Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/121962
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dc.contributor.authorAl Haydar, M.-
dc.contributor.authorAbid, H.R.-
dc.contributor.authorSunderland, B.-
dc.contributor.authorWang, S.-
dc.date.issued2019-
dc.identifier.citationDrug Design, Development and Therapy, 2019; 13:23-35-
dc.identifier.issn1177-8881-
dc.identifier.issn1177-8881-
dc.identifier.urihttp://hdl.handle.net/2440/121962-
dc.description.abstractBackground: 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 N2 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.-
dc.description.statementofresponsibilityMuder Al Haydar, Hussein Rasool Abid, Bruce Sunderland, Shaobin Wang-
dc.language.isoen-
dc.publisherDove Medical Press-
dc.rights© 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. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).-
dc.source.urihttp://dx.doi.org/10.2147/dddt.s182983-
dc.subjectAceclofenac; mixed metal-MOF; MIL-100; drug delivery; drug loading-
dc.titleMultimetal organic frameworks as drug carriers: aceclofenac as a drug candidate-
dc.typeJournal article-
dc.identifier.doi10.2147/DDDT.S182983-
pubs.publication-statusPublished-
dc.identifier.orcidWang, S. [0000-0002-1751-9162]-
Appears in Collections:Aurora harvest 4
Chemical Engineering publications

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