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001-es BibID:BIBFORM112577
035-os BibID:(WoS)000431833500088 (Scopus)85046700183
Első szerző:Aime, Silvio
Cím:Exploiting the Proton Exchange as an Additional Route to Enhance the Relaxivity of Paramagnetic MRI Contrast Agents / Silvio Aime, Simona Baroni, Daniela Delli Castelli, Ernő Brücher, Istvan Fábián, Sonia Colombo Serra, Alberto Fringuello Mingo, Roberta Napolitano, Luciano Lattuada, Fabio Tedoldi, Zsolt Baranyai
Dátum:2018
ISSN:0020-1669 1520-510X
Megjegyzések:The relaxivity of Gd(HP-DO3A) was studied as a function of pH and buffer composition in order to identify the main factors of the observed relaxation enhancement due to the exchange of the coordinated hydroxyl proton. It was established that the paramagnetic relaxation time, T1M, of the coordinated hydroxyl proton is about 50% shorter than that of the protons in the coordinated water molecule. The control of the pK of the coordinated alcoholic ?OH moiety in the ligand is fundamental to utilize the proton exchange enhanced relaxivity under physio/pathologic conditions. A new derivative of Gd(HP-DO3A) was synthesized by replacing the ?CH3 group with a ?CF3 moiety. In this complex, the ?OH group becomes more acidic. Consequently, the maximum contribution of the proton exchange to the relaxivity is shifted to a lower pH region with the fluorinated ligand.
Tárgyszavak:Természettudományok Kémiai tudományok idegen nyelvű folyóiratközlemény külföldi lapban
folyóiratcikk
relaxivity
MRI
proton exchange
Megjelenés:Inorganic Chemistry. - 57 : 9 (2018), p. 5567-5574. -
További szerzők:Baroni, Simona Castelli, Daniela Delli Brücher Ernő (1935-) (vegyész) Fábián István (1956-) (vegyész) Serra, Sonia Colombo Fringuello Mingo, Alberto Napolitano, Roberta Lattuada, Luciano Tedoldi, Fabio Baranyai Zsolt
Pályázati támogatás:124983
OTKA
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001-es BibID:BIBFORM103334
035-os BibID:(WOS)000555801800006 (Scopus)85089285156
Első szerző:Leone, Loredana
Cím:Acid-catalyzed proton exchange as a novel approach for relaxivity enhancement in Gd-HPDO3A-like complexes / Loredana Leone, Mariangela Boccalon, Giuseppe Ferrauto, István Fábián, Zsolt Baranyai, Lorenzo Tei
Dátum:2020
ISSN:2041-6520 2041-6539
Megjegyzések:A current challenge in medical diagnostics is how to obtain high MRI relaxation enhancement using Gd-III-based contrast agents (CAs) containing the minimum concentration of Gd(III)ions. We report that in GdHPDO3A-like complexes a primary amide group located in close proximity to the coordinated hydroxyl group can provide a strong relaxivity enhancement at slightly acidic pH. A maximum relaxivity ofr(1)= 9.8 mM(-1)s(-1)(20 MHz, 298 K) at acidic pH was achieved, which is more than double that of clinically approved MRI contrast agents under identical conditions. This effect was found to strongly depend on the number of amide protons,i.e.it decreases with a secondary amide group and almost completely vanishes with a tertiary amide. This relaxivity enhancement is attributed to an acid-catalyzed proton exchange process between the metal-coordinated OH group, the amide protons and second sphere water molecules. The mechanism and kinetics of the corresponding H(+)assisted exchange process are discussed in detail and a novel simultaneous double-site proton exchange mechanism is proposed. Furthermore,H-1 and(17)O NMR relaxometry, Chemical Exchange Saturation Transfer (CEST) on the corresponding Eu(III)complexes, and thermodynamic and kinetic studies are reported. These highlight the optimal physico-chemical properties required to achieve high relaxivity with this series of Gd-III-complexes. Thus, proton exchange provides an important opportunity to enhance the relaxivity of contrast agents, providing that labile protons close to the paramagnetic center can contribute.
Tárgyszavak:Természettudományok Kémiai tudományok idegen nyelvű folyóiratközlemény külföldi lapban
folyóiratcikk
Megjelenés:Chemical Science. - 11 : 30 (2020), p. 7829-7835. -
További szerzők:Boccalon, Mariangela Ferrauto, Giuseppe Fábián István (1956-) (vegyész) Baranyai Zsolt Tei, Lorenzo
Pályázati támogatás:NKFIH-K-124983
Egyéb
Internet cím:Szerző által megadott URL
DOI
Intézményi repozitóriumban (DEA) tárolt változat
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