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Hydrothermal Synthesize of HF-Free MIL-100(Fe) for Isoniazid-Drug Delivery

Sustainable development of drug delivery materials with good biocompatibility and controlled-release is a popular topic among researchers. In this research study, we demonstrated the potential of the metal-organic framework, that is MIL-100(Fe), as a drug delivery platform for isoniazid (INH). The M...

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Autores principales: Simon, Meta A., Anggraeni, Erlina, Soetaredjo, Felycia Edi, Santoso, Shella Permasari, Irawaty, Wenny, Thanh, Truong Chi, Hartono, Sandy Budi, Yuliana, Maria, Ismadji, Suryadi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6858337/
https://www.ncbi.nlm.nih.gov/pubmed/31729434
http://dx.doi.org/10.1038/s41598-019-53436-3
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author Simon, Meta A.
Anggraeni, Erlina
Soetaredjo, Felycia Edi
Santoso, Shella Permasari
Irawaty, Wenny
Thanh, Truong Chi
Hartono, Sandy Budi
Yuliana, Maria
Ismadji, Suryadi
author_facet Simon, Meta A.
Anggraeni, Erlina
Soetaredjo, Felycia Edi
Santoso, Shella Permasari
Irawaty, Wenny
Thanh, Truong Chi
Hartono, Sandy Budi
Yuliana, Maria
Ismadji, Suryadi
author_sort Simon, Meta A.
collection PubMed
description Sustainable development of drug delivery materials with good biocompatibility and controlled-release is a popular topic among researchers. In this research study, we demonstrated the potential of the metal-organic framework, that is MIL-100(Fe), as a drug delivery platform for isoniazid (INH). The MIL-100(Fe) was prepared by using the hydrofluoric acid-free hydrothermal method. Several physical measurements were conducted to characterize the MIL-100(Fe), including x-ray diffraction (XRD), scanning electron microscopy (SEM), nitrogen sorption, and thermal-gravimetric (TG). The synthesized MIL-100(Fe) has octahedron-shaped particles with superior properties, that is large surface area (1456.10 m(2)/g) and pore volume (1.25 cm(3)/g). The drug loading rate and capacity were determined by means of adsorption kinetic and isotherm. The studied INH@MIL-100(Fe) adsorption system kinetics follow the pseudo-first-order model, while the isotherm system follows the Langmuir model with the maximum adsorption capacity of 128.5 mg/g at 30 °C. MIL-100(Fe) shows adequate biocompatibility, also exhibits a reasonable and controlled drug release kinetics. The results obtained show that MIL-100 (Fe) can be a good choice of drug delivery platform among other available platforms.
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spelling pubmed-68583372019-11-27 Hydrothermal Synthesize of HF-Free MIL-100(Fe) for Isoniazid-Drug Delivery Simon, Meta A. Anggraeni, Erlina Soetaredjo, Felycia Edi Santoso, Shella Permasari Irawaty, Wenny Thanh, Truong Chi Hartono, Sandy Budi Yuliana, Maria Ismadji, Suryadi Sci Rep Article Sustainable development of drug delivery materials with good biocompatibility and controlled-release is a popular topic among researchers. In this research study, we demonstrated the potential of the metal-organic framework, that is MIL-100(Fe), as a drug delivery platform for isoniazid (INH). The MIL-100(Fe) was prepared by using the hydrofluoric acid-free hydrothermal method. Several physical measurements were conducted to characterize the MIL-100(Fe), including x-ray diffraction (XRD), scanning electron microscopy (SEM), nitrogen sorption, and thermal-gravimetric (TG). The synthesized MIL-100(Fe) has octahedron-shaped particles with superior properties, that is large surface area (1456.10 m(2)/g) and pore volume (1.25 cm(3)/g). The drug loading rate and capacity were determined by means of adsorption kinetic and isotherm. The studied INH@MIL-100(Fe) adsorption system kinetics follow the pseudo-first-order model, while the isotherm system follows the Langmuir model with the maximum adsorption capacity of 128.5 mg/g at 30 °C. MIL-100(Fe) shows adequate biocompatibility, also exhibits a reasonable and controlled drug release kinetics. The results obtained show that MIL-100 (Fe) can be a good choice of drug delivery platform among other available platforms. Nature Publishing Group UK 2019-11-15 /pmc/articles/PMC6858337/ /pubmed/31729434 http://dx.doi.org/10.1038/s41598-019-53436-3 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Simon, Meta A.
Anggraeni, Erlina
Soetaredjo, Felycia Edi
Santoso, Shella Permasari
Irawaty, Wenny
Thanh, Truong Chi
Hartono, Sandy Budi
Yuliana, Maria
Ismadji, Suryadi
Hydrothermal Synthesize of HF-Free MIL-100(Fe) for Isoniazid-Drug Delivery
title Hydrothermal Synthesize of HF-Free MIL-100(Fe) for Isoniazid-Drug Delivery
title_full Hydrothermal Synthesize of HF-Free MIL-100(Fe) for Isoniazid-Drug Delivery
title_fullStr Hydrothermal Synthesize of HF-Free MIL-100(Fe) for Isoniazid-Drug Delivery
title_full_unstemmed Hydrothermal Synthesize of HF-Free MIL-100(Fe) for Isoniazid-Drug Delivery
title_short Hydrothermal Synthesize of HF-Free MIL-100(Fe) for Isoniazid-Drug Delivery
title_sort hydrothermal synthesize of hf-free mil-100(fe) for isoniazid-drug delivery
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6858337/
https://www.ncbi.nlm.nih.gov/pubmed/31729434
http://dx.doi.org/10.1038/s41598-019-53436-3
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