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Extended release of 6-aminopenicillanic acid by silanol group functionalized vermiculite
The present study aimed to improve capability of vermiculite for extended release ofdrug such as: 6-Aminopenicillanic acid (6-APA). For this purpose, functionalization of vermiculite (VMT) was done by utilizing silanol through hydrolyzing of tetraethoxysilane. The synthesized samples characterized t...
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Published in: | Journal of dispersion science and technology 2022-06, Vol.43 (8), p.1231-1244 |
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creator | Soleimanpour Moghadam, Nona Azadmehr, Amirreza Hezarkhani, Ardeshir |
description | The present study aimed to improve capability of vermiculite for extended release ofdrug such as: 6-Aminopenicillanic acid (6-APA). For this purpose, functionalization of vermiculite (VMT) was done by utilizing silanol through hydrolyzing of tetraethoxysilane. The synthesized samples characterized through the XRD, FTIR and BET analyses. The Maximum obtained 6-APA absorption capacity of VMT-Si was 243.9 mg/g, which was higher than other clays. The equilibrium studies demonstrate that drug absorption on VMT and VMT-Si is homogeneous and heterogeneous, respectively. Kinetic studies have been performed by applying reaction based models (such as: pseudo-first-order and pseudo-second-order) and diffusion based models (such as: Boyd, intra-particle diffusion and mass transfer models), which indicates the chemisorption interaction of both aforementioned compounds. The in-vitro release profile of VMT showed a release of about 52% after 5 hours. Whereas, the in-vitro release profile of 6-APA from VMT-Si showed substantially less release of 70% after 7 hours compare to VMT. The maximum obtained release amount of antibiotic (6-APA) per each gram of VMT-Si-6APA and VMT-6APA was 167 mg and 45 mg, respectively. Release kinetic studies show that the release mechanism of 6-APA is controlled by the diffusion process based on Fick's law. In conclusion, vermiculite functionalization with silanol, reduced the rate of drug release and increased the amount of released 6-APA. |
doi_str_mv | 10.1080/01932691.2020.1850291 |
format | article |
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For this purpose, functionalization of vermiculite (VMT) was done by utilizing silanol through hydrolyzing of tetraethoxysilane. The synthesized samples characterized through the XRD, FTIR and BET analyses. The Maximum obtained 6-APA absorption capacity of VMT-Si was 243.9 mg/g, which was higher than other clays. The equilibrium studies demonstrate that drug absorption on VMT and VMT-Si is homogeneous and heterogeneous, respectively. Kinetic studies have been performed by applying reaction based models (such as: pseudo-first-order and pseudo-second-order) and diffusion based models (such as: Boyd, intra-particle diffusion and mass transfer models), which indicates the chemisorption interaction of both aforementioned compounds. The in-vitro release profile of VMT showed a release of about 52% after 5 hours. Whereas, the in-vitro release profile of 6-APA from VMT-Si showed substantially less release of 70% after 7 hours compare to VMT. The maximum obtained release amount of antibiotic (6-APA) per each gram of VMT-Si-6APA and VMT-6APA was 167 mg and 45 mg, respectively. Release kinetic studies show that the release mechanism of 6-APA is controlled by the diffusion process based on Fick's law. In conclusion, vermiculite functionalization with silanol, reduced the rate of drug release and increased the amount of released 6-APA.</description><identifier>ISSN: 0193-2691</identifier><identifier>EISSN: 1532-2351</identifier><identifier>DOI: 10.1080/01932691.2020.1850291</identifier><language>eng</language><publisher>Philadelphia: Taylor & Francis</publisher><subject>6-aminopenicillanic acid ; Absorption ; Aminopenicillanic acid ; Antibiotics ; Chemisorption ; drug delivery ; equilibrium and kinetic studies ; Mass transfer ; Particle diffusion ; Tetraethyl orthosilicate ; Vermiculite</subject><ispartof>Journal of dispersion science and technology, 2022-06, Vol.43 (8), p.1231-1244</ispartof><rights>2021 Taylor & Francis Group, LLC 2021</rights><rights>2021 Taylor & Francis Group, LLC</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c338t-4e2f47587d0d4b41e3c4541322f8d373cbb52e69fc8f0ab582a052ef81608e73</citedby><cites>FETCH-LOGICAL-c338t-4e2f47587d0d4b41e3c4541322f8d373cbb52e69fc8f0ab582a052ef81608e73</cites><orcidid>0000-0002-1149-3440</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Soleimanpour Moghadam, Nona</creatorcontrib><creatorcontrib>Azadmehr, Amirreza</creatorcontrib><creatorcontrib>Hezarkhani, Ardeshir</creatorcontrib><title>Extended release of 6-aminopenicillanic acid by silanol group functionalized vermiculite</title><title>Journal of dispersion science and technology</title><description>The present study aimed to improve capability of vermiculite for extended release ofdrug such as: 6-Aminopenicillanic acid (6-APA). For this purpose, functionalization of vermiculite (VMT) was done by utilizing silanol through hydrolyzing of tetraethoxysilane. The synthesized samples characterized through the XRD, FTIR and BET analyses. The Maximum obtained 6-APA absorption capacity of VMT-Si was 243.9 mg/g, which was higher than other clays. The equilibrium studies demonstrate that drug absorption on VMT and VMT-Si is homogeneous and heterogeneous, respectively. Kinetic studies have been performed by applying reaction based models (such as: pseudo-first-order and pseudo-second-order) and diffusion based models (such as: Boyd, intra-particle diffusion and mass transfer models), which indicates the chemisorption interaction of both aforementioned compounds. The in-vitro release profile of VMT showed a release of about 52% after 5 hours. Whereas, the in-vitro release profile of 6-APA from VMT-Si showed substantially less release of 70% after 7 hours compare to VMT. The maximum obtained release amount of antibiotic (6-APA) per each gram of VMT-Si-6APA and VMT-6APA was 167 mg and 45 mg, respectively. Release kinetic studies show that the release mechanism of 6-APA is controlled by the diffusion process based on Fick's law. In conclusion, vermiculite functionalization with silanol, reduced the rate of drug release and increased the amount of released 6-APA.</description><subject>6-aminopenicillanic acid</subject><subject>Absorption</subject><subject>Aminopenicillanic acid</subject><subject>Antibiotics</subject><subject>Chemisorption</subject><subject>drug delivery</subject><subject>equilibrium and kinetic studies</subject><subject>Mass transfer</subject><subject>Particle diffusion</subject><subject>Tetraethyl orthosilicate</subject><subject>Vermiculite</subject><issn>0193-2691</issn><issn>1532-2351</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp9kEtLxDAUhYMoOD5-ghBw3TGPpk13yjA-YMDNLNyFNE0kQ5rUpFXHX2_KjFtXl3P4zuFyALjBaIkRR3cIN5RUDV4SRLLFGSINPgELzCgpCGX4FCxmppihc3CR0g5lXSO-AG_r71H7Tncwaqdl0jAYWBWytz4M2ltlnZP5QKlsB9s9TDbr4OB7DNMAzeTVaIOXzv7kjk8de6smZ0d9Bc6MdElfH-8l2D6ut6vnYvP69LJ62BSKUj4WpSamrBmvO9SVbYk1VSUrMSXE8I7WVLUtI7pqjOIGyZZxIlE2DMcV4rqml-D2UDvE8DHpNIpdmGL-JwlS1YQzQqoyU-xAqRhSitqIIdpexr3ASMwbir8NxbyhOG6Yc_eHnPUmxF5-heg6Mcq9C9FE6ZVNgv5f8Qs0E3ij</recordid><startdate>20220615</startdate><enddate>20220615</enddate><creator>Soleimanpour Moghadam, Nona</creator><creator>Azadmehr, Amirreza</creator><creator>Hezarkhani, Ardeshir</creator><general>Taylor & Francis</general><general>Taylor & Francis Ltd</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7U5</scope><scope>8FD</scope><scope>L7M</scope><orcidid>https://orcid.org/0000-0002-1149-3440</orcidid></search><sort><creationdate>20220615</creationdate><title>Extended release of 6-aminopenicillanic acid by silanol group functionalized vermiculite</title><author>Soleimanpour Moghadam, Nona ; Azadmehr, Amirreza ; Hezarkhani, Ardeshir</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c338t-4e2f47587d0d4b41e3c4541322f8d373cbb52e69fc8f0ab582a052ef81608e73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>6-aminopenicillanic acid</topic><topic>Absorption</topic><topic>Aminopenicillanic acid</topic><topic>Antibiotics</topic><topic>Chemisorption</topic><topic>drug delivery</topic><topic>equilibrium and kinetic studies</topic><topic>Mass transfer</topic><topic>Particle diffusion</topic><topic>Tetraethyl orthosilicate</topic><topic>Vermiculite</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Soleimanpour Moghadam, Nona</creatorcontrib><creatorcontrib>Azadmehr, Amirreza</creatorcontrib><creatorcontrib>Hezarkhani, Ardeshir</creatorcontrib><collection>CrossRef</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Journal of dispersion science and technology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Soleimanpour Moghadam, Nona</au><au>Azadmehr, Amirreza</au><au>Hezarkhani, Ardeshir</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Extended release of 6-aminopenicillanic acid by silanol group functionalized vermiculite</atitle><jtitle>Journal of dispersion science and technology</jtitle><date>2022-06-15</date><risdate>2022</risdate><volume>43</volume><issue>8</issue><spage>1231</spage><epage>1244</epage><pages>1231-1244</pages><issn>0193-2691</issn><eissn>1532-2351</eissn><abstract>The present study aimed to improve capability of vermiculite for extended release ofdrug such as: 6-Aminopenicillanic acid (6-APA). For this purpose, functionalization of vermiculite (VMT) was done by utilizing silanol through hydrolyzing of tetraethoxysilane. The synthesized samples characterized through the XRD, FTIR and BET analyses. The Maximum obtained 6-APA absorption capacity of VMT-Si was 243.9 mg/g, which was higher than other clays. The equilibrium studies demonstrate that drug absorption on VMT and VMT-Si is homogeneous and heterogeneous, respectively. Kinetic studies have been performed by applying reaction based models (such as: pseudo-first-order and pseudo-second-order) and diffusion based models (such as: Boyd, intra-particle diffusion and mass transfer models), which indicates the chemisorption interaction of both aforementioned compounds. The in-vitro release profile of VMT showed a release of about 52% after 5 hours. Whereas, the in-vitro release profile of 6-APA from VMT-Si showed substantially less release of 70% after 7 hours compare to VMT. The maximum obtained release amount of antibiotic (6-APA) per each gram of VMT-Si-6APA and VMT-6APA was 167 mg and 45 mg, respectively. Release kinetic studies show that the release mechanism of 6-APA is controlled by the diffusion process based on Fick's law. In conclusion, vermiculite functionalization with silanol, reduced the rate of drug release and increased the amount of released 6-APA.</abstract><cop>Philadelphia</cop><pub>Taylor & Francis</pub><doi>10.1080/01932691.2020.1850291</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0002-1149-3440</orcidid></addata></record> |
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subjects | 6-aminopenicillanic acid Absorption Aminopenicillanic acid Antibiotics Chemisorption drug delivery equilibrium and kinetic studies Mass transfer Particle diffusion Tetraethyl orthosilicate Vermiculite |
title | Extended release of 6-aminopenicillanic acid by silanol group functionalized vermiculite |
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