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Predicate | Object |
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rdf:type | |
lifeskim:mentions |
umls-concept:C0004927,
umls-concept:C0013682,
umls-concept:C0023779,
umls-concept:C0032521,
umls-concept:C0205148,
umls-concept:C0332256,
umls-concept:C0456205,
umls-concept:C0456603,
umls-concept:C1167624,
umls-concept:C1280500,
umls-concept:C1548779,
umls-concept:C1550605,
umls-concept:C1622418,
umls-concept:C1664784,
umls-concept:C1947902,
umls-concept:C2827499
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pubmed:issue |
1
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pubmed:dateCreated |
1997-9-25
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pubmed:abstractText |
When injected intravenously, lipid vesicles labeled with 99mTc by means of a lipophilic chelator dipalmitoylphosphatidylethanolamine-diethylenetriaminetetraacetic acid (PE-DTTA) are rapidly accumulated by the mononuclear phagocytic system (MPS). By derivatizing the membrane surface with the lipid-polymer complex dipalmitoylphosphatidylethanolamine-monomethoxy polyethylene glycol 5000 (PE-MPEG), MPS uptake can be suppressed and loss of 99mTc label from the lipid surface reduced depending upon both PE-DTTA and PE-MPEG content. For vesicles containing 20% PE-DTTA, addition of PE-MPEG makes no difference to their rate of clearance from the circulation. However for vesicles containing 2% PE-DTTA, addition of more than 0.8% PE-MPEG increases circulation half-life, suppresses liver uptake and reduces renal clearance of the 99mTc label. The molar ratio of reducing agent (Sn) to chelator (PE-DTTA) is critical to efficient and reproducible labeling. For vesicles containing 2% PE-DTTA at a lipid concentration of 100 mM, a Sn/DTTA ratio of 0.35 gives close to optimal labeling. Variation in the Sn/DTTA ratio by a factor of two negatively impacts upon both labeling efficiency in vitro and circulation half-life in vivo. Potential uses for technetium-labeled lipid vesicles with extended circulation half-life are discussed.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/1,2-dipalmitoyl-3-phosphatidylethano...,
http://linkedlifedata.com/resource/pubmed/chemical/Chelating Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Organotechnetium Compounds,
http://linkedlifedata.com/resource/pubmed/chemical/Pentetic Acid,
http://linkedlifedata.com/resource/pubmed/chemical/Phosphatidylethanolamines,
http://linkedlifedata.com/resource/pubmed/chemical/Polymers,
http://linkedlifedata.com/resource/pubmed/chemical/Tin,
http://linkedlifedata.com/resource/pubmed/chemical/diethylenetriaminetetraacetic acid
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pubmed:status |
MEDLINE
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pubmed:month |
Jan
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pubmed:issn |
0969-8051
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
21
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
89-96
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:9234269-Animals,
pubmed-meshheading:9234269-Chelating Agents,
pubmed-meshheading:9234269-Isotope Labeling,
pubmed-meshheading:9234269-Organotechnetium Compounds,
pubmed-meshheading:9234269-Oxidation-Reduction,
pubmed-meshheading:9234269-Pentetic Acid,
pubmed-meshheading:9234269-Phosphatidylethanolamines,
pubmed-meshheading:9234269-Polymers,
pubmed-meshheading:9234269-Rabbits,
pubmed-meshheading:9234269-Tin,
pubmed-meshheading:9234269-Tissue Distribution
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pubmed:year |
1994
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pubmed:articleTitle |
99mTc-labeling of lipid vesicles containing the lipophilic chelator PE-DTTA: effect of tin-to-chelate ratio, chelate content and surface polymer on labeling efficiency and biodistribution behavior.
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pubmed:affiliation |
Department of Radiology, University of British Columbia, Vancouver, Canada.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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