Evaluation of 99Tcm-bicisate as a renal imaging agent

Tc-bicisate (Tc-ECD), often used as a brain perfusion agent, is rapidly converted following intravenous injection to the polar monoacid (Tc-ECM) and diacid (Tc-EC) metabolites. Such polar metabolites, which are eliminated principally by renal clearance, are potential renal imaging agents. In this st...

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Veröffentlicht in:Nuclear medicine communications 1997-08, Vol.18 (8), p.771-775
Hauptverfasser: OZKER, K, KABASAKAL, L, LIU, Y, HELLMAN, R S, ISITMAN, A, KRASNOW, A Z, COLLIER, B D
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container_end_page 775
container_issue 8
container_start_page 771
container_title Nuclear medicine communications
container_volume 18
creator OZKER, K
KABASAKAL, L
LIU, Y
HELLMAN, R S
ISITMAN, A
KRASNOW, A Z
COLLIER, B D
description Tc-bicisate (Tc-ECD), often used as a brain perfusion agent, is rapidly converted following intravenous injection to the polar monoacid (Tc-ECM) and diacid (Tc-EC) metabolites. Such polar metabolites, which are eliminated principally by renal clearance, are potential renal imaging agents. In this study, Tc-ECD was compared for the first time with Tc-EC, Tc-mercaptoacetyltriglycine (Tc-MAG3) and I-orthoiodohippurate (OIH) as renal imaging agents in rabbits. Whole-body images and renograms were obtained for all three of the Tc agents, and pharmacokinetic parameters including plasma and urinary clearance were studied for all four agents. The plasma clearance of Tc-EC (37 ml min) was slower than that of Tc-ECD (51 ml min), which could be accounted for by the higher liver uptake of Tc-ECD. The urinary clearance of Tc-ECD (35 ml min), Tc-EC (34 ml min) and Tc-MAG3 (39 ml min) was similar. The renal images obtained with Tc-ECD were comparable to those for Tc-MAG3 and Tc-EC. However, liver uptake was more prominent with Tc-ECD than with the other agents. The Tc-ECD renogram curves showed a prolonged decrease in renal activity compared to both Tc-EC and Tc-MAG3. In potential human studies, the relatively high liver uptake of Tc-ECD superimposed on right renal activity may be a limitation. Therefore, we conclude that Tc-ECD is less favourable when compared to existing renal agents due to its high extrarenal uptake and renal kinetics.
doi_str_mv 10.1097/00006231-199708000-00011
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Such polar metabolites, which are eliminated principally by renal clearance, are potential renal imaging agents. In this study, Tc-ECD was compared for the first time with Tc-EC, Tc-mercaptoacetyltriglycine (Tc-MAG3) and I-orthoiodohippurate (OIH) as renal imaging agents in rabbits. Whole-body images and renograms were obtained for all three of the Tc agents, and pharmacokinetic parameters including plasma and urinary clearance were studied for all four agents. The plasma clearance of Tc-EC (37 ml min) was slower than that of Tc-ECD (51 ml min), which could be accounted for by the higher liver uptake of Tc-ECD. The urinary clearance of Tc-ECD (35 ml min), Tc-EC (34 ml min) and Tc-MAG3 (39 ml min) was similar. The renal images obtained with Tc-ECD were comparable to those for Tc-MAG3 and Tc-EC. However, liver uptake was more prominent with Tc-ECD than with the other agents. The Tc-ECD renogram curves showed a prolonged decrease in renal activity compared to both Tc-EC and Tc-MAG3. 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Such polar metabolites, which are eliminated principally by renal clearance, are potential renal imaging agents. In this study, Tc-ECD was compared for the first time with Tc-EC, Tc-mercaptoacetyltriglycine (Tc-MAG3) and I-orthoiodohippurate (OIH) as renal imaging agents in rabbits. Whole-body images and renograms were obtained for all three of the Tc agents, and pharmacokinetic parameters including plasma and urinary clearance were studied for all four agents. The plasma clearance of Tc-EC (37 ml min) was slower than that of Tc-ECD (51 ml min), which could be accounted for by the higher liver uptake of Tc-ECD. The urinary clearance of Tc-ECD (35 ml min), Tc-EC (34 ml min) and Tc-MAG3 (39 ml min) was similar. The renal images obtained with Tc-ECD were comparable to those for Tc-MAG3 and Tc-EC. However, liver uptake was more prominent with Tc-ECD than with the other agents. The Tc-ECD renogram curves showed a prolonged decrease in renal activity compared to both Tc-EC and Tc-MAG3. 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Radiopharmaceuticals</subject><subject>Cysteine - analogs &amp; derivatives</subject><subject>Cysteine - pharmacokinetics</subject><subject>Humans</subject><subject>Investigative techniques, diagnostic techniques (general aspects)</subject><subject>Iodine Radioisotopes - pharmacokinetics</subject><subject>Iodohippuric Acid - pharmacokinetics</subject><subject>Kidney - diagnostic imaging</subject><subject>Kidney - metabolism</subject><subject>Medical sciences</subject><subject>Metabolic Clearance Rate</subject><subject>Organotechnetium Compounds - pharmacokinetics</subject><subject>Pharmacology. 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Radiopharmaceuticals</topic><topic>Cysteine - analogs &amp; derivatives</topic><topic>Cysteine - pharmacokinetics</topic><topic>Humans</topic><topic>Investigative techniques, diagnostic techniques (general aspects)</topic><topic>Iodine Radioisotopes - pharmacokinetics</topic><topic>Iodohippuric Acid - pharmacokinetics</topic><topic>Kidney - diagnostic imaging</topic><topic>Kidney - metabolism</topic><topic>Medical sciences</topic><topic>Metabolic Clearance Rate</topic><topic>Organotechnetium Compounds - pharmacokinetics</topic><topic>Pharmacology. Drug treatments</topic><topic>Rabbits</topic><topic>Radionuclide Imaging</topic><topic>Radionuclide investigations</topic><topic>Radiopharmaceuticals - pharmacokinetics</topic><topic>Technetium Tc 99m Mertiatide - pharmacokinetics</topic><topic>Urinary system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>OZKER, K</creatorcontrib><creatorcontrib>KABASAKAL, L</creatorcontrib><creatorcontrib>LIU, Y</creatorcontrib><creatorcontrib>HELLMAN, R S</creatorcontrib><creatorcontrib>ISITMAN, A</creatorcontrib><creatorcontrib>KRASNOW, A Z</creatorcontrib><creatorcontrib>COLLIER, B D</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Nuclear medicine communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>OZKER, K</au><au>KABASAKAL, L</au><au>LIU, Y</au><au>HELLMAN, R S</au><au>ISITMAN, A</au><au>KRASNOW, A Z</au><au>COLLIER, B D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evaluation of 99Tcm-bicisate as a renal imaging agent</atitle><jtitle>Nuclear medicine communications</jtitle><addtitle>Nucl Med Commun</addtitle><date>1997-08</date><risdate>1997</risdate><volume>18</volume><issue>8</issue><spage>771</spage><epage>775</epage><pages>771-775</pages><issn>0143-3636</issn><eissn>1473-5628</eissn><abstract>Tc-bicisate (Tc-ECD), often used as a brain perfusion agent, is rapidly converted following intravenous injection to the polar monoacid (Tc-ECM) and diacid (Tc-EC) metabolites. Such polar metabolites, which are eliminated principally by renal clearance, are potential renal imaging agents. In this study, Tc-ECD was compared for the first time with Tc-EC, Tc-mercaptoacetyltriglycine (Tc-MAG3) and I-orthoiodohippurate (OIH) as renal imaging agents in rabbits. Whole-body images and renograms were obtained for all three of the Tc agents, and pharmacokinetic parameters including plasma and urinary clearance were studied for all four agents. The plasma clearance of Tc-EC (37 ml min) was slower than that of Tc-ECD (51 ml min), which could be accounted for by the higher liver uptake of Tc-ECD. The urinary clearance of Tc-ECD (35 ml min), Tc-EC (34 ml min) and Tc-MAG3 (39 ml min) was similar. The renal images obtained with Tc-ECD were comparable to those for Tc-MAG3 and Tc-EC. However, liver uptake was more prominent with Tc-ECD than with the other agents. The Tc-ECD renogram curves showed a prolonged decrease in renal activity compared to both Tc-EC and Tc-MAG3. In potential human studies, the relatively high liver uptake of Tc-ECD superimposed on right renal activity may be a limitation. Therefore, we conclude that Tc-ECD is less favourable when compared to existing renal agents due to its high extrarenal uptake and renal kinetics.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott-Raven Publishers</pub><pmid>9293508</pmid><doi>10.1097/00006231-199708000-00011</doi><tpages>5</tpages></addata></record>
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source MEDLINE; Journals@Ovid Ovid Autoload
subjects Animals
Biological and medical sciences
Biotransformation
Contrast media. Radiopharmaceuticals
Cysteine - analogs & derivatives
Cysteine - pharmacokinetics
Humans
Investigative techniques, diagnostic techniques (general aspects)
Iodine Radioisotopes - pharmacokinetics
Iodohippuric Acid - pharmacokinetics
Kidney - diagnostic imaging
Kidney - metabolism
Medical sciences
Metabolic Clearance Rate
Organotechnetium Compounds - pharmacokinetics
Pharmacology. Drug treatments
Rabbits
Radionuclide Imaging
Radionuclide investigations
Radiopharmaceuticals - pharmacokinetics
Technetium Tc 99m Mertiatide - pharmacokinetics
Urinary system
title Evaluation of 99Tcm-bicisate as a renal imaging agent
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