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Synthesis and Biocompatibility Studies of New Iminodiacetic Acid Derivatives

Background: Iminodiacetic acid (IDA) derivatives can be used as ligands to form complexes with technetium, with potential application as hepatobiliary diagnostic agents. The aim of this study was to synthesize five novel IDA derivatives and to compare their effects on plasma haemostasis with clinica...

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Autores principales: Markowicz-Piasecka, Magdalena, Dębski, Piotr, Mikiciuk-Olasik, Elżbieta, Sikora, Joanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149924/
https://www.ncbi.nlm.nih.gov/pubmed/29258275
http://dx.doi.org/10.3390/molecules22122265
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author Markowicz-Piasecka, Magdalena
Dębski, Piotr
Mikiciuk-Olasik, Elżbieta
Sikora, Joanna
author_facet Markowicz-Piasecka, Magdalena
Dębski, Piotr
Mikiciuk-Olasik, Elżbieta
Sikora, Joanna
author_sort Markowicz-Piasecka, Magdalena
collection PubMed
description Background: Iminodiacetic acid (IDA) derivatives can be used as ligands to form complexes with technetium, with potential application as hepatobiliary diagnostic agents. The aim of this study was to synthesize five novel IDA derivatives and to compare their effects on plasma haemostasis with clinically approved ligands for technetium complexation. Methods: The influence of synthesized IDA derivatives on plasma haemostasis was evaluated spectrophotometrically by clot formation and lysis test (CL-test), coagulation assay, Prothrombin Time and Activated Partial Tromboplastin Time. The effects of the tested compounds on erythrocytes were assessed using haemolysis assays, microscopy and flow cytometry studies. Results: Despite their significant influence on the kinetic parameters of the process of clot formation and fibrinolysis, the tested ligands, at potential diagnostic concentrations, did not alter the overall potential of clot formation and lysis (CL(AUC)). At potential diagnostic concentrations (0.4 μmol/mL) all the tested compounds showed no adverse effects on the membranes of RBCs (Red Blood Cells). Conclusion: IDA derivatives with methoxy substituents in aromatic ring, exert multidirectional effects on plasma haemostasis and should be considered safe as their significant impacts were mostly observed at 4 μmol/mL, which is about 10-fold higher than the theoretical plasma concentrations of these compounds.
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spelling pubmed-61499242018-11-13 Synthesis and Biocompatibility Studies of New Iminodiacetic Acid Derivatives Markowicz-Piasecka, Magdalena Dębski, Piotr Mikiciuk-Olasik, Elżbieta Sikora, Joanna Molecules Article Background: Iminodiacetic acid (IDA) derivatives can be used as ligands to form complexes with technetium, with potential application as hepatobiliary diagnostic agents. The aim of this study was to synthesize five novel IDA derivatives and to compare their effects on plasma haemostasis with clinically approved ligands for technetium complexation. Methods: The influence of synthesized IDA derivatives on plasma haemostasis was evaluated spectrophotometrically by clot formation and lysis test (CL-test), coagulation assay, Prothrombin Time and Activated Partial Tromboplastin Time. The effects of the tested compounds on erythrocytes were assessed using haemolysis assays, microscopy and flow cytometry studies. Results: Despite their significant influence on the kinetic parameters of the process of clot formation and fibrinolysis, the tested ligands, at potential diagnostic concentrations, did not alter the overall potential of clot formation and lysis (CL(AUC)). At potential diagnostic concentrations (0.4 μmol/mL) all the tested compounds showed no adverse effects on the membranes of RBCs (Red Blood Cells). Conclusion: IDA derivatives with methoxy substituents in aromatic ring, exert multidirectional effects on plasma haemostasis and should be considered safe as their significant impacts were mostly observed at 4 μmol/mL, which is about 10-fold higher than the theoretical plasma concentrations of these compounds. MDPI 2017-12-18 /pmc/articles/PMC6149924/ /pubmed/29258275 http://dx.doi.org/10.3390/molecules22122265 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Markowicz-Piasecka, Magdalena
Dębski, Piotr
Mikiciuk-Olasik, Elżbieta
Sikora, Joanna
Synthesis and Biocompatibility Studies of New Iminodiacetic Acid Derivatives
title Synthesis and Biocompatibility Studies of New Iminodiacetic Acid Derivatives
title_full Synthesis and Biocompatibility Studies of New Iminodiacetic Acid Derivatives
title_fullStr Synthesis and Biocompatibility Studies of New Iminodiacetic Acid Derivatives
title_full_unstemmed Synthesis and Biocompatibility Studies of New Iminodiacetic Acid Derivatives
title_short Synthesis and Biocompatibility Studies of New Iminodiacetic Acid Derivatives
title_sort synthesis and biocompatibility studies of new iminodiacetic acid derivatives
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149924/
https://www.ncbi.nlm.nih.gov/pubmed/29258275
http://dx.doi.org/10.3390/molecules22122265
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