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Biodistribution and clearance of quantum dots in small animals

机译:小动物中量子点的生物分布和清除

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CdSe-core, ZnS-capped semiconductor nanoparticles - quantum dots (QDs) - have been at the forefront of biomedical nanotechnology research thanks to their unique optical Η photophysical properties. In the present study the impact of the particle coating and size on their in vivo fate after intravenous (IV) injection into mice was studied by fluorescence methods. For this study, we compared organ-selective biodistribution and elimination routes of synthesized QDs coated with 3-mercaptopropionic acid (QD MPA) and commercially available Qtracker 705 nontargeted quantum dots with poly(ethylene glycol) coating (QD PEG). We observed primary accumulation of these QDs in lung. Experiments demonstrated that QD MPA and QD PEG have both remained fluorescent in lung after at least 24 hours postinjection. Moreover, QDs was seen to deposit mainly in liver, spleen, kidney and lymph nodes. We also concluded that QDs MPA and QDs 705 are both sequestered and not excreted with feces or urine.
机译:CdSe核心,ZnS封端的半导体纳米粒子-量子点(QDs)-由于其独特的光学H光物理特性,一直处于生物医学纳米技术研究的前沿。在本研究中,通过荧光方法研究了在静脉内(IV)注入小鼠后颗粒涂层和尺寸对其体内命运的影响。对于本研究,我们比较了涂覆有3-巯基丙酸(QD MPA)的合成QD和具有聚乙二醇涂层(QD PEG)的市售Qtracker 705非靶向量子点的器官选择性生物分布和消除途径。我们观察到这些QD在肺中的初步积累。实验证明,注射后至少24小时后,QD MPA和QD PEG在肺部均保持荧光。此外,人们发现量子点主要沉积在肝,脾,肾和淋巴结中。我们还得出结论,QD MPA和QD 705都是隔离的,不会随粪便或尿液排泄。

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