Platas-Iglesias, Carlos

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orcid::0000-0002-6989-9654
  • Platas-Iglesias, Carlos (2)
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Supplementary data for the article: Cakić, N.; Verbić, T. Ž.; Jelić, R. M.; Platas-Iglesias, C.; Angelovski, G. Synthesis and Characterisation of Bismacrocyclic DO3A-Amide Derivatives - An Approach towards Metal-Responsive PARACEST Agents. Dalton Transactions 2016, 45 (15), 6555–6565. https://doi.org/10.1039/c5dt04625d

Cakić, Nevenka; Verbić, Tatjana; Jelić, Ratomir; Platas-Iglesias, Carlos; Angelovski, Goran

(Royal Soc Chemistry, Cambridge, 2016)

TY  - DATA
AU  - Cakić, Nevenka
AU  - Verbić, Tatjana
AU  - Jelić, Ratomir
AU  - Platas-Iglesias, Carlos
AU  - Angelovski, Goran
PY  - 2016
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/3623
PB  - Royal Soc Chemistry, Cambridge
T2  - Dalton Transactions
T1  - Supplementary data for the article: Cakić, N.; Verbić, T. Ž.; Jelić, R. M.; Platas-Iglesias, C.; Angelovski, G. Synthesis and Characterisation of Bismacrocyclic DO3A-Amide Derivatives - An Approach towards Metal-Responsive PARACEST Agents. Dalton Transactions 2016, 45 (15), 6555–6565. https://doi.org/10.1039/c5dt04625d
UR  - https://hdl.handle.net/21.15107/rcub_cherry_3623
ER  - 
@misc{
author = "Cakić, Nevenka and Verbić, Tatjana and Jelić, Ratomir and Platas-Iglesias, Carlos and Angelovski, Goran",
year = "2016",
publisher = "Royal Soc Chemistry, Cambridge",
journal = "Dalton Transactions",
title = "Supplementary data for the article: Cakić, N.; Verbić, T. Ž.; Jelić, R. M.; Platas-Iglesias, C.; Angelovski, G. Synthesis and Characterisation of Bismacrocyclic DO3A-Amide Derivatives - An Approach towards Metal-Responsive PARACEST Agents. Dalton Transactions 2016, 45 (15), 6555–6565. https://doi.org/10.1039/c5dt04625d",
url = "https://hdl.handle.net/21.15107/rcub_cherry_3623"
}
Cakić, N., Verbić, T., Jelić, R., Platas-Iglesias, C.,& Angelovski, G.. (2016). Supplementary data for the article: Cakić, N.; Verbić, T. Ž.; Jelić, R. M.; Platas-Iglesias, C.; Angelovski, G. Synthesis and Characterisation of Bismacrocyclic DO3A-Amide Derivatives - An Approach towards Metal-Responsive PARACEST Agents. Dalton Transactions 2016, 45 (15), 6555–6565. https://doi.org/10.1039/c5dt04625d. in Dalton Transactions
Royal Soc Chemistry, Cambridge..
https://hdl.handle.net/21.15107/rcub_cherry_3623
Cakić N, Verbić T, Jelić R, Platas-Iglesias C, Angelovski G. Supplementary data for the article: Cakić, N.; Verbić, T. Ž.; Jelić, R. M.; Platas-Iglesias, C.; Angelovski, G. Synthesis and Characterisation of Bismacrocyclic DO3A-Amide Derivatives - An Approach towards Metal-Responsive PARACEST Agents. Dalton Transactions 2016, 45 (15), 6555–6565. https://doi.org/10.1039/c5dt04625d. in Dalton Transactions. 2016;.
https://hdl.handle.net/21.15107/rcub_cherry_3623 .
Cakić, Nevenka, Verbić, Tatjana, Jelić, Ratomir, Platas-Iglesias, Carlos, Angelovski, Goran, "Supplementary data for the article: Cakić, N.; Verbić, T. Ž.; Jelić, R. M.; Platas-Iglesias, C.; Angelovski, G. Synthesis and Characterisation of Bismacrocyclic DO3A-Amide Derivatives - An Approach towards Metal-Responsive PARACEST Agents. Dalton Transactions 2016, 45 (15), 6555–6565. https://doi.org/10.1039/c5dt04625d" in Dalton Transactions (2016),
https://hdl.handle.net/21.15107/rcub_cherry_3623 .

Synthesis and characterisation of bismacrocyclic DO3A-amide derivatives - an approach towards metal-responsive PARACEST agents

Cakić, Nevenka; Verbić, Tatjana; Jelić, Ratomir; Platas-Iglesias, Carlos; Angelovski, Goran

(Royal Soc Chemistry, Cambridge, 2016)

TY  - JOUR
AU  - Cakić, Nevenka
AU  - Verbić, Tatjana
AU  - Jelić, Ratomir
AU  - Platas-Iglesias, Carlos
AU  - Angelovski, Goran
PY  - 2016
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1911
AB  - Three new bismacrocyclic Ln(3+) chelates consisting of triamide derivatives of cyclen with glycine, methyl and tert-butyl substituents (L1-3, respectively) linked to an acyclic EGTA-derived calcium chelator were synthesised as potential MRI contrast agents (EGTA -ethylene glycol-bis(2-aminoethylether)-N, N, N', N'-tetraacetic acid). Eu3+ and Yb3+ complexes of L1-3 were investigated as chemical exchange saturation transfer (CEST) agents. Moderate to minor CEST effects were observed for Eu2L1, Eu2L2 and Yb2L2 complexes in the absence of Ca2+, with negligible changes upon addition of this metal ion. Luminescence steady-state emission and lifetime experiments did not reveal any changes in the coordination environment of the complexes, while the number of inner-sphere water molecules remained constant in the absence and presence of Ca2+. The protonation constants of Eu2L1 and Eu2L2 and stability constants of their complexes with Ca2+, Mg2+ and Zn2+ were determined by means of potentiometric titrations. The results show that the charge of the complex dramatically affects the protonation constants of the EGTA-binding unit. The stability constants of the complexes formed with Ca2+, Mg2+ and Zn2+ are several orders of magnitude lower than those of EGTA. These findings indicate that the nature of Ln(3+) chelates and their charge are the main reasons for the observed results and weaker response of these EGTA-derived triamide derivatives compared to their tricarboxylate analogues.
PB  - Royal Soc Chemistry, Cambridge
T2  - Dalton Transactions
T1  - Synthesis and characterisation of bismacrocyclic DO3A-amide derivatives - an approach towards metal-responsive PARACEST agents
VL  - 45
IS  - 15
SP  - 6555
EP  - 6565
DO  - 10.1039/c5dt04625d
ER  - 
@article{
author = "Cakić, Nevenka and Verbić, Tatjana and Jelić, Ratomir and Platas-Iglesias, Carlos and Angelovski, Goran",
year = "2016",
abstract = "Three new bismacrocyclic Ln(3+) chelates consisting of triamide derivatives of cyclen with glycine, methyl and tert-butyl substituents (L1-3, respectively) linked to an acyclic EGTA-derived calcium chelator were synthesised as potential MRI contrast agents (EGTA -ethylene glycol-bis(2-aminoethylether)-N, N, N', N'-tetraacetic acid). Eu3+ and Yb3+ complexes of L1-3 were investigated as chemical exchange saturation transfer (CEST) agents. Moderate to minor CEST effects were observed for Eu2L1, Eu2L2 and Yb2L2 complexes in the absence of Ca2+, with negligible changes upon addition of this metal ion. Luminescence steady-state emission and lifetime experiments did not reveal any changes in the coordination environment of the complexes, while the number of inner-sphere water molecules remained constant in the absence and presence of Ca2+. The protonation constants of Eu2L1 and Eu2L2 and stability constants of their complexes with Ca2+, Mg2+ and Zn2+ were determined by means of potentiometric titrations. The results show that the charge of the complex dramatically affects the protonation constants of the EGTA-binding unit. The stability constants of the complexes formed with Ca2+, Mg2+ and Zn2+ are several orders of magnitude lower than those of EGTA. These findings indicate that the nature of Ln(3+) chelates and their charge are the main reasons for the observed results and weaker response of these EGTA-derived triamide derivatives compared to their tricarboxylate analogues.",
publisher = "Royal Soc Chemistry, Cambridge",
journal = "Dalton Transactions",
title = "Synthesis and characterisation of bismacrocyclic DO3A-amide derivatives - an approach towards metal-responsive PARACEST agents",
volume = "45",
number = "15",
pages = "6555-6565",
doi = "10.1039/c5dt04625d"
}
Cakić, N., Verbić, T., Jelić, R., Platas-Iglesias, C.,& Angelovski, G.. (2016). Synthesis and characterisation of bismacrocyclic DO3A-amide derivatives - an approach towards metal-responsive PARACEST agents. in Dalton Transactions
Royal Soc Chemistry, Cambridge., 45(15), 6555-6565.
https://doi.org/10.1039/c5dt04625d
Cakić N, Verbić T, Jelić R, Platas-Iglesias C, Angelovski G. Synthesis and characterisation of bismacrocyclic DO3A-amide derivatives - an approach towards metal-responsive PARACEST agents. in Dalton Transactions. 2016;45(15):6555-6565.
doi:10.1039/c5dt04625d .
Cakić, Nevenka, Verbić, Tatjana, Jelić, Ratomir, Platas-Iglesias, Carlos, Angelovski, Goran, "Synthesis and characterisation of bismacrocyclic DO3A-amide derivatives - an approach towards metal-responsive PARACEST agents" in Dalton Transactions, 45, no. 15 (2016):6555-6565,
https://doi.org/10.1039/c5dt04625d . .
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