Optimized MRI contrast for on-resonance proton exchange processes of PARACEST agents in biological systems.
Identifieur interne : 000329 ( Ncbi/Merge ); précédent : 000328; suivant : 000330Optimized MRI contrast for on-resonance proton exchange processes of PARACEST agents in biological systems.
Auteurs : Alex X. Li [Canada] ; Mojmir Suchy ; Craig K. Jones ; Robert H E. Hudson ; Ravi S. Menon ; Robert BarthaSource :
- Magnetic resonance in medicine [ 1522-2594 ] ; 2009.
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Abstract
Image contrast associated with paramagnetic chemical exchange saturation transfer agents can be generated by off-resonance irradiation of agent-bound water or amide protons or on-resonance irradiation of bulk water. Previously, a four-pool model was developed to describe an in vivo system. The model incorporated the magnetization transfer effect from macromolecules when using off-resonance irradiation. In the current study, this four-pool model is modified to describe the in vivo system when using on-resonance irradiation. The influences of pulse power, pulse duration, the chemical shift of bound water, the proton exchange rate between bulk water and bound water, and agent concentration on the on-resonance paramagnetic agent chemical exchange effects were simulated using a WALTZ-16 pulse train in the absence and presence of the macromolecule pool. The results demonstrated that while contrast increases with pulse duration in aqueous solution, there is an optimal pulse duration that maximizes on-resonance paramagnetic agent chemical exchange effects contrast in vivo. This predication was verified by experimental spectroscopic and imaging results from aqueous solution, bovine serum albumin phantoms, and a tissue phantom containing thulium-DOTAM (1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetamide)-glycine-lysine. This model can be used to optimize sequence parameters to maximize in vivo on-resonance paramagnetic agent chemical exchange effects contrast.
DOI: 10.1002/mrm.22134
PubMed: 19780147
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Jones</name></author><author><name sortKey="Hudson, Robert H E" sort="Hudson, Robert H E" uniqKey="Hudson R" first="Robert H E" last="Hudson">Robert H E. Hudson</name></author><author><name sortKey="Menon, Ravi S" sort="Menon, Ravi S" uniqKey="Menon R" first="Ravi S" last="Menon">Ravi S. Menon</name></author><author><name sortKey="Bartha, Robert" sort="Bartha, Robert" uniqKey="Bartha R" first="Robert" last="Bartha">Robert Bartha</name></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="2009">2009</date><idno type="doi">10.1002/mrm.22134</idno><idno type="RBID">pubmed:19780147</idno><idno type="pmid">19780147</idno><idno type="wicri:Area/PubMed/Corpus">000516</idno><idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Corpus" wicri:corpus="PubMed">000516</idno><idno type="wicri:Area/PubMed/Curation">000516</idno><idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Curation">000516</idno><idno type="wicri:Area/PubMed/Checkpoint">000516</idno><idno type="wicri:explorRef" wicri:stream="Checkpoint" wicri:step="PubMed">000516</idno><idno type="wicri:Area/Ncbi/Merge">000329</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en">Optimized MRI contrast for on-resonance proton exchange processes of PARACEST agents in biological systems.</title><author><name sortKey="Li, Alex X" sort="Li, Alex X" uniqKey="Li A" first="Alex X" last="Li">Alex X. Li</name><affiliation wicri:level="1"><nlm:affiliation>Center for Functional and Metabolic Mapping, Robarts Research Institute, London, Ontario, Canada.</nlm:affiliation><country xml:lang="fr">Canada</country><wicri:regionArea>Center for Functional and Metabolic Mapping, Robarts Research Institute, London, Ontario</wicri:regionArea><wicri:noRegion>Ontario</wicri:noRegion></affiliation></author><author><name sortKey="Suchy, Mojmir" sort="Suchy, Mojmir" uniqKey="Suchy M" first="Mojmir" last="Suchy">Mojmir Suchy</name></author><author><name sortKey="Jones, Craig K" sort="Jones, Craig K" uniqKey="Jones C" first="Craig K" last="Jones">Craig K. Jones</name></author><author><name sortKey="Hudson, Robert H E" sort="Hudson, Robert H E" uniqKey="Hudson R" first="Robert H E" last="Hudson">Robert H E. Hudson</name></author><author><name sortKey="Menon, Ravi S" sort="Menon, Ravi S" uniqKey="Menon R" first="Ravi S" last="Menon">Ravi S. Menon</name></author><author><name sortKey="Bartha, Robert" sort="Bartha, Robert" uniqKey="Bartha R" first="Robert" last="Bartha">Robert Bartha</name></author></analytic><series><title level="j">Magnetic resonance in medicine</title><idno type="eISSN">1522-2594</idno><imprint><date when="2009" type="published">2009</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Algorithms</term><term>Computer Simulation</term><term>Contrast Media</term><term>Image Enhancement (methods)</term><term>Image Interpretation, Computer-Assisted (methods)</term><term>Magnetic Resonance Imaging (methods)</term><term>Models, Biological</term><term>Protons</term><term>Reproducibility of Results</term><term>Sensitivity and Specificity</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Algorithmes</term><term>Amélioration d'image ()</term><term>Imagerie par résonance magnétique ()</term><term>Interprétation d'image assistée par ordinateur ()</term><term>Modèles biologiques</term><term>Produits de contraste</term><term>Protons</term><term>Reproductibilité des résultats</term><term>Sensibilité et spécificité</term><term>Simulation numérique</term></keywords><keywords scheme="MESH" type="chemical" xml:lang="en"><term>Contrast Media</term><term>Protons</term></keywords><keywords scheme="MESH" qualifier="methods" xml:lang="en"><term>Image Enhancement</term><term>Image Interpretation, Computer-Assisted</term><term>Magnetic Resonance Imaging</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Algorithms</term><term>Computer Simulation</term><term>Models, Biological</term><term>Reproducibility of Results</term><term>Sensitivity and Specificity</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Algorithmes</term><term>Amélioration d'image</term><term>Imagerie par résonance magnétique</term><term>Interprétation d'image assistée par ordinateur</term><term>Modèles biologiques</term><term>Produits de contraste</term><term>Protons</term><term>Reproductibilité des résultats</term><term>Sensibilité et spécificité</term><term>Simulation numérique</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Image contrast associated with paramagnetic chemical exchange saturation transfer agents can be generated by off-resonance irradiation of agent-bound water or amide protons or on-resonance irradiation of bulk water. Previously, a four-pool model was developed to describe an in vivo system. The model incorporated the magnetization transfer effect from macromolecules when using off-resonance irradiation. In the current study, this four-pool model is modified to describe the in vivo system when using on-resonance irradiation. The influences of pulse power, pulse duration, the chemical shift of bound water, the proton exchange rate between bulk water and bound water, and agent concentration on the on-resonance paramagnetic agent chemical exchange effects were simulated using a WALTZ-16 pulse train in the absence and presence of the macromolecule pool. The results demonstrated that while contrast increases with pulse duration in aqueous solution, there is an optimal pulse duration that maximizes on-resonance paramagnetic agent chemical exchange effects contrast in vivo. This predication was verified by experimental spectroscopic and imaging results from aqueous solution, bovine serum albumin phantoms, and a tissue phantom containing thulium-DOTAM (1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetamide)-glycine-lysine. This model can be used to optimize sequence parameters to maximize in vivo on-resonance paramagnetic agent chemical exchange effects contrast.</div></front></TEI><pubmed><MedlineCitation Owner="NLM" Status="MEDLINE"><PMID Version="1">19780147</PMID><DateCreated><Year>2009</Year><Month>11</Month><Day>03</Day></DateCreated><DateCompleted><Year>2010</Year><Month>01</Month><Day>13</Day></DateCompleted><DateRevised><Year>2015</Year><Month>05</Month><Day>25</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Electronic">1522-2594</ISSN><JournalIssue CitedMedium="Internet"><Volume>62</Volume><Issue>5</Issue><PubDate><Year>2009</Year><Month>Nov</Month></PubDate></JournalIssue><Title>Magnetic resonance in medicine</Title><ISOAbbreviation>Magn Reson Med</ISOAbbreviation></Journal><ArticleTitle>Optimized MRI contrast for on-resonance proton exchange processes of PARACEST agents in biological systems.</ArticleTitle><Pagination><MedlinePgn>1282-91</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1002/mrm.22134</ELocationID><Abstract><AbstractText>Image contrast associated with paramagnetic chemical exchange saturation transfer agents can be generated by off-resonance irradiation of agent-bound water or amide protons or on-resonance irradiation of bulk water. Previously, a four-pool model was developed to describe an in vivo system. The model incorporated the magnetization transfer effect from macromolecules when using off-resonance irradiation. In the current study, this four-pool model is modified to describe the in vivo system when using on-resonance irradiation. The influences of pulse power, pulse duration, the chemical shift of bound water, the proton exchange rate between bulk water and bound water, and agent concentration on the on-resonance paramagnetic agent chemical exchange effects were simulated using a WALTZ-16 pulse train in the absence and presence of the macromolecule pool. The results demonstrated that while contrast increases with pulse duration in aqueous solution, there is an optimal pulse duration that maximizes on-resonance paramagnetic agent chemical exchange effects contrast in vivo. This predication was verified by experimental spectroscopic and imaging results from aqueous solution, bovine serum albumin phantoms, and a tissue phantom containing thulium-DOTAM (1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetamide)-glycine-lysine. 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Hudson</name><name sortKey="Jones, Craig K" sort="Jones, Craig K" uniqKey="Jones C" first="Craig K" last="Jones">Craig K. Jones</name><name sortKey="Menon, Ravi S" sort="Menon, Ravi S" uniqKey="Menon R" first="Ravi S" last="Menon">Ravi S. Menon</name><name sortKey="Suchy, Mojmir" sort="Suchy, Mojmir" uniqKey="Suchy M" first="Mojmir" last="Suchy">Mojmir Suchy</name></noCountry><country name="Canada"><noRegion><name sortKey="Li, Alex X" sort="Li, Alex X" uniqKey="Li A" first="Alex X" last="Li">Alex X. Li</name></noRegion></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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