Biodistribution and pharmacokinetic studies of SPION using particle electron paramagnetic resonance, MRI and ICP-MS

被引:29
作者
Gobbo, Oliviero L. [1 ,2 ]
Wetterling, Friedrich [2 ]
Vaes, Peter [3 ]
Teughels, Stephanie [3 ]
Markos, Farouk [4 ]
Edge, Deirdre [4 ]
Shortt, Christine M. [4 ]
Crosbie-Staunton, Kieran [5 ]
Radomski, Marek W. [1 ]
Volkov, Yuri [5 ,6 ]
Prina-Mello, Adriele [5 ,6 ]
机构
[1] Sch Pharm & Pharmaceut Sci, Dublin, Ireland
[2] Univ Dublin Trinity Coll, Inst Neurosci, Dublin 2, Ireland
[3] PEPRIC NV, Leuven, Belgium
[4] Natl Univ Ireland Univ Coll Cork, Dept Physiol, Cork, Ireland
[5] Sch Med, Dublin, Ireland
[6] Univ Dublin Trinity Coll, CRANN, Dublin 2, Ireland
关键词
biodistribution; ICP-MS; MRI; nanomedicine; pEPR; pharmacokinetics; SPION; MAGNETIC NANOPARTICLES; MANGANESE; AGENTS;
D O I
10.2217/nnm.15.22
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Aim: Superparamagnetic iron oxide nanoparticles (SPIONs) may play an important role in nanomedicine by serving as drug carriers and imaging agents. In this study, we present the biodistribution and pharmacokinetic properties of SPIONs using a new detection method, particle electron paramagnetic resonance (pEPR). Materials & methods: The pEPR technique is based on a low-field and low-frequency electron paramagnetic resonance. pEPR was compared with inductively coupled plasma mass spectrometry and MRI, in in vitro and in vivo. Results: The pEPR, inductively coupled plasma mass spectrometry and MRI results showed a good correlation between the techniques. Conclusion: The results indicate that pEPR can be used to detect SPIONs in both preclinical and clinical studies.
引用
收藏
页码:1751 / 1760
页数:10
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