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1 123I crosstalk into the 99mTc window was 2.79% and was r
2 123I-Ang II formation (as measured by fractional convers
3 123I-Ang metabolites were separated by high-pressure liq
4 123I-Labeled iodoazomycin arabinoside (IAZA) is a marker
5 123I-labeled iodophenylpentadecanoic acid (IPPA) is a sy
6 123I-labeled T84.66 minibodies demonstrated rapid, high
7 [123I] beta-CIT and single photon emission computed tomog
8 [123I]5-iodo-3-[2(S)-2-azetidinylmethoxy]pyridine (5-I-A-
9 sence of systolic thickening (-3.2% +/- 1%), 123I-IPPA defect magnitude (LAD/left circumflex artery [
10 sults of technetium 99m (99mTc)-,iodine 123 (123I)-, and iodine 131 (131I)-labeled anti-CEA antibodie
11 ssing hNIS could be imaged using iodine-123 (123I) and shown to retain iodide for up to 48 hours.
12 y serial gamma-camera imaging of iodine-123 (123I) uptake both in MV-sensitive KAS-6/1 myeloma xenogr
13 tron emission tomography (PET), iodine-123- (123I) and iodine-131 (131I) -metaiodobenzylguanidine (MI
15 ers labeled with 2beta-carbomethoxy-3beta-(4-123I-iodophenyl)tropane (123I-beta-CIT); nine healthy hu
16 The SPECT radioligand, 3-quinuclidinyl-4-[123I]iodobenzilate ([123I]IQNB), binds to muscarinic rec
18 for cortex, regional brain levels of (-)-5-[123I]IBVM ((-)-[123I]5) at 4 h exhibited a linear correl
20 nAChR agonist radiotracer [123I]5-IA-85380 ([123I]5-IA), we imaged beta2*-nAChR availability in human
24 ts to clinicians that a positive (abnormal) [123I]FP-CIT SPECT scan, even in a patient with an EPMS,
25 trial was to assess the use of a fatty acid, 123I-iodophenylpentadecanoic acid (IPPA), to identify vi
28 We studied the feasibility of administering [123I]IBZM as a bolus plus continuous infusion over 8 hr
31 erformed at either 0-7 hr or 18-24 hr after [123I]beta-CIT injection permits calculation of reliable
33 lular range Auger electron emitters 125I and 123I, the thymidine analogue 5-iodo-2'deoxyuridine (IUdR
34 ng using two separate line sources (57Co and 123I); and a set of eight patients with Parkinson's dise
35 iquid chromatography, and 123I-Ang-(1-7) and 123I-Ang II were quantified across the myocardial circul
37 mal and pathologic studies of both 99mTc and 123I activity estimates were very close with ANN to thos
38 ensitive cells in the GI tract for 99mTc and 123I are tenfold lower; those for 131I are fivefold lowe
39 or the simultaneous acquisition of 99mTc and 123I radiotracer distributions in the brain has been dev
42 by high-pressure liquid chromatography, and 123I-Ang-(1-7) and 123I-Ang II were quantified across th
44 Our protocols for imaging both 131I-MIBG and 123I-MIBG, along with the normal distribution of these c
45 istered 99mTc-based radiopharmaceuticals and 123I-Nal, the interval required for urinary levels of ac
46 in brain imaging (11C, 15O, 18F, 99(m)Tc and 123I) and for three radionuclides showing selective upta
49 Therefore, fasting is not necessary before 123I-IPPA SPECT imaging for the assessment of myocardial
50 ding of the D2 radioligand [123I]benzamide ([123I]IBZM) was studied with single photon emission compu
56 time activity curves was used to calculate [123I]-iodobenzovesamicol to vesicular acetylcholine tran
57 purpose of the present study was to compare [123I]-beta-CIT with [123I]-FPCIT in a within-subject des
62 t, in randomized order and on separate days, 123I-IPPA SPECT myocardial imaging under fasting and non
64 The diagnostic yield of planar diagnostic 123I scintigraphy at 24 h was superior to that at 5 h fo
65 and 12 healthy volunteers underwent dynamic [123I]-iodobenzovesamicol SPECT and magnetic resonance (M
66 ectron emitters has antineoplastic effects ([123I]IUdR and [125I]IUdR) in addition to its scintigraph
67 5 min with several concentrations of either [123I]IUdR or [125I]IUdR and their colony survival was me
70 When labeled with the Auger electron emitter 123I or 125I, IUdR demonstrates therapeutic efficacy.
79 nvert 57Co attenuation values into those for 123I, based on a pixel-by-pixel comparison of two coregi
83 controls with a mean of V"3=3.5 and 6.7 for [123I]-beta-CIT (Parkinson's disease and controls, respec
84 8 for [123I]beta-CIT-FP and 7.7 +/- 0.7 for [123I]beta-CIT-FE, showing high in vivo selectivity for t
85 tively) and a mean of V"3=1.34 and 3.70 for [123I]-FPCIT (Parkinson's disease and controls, respectiv
86 cific midbrain activity was 9.1 +/- 1.8 for [123I]beta-CIT-FP and 7.7 +/- 0.7 for [123I]beta-CIT-FE,
92 ithin 30 min, with little or no washout for [123I]beta-CIT-FP and a faster washout for [123I]beta-CIT
93 ional brain levels of (-)-5-[123I]IBVM ((-)-[123I]5) at 4 h exhibited a linear correlation (r2 = 0.99
95 dy was performed to determine differences in 123I image quality at 5 and 24 h for the detection of re
98 and, 3-quinuclidinyl-4-[123I]iodobenzilate ([123I]IQNB), binds to muscarinic receptors and has genera
99 ease, NCT00126425; Meta-Iodobenzylguanidine [123I-mIBG] Scintigraphy Imaging in Patients With Heart F
100 phy and the selective 5-HT2A receptor ligand 123I iodinated 4-amino-N-[1-[3-(4-fluorophenoxy)propyl]-
101 s limited to the most commonly used ligand, [123I]beta-CIT, stratification by affection status dramat
102 l, patients with more symptoms showed lower [123I]IBZM specific binding, consistent with competition
103 med by intravenous injection of 191-226 MBq [123I]5-I-A-85380 and image acquisition for 289-367 min.
109 aged at 24 hr postinjection 222 MBq (6 mCi) [123I]-beta-CIT and serially from 1-6 hr postinjection 33
111 d 52% of the control uptake, while the mean [123I]-FPCIT value for Parkinson's disease patients was 3
113 phenyl)-N-(1-iodoprop-1-en-3-yl)nortropane ([123I]IACFT) for SPECT imaging in an MPTP model of parkin
115 sured 24 hr after the oral administration of 123I, 3.7-7.4 MBq (0.1-0.2 mCi) with no changes in techn
118 thout corrections for cross-contamination of 123I into the 99mTc window, striatum-to-cerebellum ratio
120 hod for nonuniform attenuation correction of 123I emission brain images based on transmission imaging
121 h received a nominal 185-MBq (5 mCi) dose of 123I-IAZA administered as a slow (1-3 min) intravenous i
128 mors (P-1) which showed no in vivo uptake of 123I, NP-1 tumors accumulated 25-30% of the total 123I a
129 In pulmonary emboli, the absolute uptake of 123I-bitistatin (0.64 +/- 0.17% ID/g) was higher than al
131 ing can be complemented by additional use of 123I-labeled D2/D3 receptor ligand co-injected to assess
133 rmed after intra-arterial administration of [123I]IUdR in patients with liver metastases and intraves
134 ne-123 fluoropropyl (FP)CIT is an analog of [123I]-beta-CIT and has been shown to achieve peak tracer
136 ain activity levels, and the application of [123I]IBZM continuous infusion to examine the effects of
137 e healthy male subjects received a bolus of [123I]IBZM followed by a continuous infusion at a bolus (
138 e caused the breakdown of the amide bond of [123I]-31 and rendered this agent obsolete as an in vivo
142 ealthy controls obtained after injection of [123I])beta-CIT in part to assess the utility of this tra
143 measures obtained after bolus injection of [123I]beta-CIT 0-7 hr (Day 1) and 18-24 hr (Day 2) after
144 atio measured at 30 min, after injection of [123I]IACFT was significantly higher (p < 0.01) than with
150 imaging performed at 24 hr postinjection of [123I]beta-CIT permits calculation of reliable and reprod
155 pecificity of scan 89%), the specificity of [123I]FP-CIT SPECT scans was reduced in the FTD group to
158 ale volunteers was measured with the use of [123I] beta-CIT and single photon emission computed tomog
159 IBI (rest and stress), 123I-/124I-/131I-OIH, 123I/131I-NaI, 125I-iothalamate, 111In-DTPA and 89Sr-SrC
161 t 90% of regions that were false negative on 123I-MIBG scintigraphy or [18F]FDA-PET were detected by
163 renic group, elevated amphetamine effect on [123I]IBZM binding potential was associated with emergenc
167 ealthy control subjects participated in one [123I]-beta-CIT and one [123I]-FPCIT SPECT scan separated
168 parison subjects (n=31) participated in one [123I]5-IA-85380 single photon emission computed tomograp
170 56 rats were injected with GdDTPA-albumin or 123I-GdDTPA-albumin either immediately before reperfusio
172 to assess the performance of beta-methyl-p-[123I]-iodophenyl-pentadecanoic acid (BMIPP) single-photo
174 ll five subjects achieved unchanging plasma [123I]IBZM and striatal brain-activity levels over the 30
175 in addition to its scintigraphic potential ([123I]IUdR and [131I]IUdR), it holds promise for therapy
176 ple radioiodination procedure for preparing [123I]IQNB from a tri-n-butylstannyl precursor in a no-ca
177 primary 99mTc image (130-146 keV), a primary 123I image (152-168 keV) and a secondary 99mTc crosstalk
179 Specific binding of the D2 radioligand [123I]benzamide ([123I]IBZM) was studied with single phot
180 mography with the nAChR agonist radiotracer [123I]5-IA-85380 ([123I]5-IA), we imaged beta2*-nAChR ava
181 ial of the specific D2 receptor radiotracer [123I] (S)-(-)-3-iodo-2-hydroxy-6-methoxy-N-[(1-ethyl-2-p
186 ormal and pathologic studies of simultaneous 123I/99mTc brain SPECT when compensating for all degradi
188 yl]tropane (3) with no carrier-added sodium [123I]iodide and hydrogen peroxide in ethanolic HCl.
189 albumin (HSA), 99mTc-MIBI (rest and stress), 123I-/124I-/131I-OIH, 123I/131I-NaI, 125I-iothalamate, 1
190 norepinephrine transporter (NET) substrates [123I]-m-iodobenzylguanidine (MIBG) and [11C]-m-hydroxyep
193 rom striatal tissue 15-20 times faster than [123I]-beta-CIT, and estimates of dopamine transporter lo
196 studies performed in rats demonstrated that [123I]ZIET was selective and specific for SERT-rich regio
198 distribution studies in rats indicated that [123I]ZIET enters the brain readily and accumulates in SE
199 Taken together, the data suggests that [123I]16(IMPY) may be useful for imaging A beta aggregate
201 results showed 1.51% 99mTc crosstalk in the 123I image compared with 12.44% for the uncorrected imag
202 images: results showed 1.3% crosstalk in the 123I image compared with 19.7% for a 10% asymmetric ener
203 ng three experiments with coinjection of the 123I-and 125I-radiolabeled tracer for direct comparison
204 disease biomarkers, brain imaging using the 123I-ioflupane ligand with single-photon emission comput
205 ed from the five control subjects after the [123I]-FPCIT injection for analysis of radiometabolites.
206 16 patients the mean percent decline in the [123I]beta-CIT uptake was significantly greater with levo
210 NP-1 tumors accumulated 25-30% of the total 123I administered with a biological half-life of 45 h.
212 rbomethoxy-3beta-(4-123I-iodophenyl)tropane (123I-beta-CIT); nine healthy human control subjects who
213 -carbomethoxy-3beta-(4-iodophenyl) tropane ([123I]beta-CIT) for measurement of central SERT availabil
215 arboxymethoxy-3 beta-(4-iodophenyl)tropane ([123I]beta-CIT), were used to determine DA transporter de
220 e last 16 yr, thyroid RIU measurements using 123I were obtained in 671 euthyroid patients and 274 hyp
223 nts with bladder carcinoma, initially using [123I]IUdR and currently using both [123I]IUdR and [125I]
224 ity of quantifying alpha4beta2 nAChRs using [123I]5-I-A-85380 and support the use of V(T)' as an appr
225 rters and supports the feasibility of using [123I]beta-CIT in serial evaluation of human neuropsychia
226 jects and supports the feasibility of using [123I]beta-CIT in the evaluation of disease progression i
227 e-photon emission computed tomography using [123I]iodobenzovesamicol (IBVM), an in vivo marker of the
228 eparation of *IUdR by demercuration whereby [123I/125I/131I]IUdR is synthesized virtually instantaneo
231 mpounds could be used as SPECT (labeled with 123I) or PET (labeled with 18F) radiotracers to image th
234 risk area), viability was overestimated with 123I-IPPA, because uptake averaged 64% of normal in the
235 tivity ratios, as is commonly performed with 123I-beta-CIT, these outcome measures showed only small
237 diagnoses, such as Parkinson's disease with (123I)beta-CIT single photon emission computed tomography
239 of beta2*-nAChR binding was conducted with [123I]5-I-A-85380 on prefrontal cortex samples from 14 de
240 These data suggest that SPECT imaging with [123I]-FPCIT visually demonstrates reductions in striatal
241 re is increasing evidence that imaging with [123I]FP-CIT SPECT is helpful in differentiating dementia
242 ts of SPECT and delayed planar imaging with [123I]MIBG in neuroblastoma have not yet been fully estab
243 Four healthy volunteers were injected with [123I]-beta-CIT-FP and another four were injected with [1
246 residual nicotine would not interfere with [123I]5-IA binding to the beta2*-nAChR as approximately 7
247 d decline in striatal uptake was noted with [123I] beta CIT-FP (r = -0.56, p < 0.04) but not with [18
248 inetics, and the good results obtained with [123I]ZIET in rats support the candidacy of [11C]ZIET for
249 sympathetic innervation and perfusion with [123I]metaiodobenzylguanidine (MIBG) and 201Tl, respectiv
251 emission computed tomography scanning with [123I]2beta-carbomethoxy-3beta-(4-iodophenyl) tropane ([1
252 seven patients underwent scintigraphy with [123I]meta-iodobenzylguanidine (MIBG), and two patients w
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