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评估超小超顺磁性氧化铁纳米颗粒用于长期磁性细胞标记的效果。

Evaluating the effect of ultrasmall superparamagnetic iron oxide nanoparticles for a long-term magnetic cell labeling.

作者信息

Shanehsazzadeh Saeed, Oghabian Mohammad Ali, Allen Barry J, Amanlou Massoud, Masoudi Afshin, Daha Fariba Johari

机构信息

Department of Medical Physics and Biomedical Engineering, Faculty of Medicine, Tehran, Iran.

出版信息

J Med Phys. 2013 Jan;38(1):34-40. doi: 10.4103/0971-6203.106603.

DOI:10.4103/0971-6203.106603
PMID:23531682
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3607343/
Abstract

In order to evaluate the long-term viability, the iron content stability, and the labeling efficiency of mammalian cells using magnetic cell labeling; dextran-coated ultrasmall superparamagnetic iron oxide (USPIOs) nanoparticles with plain surfaces having a hydrodynamic size of 25 nm were used for this study. Tests were carried out in four groups each containing 5 flasks of 5.5 × 10(6) AD-293 embryonic kidney cells. The cell lines were incubated for 24 h using four different iron concentrations with and without protamine sulfate (Pro), washed with phosphate-buffered saline (PBS) and centrifuged three times to remove the unbounded USPIOs. Cell viability was also verified using USPIOs. There were no significant differences in the cell viability between the control group of cells and those groups with iron uptake at the specified iron concentrations. The average iron uptake ratio compared to that of the control group was (114 ± 1). The magnetic resonance images (MRI) at post-labeling day 1 and day 21 showed (75 ± 4)% and (22 ± 5)% signal decrements compared to that of the control, respectively. The Perl's Prussian blue test showed that 98% of the cells were labeled, and the iron concentration within the media did not affect the cell iron uptake. Magnetic cellular labeling with the USPIO-Pro complex had no short or medium term (3 weeks) toxic effects on AD-293 embryonic kidney cells.

摘要

为了评估使用磁性细胞标记法的哺乳动物细胞的长期活力、铁含量稳定性和标记效率;本研究使用了具有25nm流体动力学尺寸的表面平整的葡聚糖包被超小超顺磁性氧化铁(USPIOs)纳米颗粒。实验在四组中进行,每组包含5个装有5.5×10(6)个AD - 293胚胎肾细胞的培养瓶。细胞系使用四种不同铁浓度并分别添加和不添加硫酸鱼精蛋白(Pro)孵育24小时,用磷酸盐缓冲盐水(PBS)洗涤并离心三次以去除未结合的USPIOs。还使用USPIOs验证了细胞活力。在指定铁浓度下,对照组细胞与摄取铁的组之间的细胞活力没有显著差异。与对照组相比,平均铁摄取率为(114±1)。标记后第1天和第21天的磁共振图像(MRI)显示,与对照组相比,信号分别降低了(75±4)%和(22±5)%。Perl普鲁士蓝试验表明98%的细胞被标记,并且培养基中的铁浓度不影响细胞对铁的摄取。用USPIO - Pro复合物进行磁性细胞标记对AD - 293胚胎肾细胞没有短期或中期(3周)毒性作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dad/3607343/b4f227c0d179/JMP-38-34-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dad/3607343/434aa9a78ccf/JMP-38-34-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dad/3607343/5082c964e6d5/JMP-38-34-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dad/3607343/6d59c7739497/JMP-38-34-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dad/3607343/e50904c22d9b/JMP-38-34-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dad/3607343/2aa34d2f4d70/JMP-38-34-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dad/3607343/b4f227c0d179/JMP-38-34-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dad/3607343/434aa9a78ccf/JMP-38-34-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dad/3607343/5082c964e6d5/JMP-38-34-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dad/3607343/6d59c7739497/JMP-38-34-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dad/3607343/e50904c22d9b/JMP-38-34-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dad/3607343/2aa34d2f4d70/JMP-38-34-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dad/3607343/b4f227c0d179/JMP-38-34-g008.jpg

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