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Multimetal organic frameworks as drug carriers: aceclofenac as a drug candidate
BACKGROUND: Multimetal organic frameworks (M-MOFs) were synthesized by including a second metal ion with the main base metal in the synthesis process to enhance their applications for drug delivery. Aceclofenac (ACF), a nonsteroidal anti-inflammatory analgesic drug of low aqueous solubility, was sel...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6305134/ https://www.ncbi.nlm.nih.gov/pubmed/30587925 http://dx.doi.org/10.2147/DDDT.S182983 |
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author | Al Haydar, Muder Abid, Hussein Rasool Sunderland, Bruce Wang, Shaobin |
author_facet | Al Haydar, Muder Abid, Hussein Rasool Sunderland, Bruce Wang, Shaobin |
author_sort | Al Haydar, Muder |
collection | PubMed |
description | BACKGROUND: Multimetal organic frameworks (M-MOFs) were synthesized by including a second metal ion with the main base metal in the synthesis process to enhance their applications for drug delivery. Aceclofenac (ACF), a nonsteroidal anti-inflammatory analgesic drug of low aqueous solubility, was selected as a candidate for the drug delivery system PURPOSE: This study aimed to evaluate the loading capacity (LC) and entrapment efficiency (EE) percentages of multi-Material of Institute Lavoisier (MIL)-100(Fe) (M-MIL-100(Fe)) for ACF. MATERIALS AND METHODS: Hydrothermal synthesis procedure was used to prepare multi-MIL-100(Fe) samples (Zn I-MIL-100(Fe), Zn II-MIL-100(Fe), Ca I-MIL-100(Fe), Ca II-MIL-100-(Fe), Mg I-MIL-100(Fe), Mg II-MIL-100(Fe), Mn I-MIL-100(Fe), and Mn II-MIL-100(Fe)). The characterization of M-MIL-100(Fe) samples was evaluated by X-ray powder diffraction (XRD), Fourier transform infrared spectra, scanning electron microscope (SEM), TGA, and N(2) adsorption isotherms. The LC of M-MIL-100(Fe) and EE of ACF were determined. Nuclear magnetic resonance (NMR) and zeta-potential analyses were employed to confirm qualitatively the drug loading within M-MIL-100(Fe). RESULTS: The ACF LC of MIL-100(Fe) was 27%, whereas the LC of M-MIL-100(Fe) was significantly increased and ranged from 37% in Ca I-MIL-100(Fe) to about 57% and 59% in Mn II-MIL-100(Fe) and Zn II-MIL-100(Fe), respectively. The ACF@M-MOFs release profiles showed slow release rates in phosphate buffer solutions at pH 6.8 and 7.4 as compared to the ACF@MIL-100(Fe). CONCLUSION: Therefore, M-MOFs showed a significant potential as a carrier for drug delivery systems. |
format | Online Article Text |
id | pubmed-6305134 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-63051342018-12-26 Multimetal organic frameworks as drug carriers: aceclofenac as a drug candidate Al Haydar, Muder Abid, Hussein Rasool Sunderland, Bruce Wang, Shaobin Drug Des Devel Ther Original Research BACKGROUND: Multimetal organic frameworks (M-MOFs) were synthesized by including a second metal ion with the main base metal in the synthesis process to enhance their applications for drug delivery. Aceclofenac (ACF), a nonsteroidal anti-inflammatory analgesic drug of low aqueous solubility, was selected as a candidate for the drug delivery system PURPOSE: This study aimed to evaluate the loading capacity (LC) and entrapment efficiency (EE) percentages of multi-Material of Institute Lavoisier (MIL)-100(Fe) (M-MIL-100(Fe)) for ACF. MATERIALS AND METHODS: Hydrothermal synthesis procedure was used to prepare multi-MIL-100(Fe) samples (Zn I-MIL-100(Fe), Zn II-MIL-100(Fe), Ca I-MIL-100(Fe), Ca II-MIL-100-(Fe), Mg I-MIL-100(Fe), Mg II-MIL-100(Fe), Mn I-MIL-100(Fe), and Mn II-MIL-100(Fe)). The characterization of M-MIL-100(Fe) samples was evaluated by X-ray powder diffraction (XRD), Fourier transform infrared spectra, scanning electron microscope (SEM), TGA, and N(2) adsorption isotherms. The LC of M-MIL-100(Fe) and EE of ACF were determined. Nuclear magnetic resonance (NMR) and zeta-potential analyses were employed to confirm qualitatively the drug loading within M-MIL-100(Fe). RESULTS: The ACF LC of MIL-100(Fe) was 27%, whereas the LC of M-MIL-100(Fe) was significantly increased and ranged from 37% in Ca I-MIL-100(Fe) to about 57% and 59% in Mn II-MIL-100(Fe) and Zn II-MIL-100(Fe), respectively. The ACF@M-MOFs release profiles showed slow release rates in phosphate buffer solutions at pH 6.8 and 7.4 as compared to the ACF@MIL-100(Fe). CONCLUSION: Therefore, M-MOFs showed a significant potential as a carrier for drug delivery systems. Dove Medical Press 2018-12-18 /pmc/articles/PMC6305134/ /pubmed/30587925 http://dx.doi.org/10.2147/DDDT.S182983 Text en © 2019 Al Haydar 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 Al Haydar, Muder Abid, Hussein Rasool Sunderland, Bruce Wang, Shaobin Multimetal organic frameworks as drug carriers: aceclofenac as a drug candidate |
title | Multimetal organic frameworks as drug carriers: aceclofenac as a drug candidate |
title_full | Multimetal organic frameworks as drug carriers: aceclofenac as a drug candidate |
title_fullStr | Multimetal organic frameworks as drug carriers: aceclofenac as a drug candidate |
title_full_unstemmed | Multimetal organic frameworks as drug carriers: aceclofenac as a drug candidate |
title_short | Multimetal organic frameworks as drug carriers: aceclofenac as a drug candidate |
title_sort | multimetal organic frameworks as drug carriers: aceclofenac as a drug candidate |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6305134/ https://www.ncbi.nlm.nih.gov/pubmed/30587925 http://dx.doi.org/10.2147/DDDT.S182983 |
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