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Iron-Based Metal-Organic Frameworks as a Theranostic Carrier for Local Tuberculosis Therapy

PURPOSE: The purpose of the study was initial evaluation of applicability of metal organic framework (MOF) Fe-MIL-101-NH(2) as a theranostic carrier of antituberculous drug in terms of its functionality, i.e. drug loading, drug dissolution, magnetic resonance imaging (MRI) contrast and cytotoxic saf...

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Autores principales: Wyszogrodzka, Gabriela, Dorożyński, Przemysław, Gil, Barbara, Roth, Wieslaw J., Strzempek, Maciej, Marszałek, Bartosz, Węglarz, Władysław P., Menaszek, Elżbieta, Strzempek, Weronika, Kulinowski, Piotr
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5960001/
https://www.ncbi.nlm.nih.gov/pubmed/29777389
http://dx.doi.org/10.1007/s11095-018-2425-2
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author Wyszogrodzka, Gabriela
Dorożyński, Przemysław
Gil, Barbara
Roth, Wieslaw J.
Strzempek, Maciej
Marszałek, Bartosz
Węglarz, Władysław P.
Menaszek, Elżbieta
Strzempek, Weronika
Kulinowski, Piotr
author_facet Wyszogrodzka, Gabriela
Dorożyński, Przemysław
Gil, Barbara
Roth, Wieslaw J.
Strzempek, Maciej
Marszałek, Bartosz
Węglarz, Władysław P.
Menaszek, Elżbieta
Strzempek, Weronika
Kulinowski, Piotr
author_sort Wyszogrodzka, Gabriela
collection PubMed
description PURPOSE: The purpose of the study was initial evaluation of applicability of metal organic framework (MOF) Fe-MIL-101-NH(2) as a theranostic carrier of antituberculous drug in terms of its functionality, i.e. drug loading, drug dissolution, magnetic resonance imaging (MRI) contrast and cytotoxic safety. METHODS: Fe-MIL-101-NH(2) was characterized using X-ray powder diffraction, FTIR spectrometry and scanning electron microscopy. The particle size analysis was determined using laser diffraction. Magnetic resonance relaxometry and MRI were carried out on phantoms of the MOF system suspended in polymer solution. Drug dissolution studies were conducted using Franz cells. For MOF cytotoxicity, commercially available fibroblasts L929 were cultured in Eagle’s Minimum Essential Medium supplemented with 10% fetal bovine serum. RESULTS: MOF particles were loaded with 12% of isoniazid. The particle size (3.37–6.45 μm) depended on the micronization method used. The proposed drug delivery system can also serve as the MRI contrast agent. The drug dissolution showed extended release of isoniazid. MOF particles accumulated in the L929 fibroblast cytoplasmic area, suggesting MOF release the drug inside the cells. The cytotoxicity confirmed safety of MOF system. CONCLUSIONS: The application of MOF for extended release inhalable system proposes the novel strategy for delivery of standard antimycobacterial agents combined with monitoring of their distribution within the lung tissue.
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spelling pubmed-59600012018-05-24 Iron-Based Metal-Organic Frameworks as a Theranostic Carrier for Local Tuberculosis Therapy Wyszogrodzka, Gabriela Dorożyński, Przemysław Gil, Barbara Roth, Wieslaw J. Strzempek, Maciej Marszałek, Bartosz Węglarz, Władysław P. Menaszek, Elżbieta Strzempek, Weronika Kulinowski, Piotr Pharm Res Research Paper PURPOSE: The purpose of the study was initial evaluation of applicability of metal organic framework (MOF) Fe-MIL-101-NH(2) as a theranostic carrier of antituberculous drug in terms of its functionality, i.e. drug loading, drug dissolution, magnetic resonance imaging (MRI) contrast and cytotoxic safety. METHODS: Fe-MIL-101-NH(2) was characterized using X-ray powder diffraction, FTIR spectrometry and scanning electron microscopy. The particle size analysis was determined using laser diffraction. Magnetic resonance relaxometry and MRI were carried out on phantoms of the MOF system suspended in polymer solution. Drug dissolution studies were conducted using Franz cells. For MOF cytotoxicity, commercially available fibroblasts L929 were cultured in Eagle’s Minimum Essential Medium supplemented with 10% fetal bovine serum. RESULTS: MOF particles were loaded with 12% of isoniazid. The particle size (3.37–6.45 μm) depended on the micronization method used. The proposed drug delivery system can also serve as the MRI contrast agent. The drug dissolution showed extended release of isoniazid. MOF particles accumulated in the L929 fibroblast cytoplasmic area, suggesting MOF release the drug inside the cells. The cytotoxicity confirmed safety of MOF system. CONCLUSIONS: The application of MOF for extended release inhalable system proposes the novel strategy for delivery of standard antimycobacterial agents combined with monitoring of their distribution within the lung tissue. Springer US 2018-05-18 2018 /pmc/articles/PMC5960001/ /pubmed/29777389 http://dx.doi.org/10.1007/s11095-018-2425-2 Text en © The Author(s) 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Research Paper
Wyszogrodzka, Gabriela
Dorożyński, Przemysław
Gil, Barbara
Roth, Wieslaw J.
Strzempek, Maciej
Marszałek, Bartosz
Węglarz, Władysław P.
Menaszek, Elżbieta
Strzempek, Weronika
Kulinowski, Piotr
Iron-Based Metal-Organic Frameworks as a Theranostic Carrier for Local Tuberculosis Therapy
title Iron-Based Metal-Organic Frameworks as a Theranostic Carrier for Local Tuberculosis Therapy
title_full Iron-Based Metal-Organic Frameworks as a Theranostic Carrier for Local Tuberculosis Therapy
title_fullStr Iron-Based Metal-Organic Frameworks as a Theranostic Carrier for Local Tuberculosis Therapy
title_full_unstemmed Iron-Based Metal-Organic Frameworks as a Theranostic Carrier for Local Tuberculosis Therapy
title_short Iron-Based Metal-Organic Frameworks as a Theranostic Carrier for Local Tuberculosis Therapy
title_sort iron-based metal-organic frameworks as a theranostic carrier for local tuberculosis therapy
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5960001/
https://www.ncbi.nlm.nih.gov/pubmed/29777389
http://dx.doi.org/10.1007/s11095-018-2425-2
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