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Pharmacokinetics of the three radioiodinated dopamine D2 receptor ligands [123I]IBF, [123I]epidepride and [123I]2′-ISP in nonhuman primates

✍ Scribed by Baldwin, Ronald M.; Zea-Ponce, Yolanda; Zoghbi, Sami S.; Al-Tikriti, Mohammed S.; Seibyl, John P.; Sybirska, Elzbieta H.; Malison, Robert T.; Laruelle, Marc; Charney, Dennis S.; Hoffer, Paul B.


Book ID
123580486
Publisher
Elsevier Science
Year
1994
Tongue
English
Weight
902 KB
Volume
21
Category
Article
ISSN
0969-8051

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📜 SIMILAR VOLUMES


Preparation of [123I]- and [125I]epidepr
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## Abstract (__S__)‐(−)‐__N__‐[(1‐ethyl‐2‐pyrrolidinyl)methyl]‐5‐[^123^I]iodo‐2,3‐dimethoxybenzamide (TDP 517) (proposed generic name, [^123^I]epidepride) is the iodine‐123 substituted analogue of isoremoxipride (FLB 457), both of which are very potent dopamine D‐2 antagonists (epidepride K~D~ 0.02

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Quantitative SPECT measures of dopamine D 2 like receptors with [ 123 I]epidepride is complicated by its high affinity and lipophilic metabolites. The purpose of this study was to use both parent (P) and lipophilic metabolites (M) as input functions in a kinetic paradigm and in comparison to the res

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## Abstract We used the reversibly binding D2 dopamine receptor radioligand [^123^I]IBZM (iodobenzamide) to test whether the endogenous neurotransmitter dopamine competes in vivo for radiotracer binding measured with single photon emission computed tomography (SPECT). In a series of nonhuman primat