Review Article

Radiopharmaceutical Stem Cell Tracking for Neurological Diseases

Table 1

Preclinical studies using radiopharmaceuticals for stem cell tracking in neurology.

Study referenceRadiopharmaceuticalModelAnimalsCell typeRouteTime from lesionNumber of treated animals (number of controls)Number of cells injectedInfusion volume, rate, and durationImaging time points

de Haro et al., 2005 [19] In-oxineSpinal cord injury at T8-T10Wistar ratsRat BM-MSCsTail vein or intralesional3 months20 (no controls) 0.1 or 1 mL3–10 days
Mäkinen et al., 2006 [20] In-oxineTransient MCAO
(120 minutes)
Wistar ratsHuman UCB-MNCsFemoral vein24 hNot specified 0.5 mL0 and 24 h
Lappalainen et al., 2008 [21] In-oxineTransient MCAO
(120 minutes)
Wistar ratsHuman ES-NPCs or rat HPCsCommon carotid artery or femoral vein24 h13 (controls not specified) 0.5 mL0 and 24 h
Lo et al., 2008 [22] I-FIAUSpinal cord injury at T10Long-Evans ratsMouse embryo-derived fibroblastsSpinal cord at L1 level0 h20 (no controls) 0.5 mL 2, 24 and 48 h
Detante et al., 2009 [23] Tc-HMPAOTransient MCAO
(90 minutes)
Sprague-Dawley ratsHuman BM-MSCsSaphenous vein7 days9 (9 controls) 1 mL2 and 20 h
Yoon et al., 2010 [24] In-oxineTraumatic brain injurySprague-Dawley ratsRat BM-MSCsTail vein24 h 3 (2 controls) 1 mL24 h
Park et al., 2011 [25] Tc-HMPAOTraumatic brain injurySprague-Dawley ratsRat BM-MSCsTail veinNot specified14 (13 controls) 1 mL4 h
Vasconcelos-dos-Santos et al., 2012 [26] TcPermanent thermocoagulation of pial blood vesselsWistar ratsHuman BM-MNCsCommon carotid artery or jugular vein24 h12 (8 controls) 0.5 mL 2 and 24 h
Arbab et al., 2012 [27] In-oxineTransient MCAO
(120 minutes)
Wistar ratsHuman UTCsTail vein48 h13 (12 controls) 2 mL 0, 1, and 3 days
Mitkari et al., 2013 [28] In-oxineTransient MCAO
(90 minutes)
Wistar ratsHuman BM-MSCsExternal carotid artery24 h19 (controls not specified) 0.5 mL30 minutes
and 24 h
Gubert et al., 2013 [29] TcPermanent bilateral common carotid ligationLister hooded ratsRat BM-MNCsTail vein24 h23 (no controls) 0.4 mL1 h
Goldmacher et al., 2013 [30] In-oxineTransient MCAO
(120 minutes)
Sprague-Dawley ratsRat BM-MSCsTail vein24 h3 (3 controls) 0.5 mL4, 20, 44, and
70 h
Makela et al., 2013 [31] Tc-HMPAOTransient brachiocephalic trunk and subclavian artery occlusion (7 minutes)PigsPig BM-MNCsBrachiocephalic trunk24 h10 (no controls) Not specified2, 4, 6, 12, and
24 h
Manley et al., 2013 [32] Tc-HMPAOTransient MCAO
(60 minutes)
Sprague-Dawley ratsRat BM-DCsCarotid artery3 h4 (no controls) 0.3 mL/0.1 mL/min5–20 minutes
and 5-6 h
Ramos et al., 2013 [33] TcPermanent vertebral occlusion and transient carotid artery occlusion (17 minutes)Wistar ratsRat BM-MNCsCommon carotid artery24 or 72 h4 (5 controls) 0.3 mL2 h
Wu et al., 2013 [34] I-FIAUTransient MCAO
(60 minutes)
Sprague-Dawley ratsRat BM-MSCsIntracerebral, intraventricular, carotid artery or tail vein24 h20 (4 controls) 15 μL (intracerebral and intraventricular) or 0.5 mL (carotid artery or tail vein)2, 8, and 24 h
Guan et al., 2013 [35] F-FDGTraumatic brain injurySprague-Dawley ratsHuman BM-MSCs and/or collagen scaffoldIntracerebral7 days9 (MSCs); 9 (MSCs + collagen) 0.2 mL3, 6, and 12 h

In-oxine: indium-111-oxine; I-FIAU: iodine-131-2′-fluoro-2′-deoxy-1- D-arabinofuranosyl-5-iodouracil; F-FDG: fluorine-18-fluorodeoxyglucose; Tc: technetium-99m; Tc-HMPAO: technetium-99m-hexamethylpropyleneamine oxime; BM-DCs: bone marrow-derived dendritic cells; BM-MNCs: bone marrow mononuclear cells; BM-MSCs: bone marrow-derived mesenchymal stem cells; EPCs: endothelial progenitor cells; ES-NPCs: embryonic stem cell-derived neural progenitor cells; HPCs: hippocampal progenitor cells; MCAO: middle cerebral artery occlusion; UCB-MNCs: umbilical cord blood mononuclear cells; UTCs: umbilical tissue-derived cells.