忧。很少有研究报告了UCNPS的毒性;因此,不可能得出结论,UCNP是安全的。在该研究中,通过激光烧蚀电感耦合等离子体质谱法检查静脉内给药后雌性BAAYF4:YB / TM / GD纳米粒子(PEG-UCNPS)在静脉内给药后的雌性BALB / C小鼠中的分布,以及在脾脏,肝脏和肾脏中的成像(La-ICP-MS)。 PEG-UCNP主要分布于肝脏和脾脏,在肾脏,心脏和肺部中指出显着但下层水平。在副器官水平,PEG-UCNP主要累积在脾脏的红色纸浆内而不是白色纸浆内,这表明PEG-UCNPS具有较差的免疫原性,或根本不是免疫原性。肝脏和脾脏的Cu的成像表明,PEG-UCNPS的主要间隙器官是肝脏,但它们在脾脏中累积而不是肝脏。这可以通过PEG-UCNPS吞噬作用的过量超氧化物阴离子来解释,PEG-UCNPS产生的超氧化物阴离子需要Cu-Zn-超氧化物歧化酶待转化为过氧化氢。从肾脏的Fe,Cu和Zn成像中,得出结论,PEG-UCNP不会表现出肾毒性。

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