Evaluation of iron oxide nanoparticle micelles for Magnetic Particle Imaging (MPI) of thrombosis

PLoS ONE

Volumn 10, Issue 3, 2015, Pages

  Starmans, Lucas W E ^a   Moonen, Rik P M ^a   Aussems Custers, Erica ^b   Daemen, Mat J A P ^c   Strijkers, Gustav J ^a,c   Nicolay, Klaas ^a   Grüll, Holger ^a,b  

^a EINDHOVEN UNIVERSITY OF TECHNOLOGY   (Netherlands)

^b PHILIPS RESEARCH LABORATORIES   (Netherlands)

^c ACADEMIC MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

CARRIER PROTEINS AND BINDING PROTEINS; FIBRIN BINDING PEPTIDE; IRON OXIDE NANOPARTICLE MICELLE; NANOPARTICLE; UNCLASSIFIED DRUG; FERRIC ION; FERRIC OXIDE; METAL NANOPARTICLE; MICELLE;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BINDING AFFINITY; CAROTID ARTERY THROMBOSIS; CONTROLLED STUDY; CRYOGENIC TRANSMISSION ELECTRON MICROSCOPY; DYNAMIC LIGHT SCATTERING; EX VIVO STUDY; HISTOPATHOLOGY; IMAGE ANALYSIS; IN VIVO STUDY; LIGHT RELATED PHENOMENA; MAGNETIC PARTICLE IMAGING; MAGNETIC PARTICLE SPECTROSCOPY; MOUSE; NANOFABRICATION; NANOIMAGING; NONHUMAN; NUCLEAR MAGNETIC RESONANCE IMAGING; QUANTITATIVE ANALYSIS; SENSITIVITY AND SPECIFICITY; SPECTROSCOPY; TRANSMISSION ELECTRON MICROSCOPY; VALIDATION PROCESS; CHEMISTRY; HUMAN; MICELLE; PROCEDURES; THROMBOSIS;

FERRIC COMPOUNDS; HUMANS; MAGNETIC RESONANCE IMAGING; METAL NANOPARTICLES; MICELLES; THROMBOSIS;

EID: 84929103775     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0119257     Document Type: Article

References (27)

1. Lu Y, Lorenzoni A, Fox JJ, Rademaker J, Els N Vander, Grewal RK, et al. Noncontrast perfusion singlephoton emission CT/CT scanning. Chest. 2014; 145: 1079-1088. doi: 10.1378/chest.13-2090 PMID: 24798835
2. Omran H, Jung W, Rabahieh R, Wirtz P, Becher H, Illien S, et al. Imaging of thrombi and assessment of left atrial appendage function: a prospective study comparing transthoracic and transoesophageal echocardiography. Heart. 1999; 81: 192-198. PMID: 9922358
3. Srichai MB, Junor C, Rodriguez LL, Stillman AE, Grimm RA, Lieber ML, et al. Clinical, imaging, and pathological characteristics of left ventricular thrombus: A comparison of contrast-enhanced magnetic resonance imaging, transthoracic echocardiography, and transesophageal echocardiography with surgical or pathological validation. Am Heart J. 2006; 152: 75-84. doi: 10.1016/j.ahj.2005.08.021 PMID: 16824834
4. Litmanovich D, Bankier AA, Cantin L, Raptopoulos V, Boiselle PM. CT and MRI in diseases of the aorta. Am J Roentgenol. 2009; 193: 928-940. doi: 10.2214/AJR.08.2166 PMID: 19770313
5. Markel A, Weich Y, Gaitini D. Doppler ultrasound in the diagnosis of venous thrombosis. Angiology. 1995; 46: 65-73. doi: 10.1177/000331979504600109 PMID: 7818159
6. Kronzon I. Aortic Atherosclerotic Disease and Stroke. Circulation. 2006; 114: 63-75. doi: 10.1161/CIRCULATIONAHA.105.593418 PMID: 16818829
7. Gleich B, Weizenecker J. Tomographic imaging using the nonlinear response of magnetic particles. Nature. 2005; 435: 1214-7. doi: 10.1038/nature03808 PMID: 15988521
8. Schmitz SA, Winterhalter S, Schiffler S, Gust R, Wagner S, Kresse M, et al. USPIO-enhanced direct MR imaging of thrombus: preclinical evaluation in rabbits. Radiology. 2001; 221: 237-43. doi: 10.1148/radiol.2211001632 PMID: 11568346
9. Kim D-E, Kim J-Y, Sun I-C, Schellingerhout D, Lee S-K, Ahn C-H, et al. Hyperacute direct thrombus imaging using computed tomography and gold nanoparticles. Ann Neurol. 2013; 73: 617-25. doi: 10.1002/ana.23849 PMID: 23495101
10. Starmans LWE, Burdinski D, Haex NPM, Moonen RPM, Strijkers GJ, Nicolay K, et al. Iron Oxide Nano-particle-Micelles (ION-Micelles) for Sensitive (Molecular) Magnetic Particle Imaging and Magnetic Resonance Imaging. PLoS One. 2013; 8: e57335. doi: 10.1371/journal.pone.0057335 PMID: 23437371
11. Weizenecker J, Borgert J, Gleich B. A simulation study on the resolution and sensitivity of magnetic particle imaging. Phys Med Biol. 2007; 52: 6363-74. doi: 10.1088/0031-9155/52/21/001 PMID: 17951848
12. Cengelli F, Maysinger D, Tschudi-Monnet F, Montet X, Corot C, Petri-Fink A, et al. Interaction of functionalized superparamagnetic iron oxide nanoparticles with brain structures. J Pharmacol Exp Ther. 2006; 318: 108-116. doi: 10.1124/jpet.106.101915.micellar PMID: 16608917
13. Chen D-X, Sun N, Gu H-C. Size analysis of carboxydextran coated superparamagnetic iron oxide particles used as contrast agents of magnetic resonance imaging. J Appl Phys. 2009; 106: 063906. doi: 10.1063/1.3211307
14. Biederer S, Knopp T, Sattel TF, Lüdtke-Buzug K, Gleich B, Weizenecker J, et al. Magnetization response spectroscopy of superparamagnetic nanoparticles for magnetic particle imaging. J Phys D Appl Phys. 2009; 42: 205007. doi: 10.1088/0022-3727/42/20/205007
15. Jansen CHP, Perera D, Makowski MR, Wiethoff AJ, Phinikaridou A, Razavi RM, et al. Detection of intracoronary thrombus by magnetic resonance imaging in patients with acute myocardial infarction. Circulation. 2011; 124: 416-424. doi: 10.1161/CIRCULATIONAHA.110.965442 PMID: 21747055
16. Starmans LWE, van Duijnhoven SMJ, Rossin R, Berben M, Aime S, Daemen MJAP, et al. Evaluation of 111In-Labeled EPep and FibPep as Tracers for Fibrin SPECT Imaging. Mol Pharm. 2013; 10: 4309-21. doi: 10.1021/mp400406x PMID: 24099178
17. Wolters M, van Hoof RHM, Wagenaar A, Douma K, van Zandvoort MAMJ, Hackeng TH, et al. MRI artifacts in the ferric chloride thrombus animal model: an alternative solution: preventing MRI artifacts after thrombus induction with a non-ferromagnetic Lewis acid. J Thromb Haemost. 2013; 11: 1766-9. doi: 10.1111/jth.12340 PMID: 23809458
18. Sachs UJH, Nieswandt B. In vivo thrombus formation in murine models. Circ Res. 2007; 100: 979-991. doi: 10.1161/01.RES.0000261936.85776.5f PMID: 17431199
19. Starmans LWE, van Duijnhoven SMJ, Rossin R, Aime S, Daemen MJAP, Nicolay K, et al. SPECT imaging of fibrin using fibrin-binding peptides. Contrast Media Mol Imaging. 2013; 8: 229-37. doi: 10.1002/cmmi.1521 PMID: 23606426
20. Starmans LWE, Kok MB, Sanders HMHF, Zhao Y, Donegá CDM, Meijerink A, et al. Influence of cell-internalization on relaxometric, optical and compositional properties of targeted paramagnetic quantum dot micelles. Contrast Media Mol Imaging. 2011; 6: 100-9. doi: 10.1002/cmmi.411 PMID: 20967880
21. Zhao Y, van Rooy I, Hak S, Fay F, Tang J, Davies CDL, et al. Near-infrared fluorescence energy transfer imaging of nanoparticle accumulation and dissociation kinetics in tumor-bearing mice. ACS Nano. 2013; 7: 10362-70. doi: 10.1021/nn404782p PMID: 24134041
22. Zhao Y, Schapotschnikow P, Skajaa T, Vlugt TJH, Mulder WJM, de Mello Donegá C, et al. Probing lipid coating dynamics of quantum dot core Micelles via Förster resonance energy transfer. Small. 2014; 10: 1163-70. doi: 10.1002/smll.201301962 PMID: 24343988
23. Lundqvist M, Stigler J, Elia G, Lynch I, Cedervall T, Dawson KA. Nanoparticle size and surface properties determine the protein corona with possible implications for biological impacts. Proc Natl Acad Sci U S A. 2008; 105: 14265-14270. doi: 10.1073/pnas.0805135105 PMID: 18809927
24. Salvati A, Pitek AS, Monopoli MP, Prapainop K, Bombelli FB, Hristov DR, et al. Transferrin-functionalized nanoparticles lose their targeting capabilities when a biomolecule corona adsorbs on the surface. Nat Nanotechnol. 2013; 8: 137-43. doi: 10.1038/nnano.2012.237 PMID: 23334168
25. Dai Q, Walkey C, Chan WCW. Polyethylene glycol backfilling mitigates the negative impact of the protein corona on nanoparticle cell targeting. Angew Chemie - Int Ed. 2014; 53: 5093-5096. doi: 10.1002/anie.201309464
26. Van Bochove GS, Sanders HMHF, de Smet M, Keizer HM, Mulder WJM, Krams R, et al. Molecular MR Imaging of Collagen in Mouse Atherosclerosis by Using Paramagnetic CNA35 Micelles. Eur J Inorg Chem. 2012; 2012: 2115-2125. doi: 10.1002/ejic.201200010
27. Coolen BF, Simonis FFJ, Geelen T, Moonen RPM, Arslan F, Paulis LEM, et al. Quantitative T2 mapping of the mouse heart by segmented MLEV phase-cycled T2 preparation. Magn Reson Med. 2014; 72: 409-17. doi: 10.1002/mrm.24952 PMID: 24186703