Comparison of electron spin resonance spectroscopy and inductively-coupled plasma optical emission spectroscopy for biodistribution analysis of iron-oxide nanoparticles.
Comparison of electron spin resonance spectroscopy and inductively-coupled plasma optical emission spectroscopy for biodistribution analysis of iron-oxide nanoparticles.
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DOI:
10.1021/mp900161h
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发表时间:
2010-04-05
影响因子:
4.9
通讯作者:
Yang VC
中科院分区:
文献类型:
--
作者:
Chertok B;Cole AJ;David AE;Yang VC
Magnetic nanoparticles (MNP) have been widely studied for use in targeted drug delivery. Analysis of MNP biodistribution is essential to evaluating the success of targeting strategies and the potential for off-target toxicity. This work compared the applicability of inductively-coupled plasma optical emission spectroscopy (ICP-OES) and electron spin resonance (ESR) spectroscopy in assessing MNP biodistribution. Biodistribution was evaluated in 9L-glioma bearing rats administered with MNP (12-25 mg Fe/kg) under magnetic targeting. Ex vivo analysis of MNP in animal tissues was performed with both ICP-OES and ESR. A cryogenic method was developed to overcome the technical hurdle of loading tissue samples into ESR tubes. Comparison of results from the ICP-OES and ESR measurements revealed two distinct relationships for organs accumulating high or low levels of MNP. In organs with high MNP accumulation such as liver and spleen, data were strongly correlated (r = 0.97, 0.94 for liver and spleen, respectively), thus validating equivalency of the two methods in this high concentration range (> 1000 nmol Fe/g tissue). The two sets of measurements, however, differed significantly in organs with lower levels of MNP accumulation such as brain, kidney, and the tumor. Whereas ESR resolved MNP to 10-55 nmol Fe/g tissue, ICP-OES failed to detect MNP due to masking by endogenous iron. These findings suggest that ESR coupled to cryogenic sample handling is more robust than ICP-OES, attaining better sensitivity in analyses. Such advantages render ESR the method of choice for accurate profiling of MNP biodistribution across tissues with high variability in nanoparticle accumulation.
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影响因子:
5
作者:
MARCHAL, G;VANHECKE, P;VANDERSCHUEREN, E
通讯作者:
VANDERSCHUEREN, E
影响因子:
3.9
作者:
Jordan, A;Scholz, R;Felix, R
通讯作者:
Felix, R
DOI:
10.1016/j.bbrc.2008.06.126
发表时间:
2008-09-19
影响因子:
3.1
作者:
Kou, Geng;Wang, Shuhui;Guo, Yajun
通讯作者:
Guo, Yajun
影响因子:
2.7
作者:
Lazaro, Francisco Jose;Gutierrez, Lucia;Munoz, Maria Jesus
通讯作者:
Munoz, Maria Jesus
影响因子:
2.7
作者:
Mykhaylyk, O;Dudchenko, N;Dudchenko, A
通讯作者:
Dudchenko, A