» Articles » PMID: 18574049

In Vivo Monitoring of Inflammation After Cardiac and Cerebral Ischemia by Fluorine Magnetic Resonance Imaging

Overview
Journal Circulation
Date 2008 Jun 25
PMID 18574049
Citations 141
Authors
Affiliations
Soon will be listed here.
Abstract

Background: In this study, we developed and validated a new approach for in vivo visualization of inflammatory processes by magnetic resonance imaging using biochemically inert nanoemulsions of perfluorocarbons (PFCs).

Methods And Results: Local inflammation was provoked in 2 separate murine models of acute cardiac and cerebral ischemia, followed by intravenous injection of PFCs. Simultaneous acquisition of morphologically matching proton ((1)H) and fluorine ((19)F) images enabled an exact anatomic localization of PFCs after application. Repetitive (1)H/(19)F magnetic resonance imaging at 9.4 T revealed a time-dependent infiltration of injected PFCs into the border zone of infarcted areas in both injury models, and histology demonstrated a colocalization of PFCs with cells of the monocyte/macrophage system. We regularly found the accumulation of PFCs in lymph nodes. Using rhodamine-labeled PFCs, we identified circulating monocytes/macrophages as the main cell fraction taking up injected nanoparticles.

Conclusions: PFCs can serve as a "positive" contrast agent for the detection of inflammation by magnetic resonance imaging, permitting a spatial resolution close to the anatomic (1)H image and an excellent degree of specificity resulting from the lack of any (19)F background. Because PFCs are nontoxic, this approach may have a broad application in the imaging and diagnosis of numerous inflammatory disease states.

Citing Articles

CD63 as novel target for nanoemulsion-based F MRI imaging and drug delivery to activated cardiac fibroblasts.

Euan Martinez A, Bergmann A, Tellkamp F, Schott-Verdugo S, Bouvain P, Steinhausen J Theranostics. 2025; 15(1):1-18.

PMID: 39744226 PMC: 11667234. DOI: 10.7150/thno.96990.


Design of a Robust Flow Cytometric Approach for Phenotypical and Functional Analysis of Human Monocyte Subsets in Health and Disease.

Ahrazoglu T, Kluczny J, Kleimann P, Irschfeld L, Nienhaus F, Bonner F Biomolecules. 2024; 14(10).

PMID: 39456184 PMC: 11506830. DOI: 10.3390/biom14101251.


MRI detection of free-contrast agent nanoparticles.

Garello F, Cavallari E, Capozza M, Ribodino M, Parolisi R, Buffo A Magn Reson Med. 2024; 93(2):761-774.

PMID: 39344270 PMC: 11604830. DOI: 10.1002/mrm.30292.


Combined ROS Sensitive PEG-PPS-PEG with Peptide Agonist for Effective Target Therapy in Mouse Model.

Xiang P, Liu Q, Jing W, Wang Y, Yu H Int J Nanomedicine. 2024; 19:9109-9120.

PMID: 39253061 PMC: 11382658. DOI: 10.2147/IJN.S471036.


Non-invasive mapping of systemic neutrophil dynamics upon cardiovascular injury.

Bouvain P, Ding Z, Kadir S, Kleimann P, Kluge N, Tiren Z Nat Cardiovasc Res. 2024; 2(2):126-143.

PMID: 39196054 PMC: 11357992. DOI: 10.1038/s44161-022-00210-w.


References
1.
Jaffer F, Sosnovik D, Nahrendorf M, Weissleder R . Molecular imaging of myocardial infarction. J Mol Cell Cardiol. 2006; 41(6):921-33. DOI: 10.1016/j.yjmcc.2006.09.008. View

2.
Jander S, Schroeter M, Saleh A . Imaging inflammation in acute brain ischemia. Stroke. 2007; 38(2 Suppl):642-5. DOI: 10.1161/01.STR.0000250048.42916.ad. View

3.
Smith D, Kornbrust E, Lane T . Phagocytosis of a fluorescently labeled perflubron emulsion by a human monocyte cell line. Artif Cells Blood Substit Immobil Biotechnol. 1994; 22(4):1215-21. DOI: 10.3109/10731199409138818. View

4.
Yu J, Kodibagkar V, Cui W, Mason R . 19F: a versatile reporter for non-invasive physiology and pharmacology using magnetic resonance. Curr Med Chem. 2005; 12(7):819-48. DOI: 10.2174/0929867053507342. View

5.
Sze G, Bravo S, Baierl P, SHIMKIN P . Developing spinal column: gadolinium-enhanced MR imaging. Radiology. 1991; 180(2):497-502. DOI: 10.1148/radiology.180.2.2068319. View