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In vivo pharmacokinetics, long-term biodistribution and toxicology study of functionalized upconversion nanoparticles in mice

机译:小鼠功能化上转换纳米粒子的体内药代动力学,长期生物分布和毒理学研究

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Aims: We investigated the in vivo pharmacokinetics, long-term biodistribution and toxicology of polymer-coated upconversion nanoparticles (UCNPs) in mice. Materials & Methods: Near infrared emitting Yb3+/Tm3+-doped NaYF4 UCNPs coated with either polyethylene glycol (PEG) or polyacrylic acid (PAA) were intravenously injected into mice. Blood levels of UCNPs were measured. Yttrium levels in various organs were measured to determine the biodistribution of UCNPs over 3 months. Serum biochemistry, hematology and histology assays were conducted for in vivo toxicology assays. Results: UCNP-PEG exhibited improved stability in physiological solutions and prolonged blood circulation half-lives more than UCNP-PAA. No noticeable toxic side effect was noticed for either UCNP-PAA or UCNP-PEG in our toxicology study, despite the long-term retention of those nanoparticles in the reticuloendothelial systems including the liver and spleen of mice. Conclusion: Although more systematic investigations are still required, the absence of appreciable toxicity shown in our study encourages future explorations of UCNPs for in vivo biomedical applications. Revised submitted: 29/10/2010; Revised submitted: 19/02/2011
机译:目的:我们研究了聚合物包覆的上转换纳米颗粒(UCNPs)在小鼠体内的体内药代动力学,长期生物分布和毒理学。材料与方法:涂有聚乙二醇(PEG)或聚丙烯酸酯的近红外发射Yb 3 + / Tm 3 + 掺杂的NaYF 4 UCNP酸(PAA)被静脉注射到小鼠体内。测量了UCNP的血液水平。测量了各个器官中的钇水平,以确定3个月内UCNP的生物分布。进行血清生物化学,血液学和组织学测定以用于体内毒理学测定。结果:UCNP-PEG在生理溶液中的稳定性得到改善,并且血液循环半衰期比UCNP-PAA长。在我们的毒理学研究中,尽管UCNP-PAA或UCNP-PEG都没有明显的毒性副作用,尽管这些纳米颗粒长期保留在网状内皮系统(包括小鼠的肝脏和脾脏)中。结论:尽管仍需要进行更系统的研究,但我们研究中显示的明显毒性的缺乏鼓励了对UCNPs在体内生物医学应用中的进一步探索。提交的修订日期:2010年10月29日;修改的提交时间:2011年2月19日

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