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Bactericidal and immunomodulatory properties of magnetic nanoparticles functionalized by 1,4-dihydropyridines

BACKGROUND: 1,4-Dihydropyridine (1,4-DHP) and its derivatives are well-known calcium channel blockers with antiarrhythmic and antihypertensive activities. These compounds exhibit pleiotropic effects including antimicrobial activities that rely on their positive charge and amphipathic nature. Use of...

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Autores principales: Niemirowicz-Laskowska, Katarzyna, Głuszek, Katarzyna, Piktel, Ewelina, Pajuste, Karlis, Durnaś, Bonita, Król, Grzegorz, Wilczewska, Agnieszka Z, Janmey, Paul A, Plotniece, Aiva, Bucki, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6001743/
https://www.ncbi.nlm.nih.gov/pubmed/29928120
http://dx.doi.org/10.2147/IJN.S157564
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author Niemirowicz-Laskowska, Katarzyna
Głuszek, Katarzyna
Piktel, Ewelina
Pajuste, Karlis
Durnaś, Bonita
Król, Grzegorz
Wilczewska, Agnieszka Z
Janmey, Paul A
Plotniece, Aiva
Bucki, Robert
author_facet Niemirowicz-Laskowska, Katarzyna
Głuszek, Katarzyna
Piktel, Ewelina
Pajuste, Karlis
Durnaś, Bonita
Król, Grzegorz
Wilczewska, Agnieszka Z
Janmey, Paul A
Plotniece, Aiva
Bucki, Robert
author_sort Niemirowicz-Laskowska, Katarzyna
collection PubMed
description BACKGROUND: 1,4-Dihydropyridine (1,4-DHP) and its derivatives are well-known calcium channel blockers with antiarrhythmic and antihypertensive activities. These compounds exhibit pleiotropic effects including antimicrobial activities that rely on their positive charge and amphipathic nature. Use of magnetic nanoparticles (MNPs) as carriers of 1,4-DHP modulates their properties and enables improved formulations with higher efficacy and less toxicity. METHODS: In this study, the antimicrobial and immunomodulatory activities of novel 1,4-DHP derivatives in free form and immobilized on MNPs were determined by evaluating pathogen outgrowth and proinflammatory cytokine release in experimental settings that involve incubation of various 1,4-DHPs with clinical isolates of bacteria or fungi as well as mammalian cell culture models. RESULTS: Conventional immobilization of 1,4-DHP on aminosilane-coated MNPs markedly enhances their antimicrobial activity compared to nonimmobilized molecules, in part because of the higher affinity of these nanosystems for bacterial cell wall components in the presence of human body fluids. CONCLUSION: Optimized nanosystems are characterized by improved biocompatibility and higher anti-inflammatory properties that provide new opportunities for the therapy of infectious diseases.
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spelling pubmed-60017432018-06-20 Bactericidal and immunomodulatory properties of magnetic nanoparticles functionalized by 1,4-dihydropyridines Niemirowicz-Laskowska, Katarzyna Głuszek, Katarzyna Piktel, Ewelina Pajuste, Karlis Durnaś, Bonita Król, Grzegorz Wilczewska, Agnieszka Z Janmey, Paul A Plotniece, Aiva Bucki, Robert Int J Nanomedicine Original Research BACKGROUND: 1,4-Dihydropyridine (1,4-DHP) and its derivatives are well-known calcium channel blockers with antiarrhythmic and antihypertensive activities. These compounds exhibit pleiotropic effects including antimicrobial activities that rely on their positive charge and amphipathic nature. Use of magnetic nanoparticles (MNPs) as carriers of 1,4-DHP modulates their properties and enables improved formulations with higher efficacy and less toxicity. METHODS: In this study, the antimicrobial and immunomodulatory activities of novel 1,4-DHP derivatives in free form and immobilized on MNPs were determined by evaluating pathogen outgrowth and proinflammatory cytokine release in experimental settings that involve incubation of various 1,4-DHPs with clinical isolates of bacteria or fungi as well as mammalian cell culture models. RESULTS: Conventional immobilization of 1,4-DHP on aminosilane-coated MNPs markedly enhances their antimicrobial activity compared to nonimmobilized molecules, in part because of the higher affinity of these nanosystems for bacterial cell wall components in the presence of human body fluids. CONCLUSION: Optimized nanosystems are characterized by improved biocompatibility and higher anti-inflammatory properties that provide new opportunities for the therapy of infectious diseases. Dove Medical Press 2018-06-11 /pmc/articles/PMC6001743/ /pubmed/29928120 http://dx.doi.org/10.2147/IJN.S157564 Text en © 2018 Niemirowicz-Laskowska et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Niemirowicz-Laskowska, Katarzyna
Głuszek, Katarzyna
Piktel, Ewelina
Pajuste, Karlis
Durnaś, Bonita
Król, Grzegorz
Wilczewska, Agnieszka Z
Janmey, Paul A
Plotniece, Aiva
Bucki, Robert
Bactericidal and immunomodulatory properties of magnetic nanoparticles functionalized by 1,4-dihydropyridines
title Bactericidal and immunomodulatory properties of magnetic nanoparticles functionalized by 1,4-dihydropyridines
title_full Bactericidal and immunomodulatory properties of magnetic nanoparticles functionalized by 1,4-dihydropyridines
title_fullStr Bactericidal and immunomodulatory properties of magnetic nanoparticles functionalized by 1,4-dihydropyridines
title_full_unstemmed Bactericidal and immunomodulatory properties of magnetic nanoparticles functionalized by 1,4-dihydropyridines
title_short Bactericidal and immunomodulatory properties of magnetic nanoparticles functionalized by 1,4-dihydropyridines
title_sort bactericidal and immunomodulatory properties of magnetic nanoparticles functionalized by 1,4-dihydropyridines
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6001743/
https://www.ncbi.nlm.nih.gov/pubmed/29928120
http://dx.doi.org/10.2147/IJN.S157564
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