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Synthesis and Functionalization of Porous Zr-Diaminostilbenedicarboxylate Metal–Organic Framework for Storage and Stable Delivery of Ibuprofen
[Image: see text] A stable porous metal–organic framework (MOF), Zr-diaminostilbenedicarboxylate (Zr-DASDCA), was synthesized and modified with oxalyl chloride (OC) or terephthaloyl chloride (TC) to introduce various functional groups onto the Zr-DASDCA. Both pristine and functionalized Zr-DASDCAs,...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6648809/ https://www.ncbi.nlm.nih.gov/pubmed/31460077 http://dx.doi.org/10.1021/acsomega.9b01139 |
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author | Sarker, Mithun Shin, Subin Jhung, Sung Hwa |
author_facet | Sarker, Mithun Shin, Subin Jhung, Sung Hwa |
author_sort | Sarker, Mithun |
collection | PubMed |
description | [Image: see text] A stable porous metal–organic framework (MOF), Zr-diaminostilbenedicarboxylate (Zr-DASDCA), was synthesized and modified with oxalyl chloride (OC) or terephthaloyl chloride (TC) to introduce various functional groups onto the Zr-DASDCA. Both pristine and functionalized Zr-DASDCAs, together with activated carbon, were used as a potential carrier for ibuprofen (IBU) storage and delivery. Zr-DASDCAs, especially the modified ones (OC-Zr-DASDCA and TC-Zr-DASDCA), showed competitive results in IBU delivery. Specifically, the release rate in phosphate-buffered saline solution at pH 7.4 was nearly constant (R(2) ≈ 0.98) for up to 10 days, which would be very effective in IBU dosing to the human body. Moreover, the release rate could be controlled by changing the pH of the releasing solution. The rate of IBU release from both pristine and modified Zr-DASDCAs at pH 7.4 and 3.0 was also explained with a few interactions such as H-bonding and electrostatic repulsion, together with the relative pore size of the Zr-DASDCAs. Therefore, the results suggested that functionalization of MOFs via postsynthetic modification, especially with OC and TC, to introduce various functional groups onto MOFs is an effective approach to not only reducing the release rate of IBU but also inducing a constant release of IBU for as long as 10 days. |
format | Online Article Text |
id | pubmed-6648809 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-66488092019-08-27 Synthesis and Functionalization of Porous Zr-Diaminostilbenedicarboxylate Metal–Organic Framework for Storage and Stable Delivery of Ibuprofen Sarker, Mithun Shin, Subin Jhung, Sung Hwa ACS Omega [Image: see text] A stable porous metal–organic framework (MOF), Zr-diaminostilbenedicarboxylate (Zr-DASDCA), was synthesized and modified with oxalyl chloride (OC) or terephthaloyl chloride (TC) to introduce various functional groups onto the Zr-DASDCA. Both pristine and functionalized Zr-DASDCAs, together with activated carbon, were used as a potential carrier for ibuprofen (IBU) storage and delivery. Zr-DASDCAs, especially the modified ones (OC-Zr-DASDCA and TC-Zr-DASDCA), showed competitive results in IBU delivery. Specifically, the release rate in phosphate-buffered saline solution at pH 7.4 was nearly constant (R(2) ≈ 0.98) for up to 10 days, which would be very effective in IBU dosing to the human body. Moreover, the release rate could be controlled by changing the pH of the releasing solution. The rate of IBU release from both pristine and modified Zr-DASDCAs at pH 7.4 and 3.0 was also explained with a few interactions such as H-bonding and electrostatic repulsion, together with the relative pore size of the Zr-DASDCAs. Therefore, the results suggested that functionalization of MOFs via postsynthetic modification, especially with OC and TC, to introduce various functional groups onto MOFs is an effective approach to not only reducing the release rate of IBU but also inducing a constant release of IBU for as long as 10 days. American Chemical Society 2019-06-05 /pmc/articles/PMC6648809/ /pubmed/31460077 http://dx.doi.org/10.1021/acsomega.9b01139 Text en Copyright © 2019 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Sarker, Mithun Shin, Subin Jhung, Sung Hwa Synthesis and Functionalization of Porous Zr-Diaminostilbenedicarboxylate Metal–Organic Framework for Storage and Stable Delivery of Ibuprofen |
title | Synthesis and Functionalization of Porous Zr-Diaminostilbenedicarboxylate
Metal–Organic Framework for Storage and Stable Delivery of
Ibuprofen |
title_full | Synthesis and Functionalization of Porous Zr-Diaminostilbenedicarboxylate
Metal–Organic Framework for Storage and Stable Delivery of
Ibuprofen |
title_fullStr | Synthesis and Functionalization of Porous Zr-Diaminostilbenedicarboxylate
Metal–Organic Framework for Storage and Stable Delivery of
Ibuprofen |
title_full_unstemmed | Synthesis and Functionalization of Porous Zr-Diaminostilbenedicarboxylate
Metal–Organic Framework for Storage and Stable Delivery of
Ibuprofen |
title_short | Synthesis and Functionalization of Porous Zr-Diaminostilbenedicarboxylate
Metal–Organic Framework for Storage and Stable Delivery of
Ibuprofen |
title_sort | synthesis and functionalization of porous zr-diaminostilbenedicarboxylate
metal–organic framework for storage and stable delivery of
ibuprofen |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6648809/ https://www.ncbi.nlm.nih.gov/pubmed/31460077 http://dx.doi.org/10.1021/acsomega.9b01139 |
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