Preparation of Magadiite-Sodium Alginate Drug Carrier Composite by Pickering-Emulsion-Templated-Encapsulation Method and Its Properties of Sustained Release Mechanism by Baker–Lonsdale and Korsmeyer–Peppas Model
In this study, the nanohybrid drug carrier were synthesized by Pickering emulsion-templated encapsulation (PETE) method to control the sustained-released properties of the nanohybrid drug carrier; magadiite-cetyltriphenyl phosphonium bromide (MAG-CTPB-KH550) and sodium alginate (NaC 6 H 7 O 6 ) was...
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| Veröffentlicht in: | Journal of polymers and the environment 2022-09, Vol.30 (9), p.3890-3900 |
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| container_title | Journal of polymers and the environment |
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| creator | Ge, Mingliang Li, Xinxiang Li, Yueying Jahangir Alam, S. M. Gui, Yuee Huang, Yongchao Cao, Luoxiang Liang, Guodong Hu, Guoqing |
| description | In this study, the nanohybrid drug carrier were synthesized by Pickering emulsion-templated encapsulation (PETE) method to control the sustained-released properties of the nanohybrid drug carrier; magadiite-cetyltriphenyl phosphonium bromide (MAG-CTPB-KH550) and sodium alginate (NaC
6
H
7
O
6
) was dissolved in the aqueous phase but metronidazole (C
6
H
9
N
3
O
3
) was dissolved in the ethyl acetate (CH
3
COOC
2
H
5
) of the oil phase; both the oil phase and the aqueous phase were mixed and dispersed to prepared organically-modified magadiite-sodium alginate (MAG–CTPB–KH550/SA) nanohybrid drug carrier. X-ray diffraction (XRD), Flourier transform infrared spectrometry (FTIR) and scanning electron microscopy (SEM) results were shown that the most of Sodium alginate (SA) were encapsulated into the MAG–CTPB–KH550 but a few of SA were intercalated into the inner space layers of MAG–CTPB–KH550, metronidazole was combined with carrier materials through physical apparent adsorption, ion exchange and electrostatic interaction. In vitro result, it was showed that the slow release was shown less than 10% content of Sodium alginate; whereas, it was reduced the initial release percentage of Metronidazole but it was extended the sustained-released time. To reach at equilibrium, the sustained-released effects of the drug carrier were prepared with 10% of Sodium Alginate for 32 h and the maximum cumulative release percentage was 93.42% for 24 h. First order model, Baker–Lonsdale model and Korsmeyer–Peppas model were fitted to study the slow-release mechanism; the correlation coefficients (R
2
) of the three models were found over 0.9; thus, it was well described the release kinetics behavior of drug carrier composites. The slow-release mechanisms of the drug carrier were performed swelling and dissolving but the barrier effects of the lamina that were reduced the dissolution percentage of metronidazole.
Graphical Abstract |
| doi_str_mv | 10.1007/s10924-022-02426-0 |
| format | Article |
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6
H
7
O
6
) was dissolved in the aqueous phase but metronidazole (C
6
H
9
N
3
O
3
) was dissolved in the ethyl acetate (CH
3
COOC
2
H
5
) of the oil phase; both the oil phase and the aqueous phase were mixed and dispersed to prepared organically-modified magadiite-sodium alginate (MAG–CTPB–KH550/SA) nanohybrid drug carrier. X-ray diffraction (XRD), Flourier transform infrared spectrometry (FTIR) and scanning electron microscopy (SEM) results were shown that the most of Sodium alginate (SA) were encapsulated into the MAG–CTPB–KH550 but a few of SA were intercalated into the inner space layers of MAG–CTPB–KH550, metronidazole was combined with carrier materials through physical apparent adsorption, ion exchange and electrostatic interaction. In vitro result, it was showed that the slow release was shown less than 10% content of Sodium alginate; whereas, it was reduced the initial release percentage of Metronidazole but it was extended the sustained-released time. To reach at equilibrium, the sustained-released effects of the drug carrier were prepared with 10% of Sodium Alginate for 32 h and the maximum cumulative release percentage was 93.42% for 24 h. First order model, Baker–Lonsdale model and Korsmeyer–Peppas model were fitted to study the slow-release mechanism; the correlation coefficients (R
2
) of the three models were found over 0.9; thus, it was well described the release kinetics behavior of drug carrier composites. The slow-release mechanisms of the drug carrier were performed swelling and dissolving but the barrier effects of the lamina that were reduced the dissolution percentage of metronidazole.
Graphical Abstract</description><identifier>ISSN: 1566-2543</identifier><identifier>EISSN: 1572-8919</identifier><identifier>DOI: 10.1007/s10924-022-02426-0</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Acetic acid ; Alginic acid ; Chemistry ; Chemistry and Materials Science ; Control methods ; Controlled release ; Correlation coefficient ; Correlation coefficients ; Dissolution ; Drug carriers ; Drug delivery ; Electrostatic properties ; Emulsions ; Encapsulation ; Environmental Chemistry ; Environmental Engineering/Biotechnology ; Ethyl acetate ; Industrial Chemistry/Chemical Engineering ; Infrared spectroscopy ; Ion exchange ; Materials Science ; Metronidazole ; Original Paper ; Polymer Sciences ; Scanning electron microscopy ; Sodium ; Sodium alginate ; Spectrometry ; Sustained release ; X-ray diffraction</subject><ispartof>Journal of polymers and the environment, 2022-09, Vol.30 (9), p.3890-3900</ispartof><rights>The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2022</rights><rights>The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2022.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c293t-bcd3bde129edf77b6a064f5ea868ef27d622cf3942df41e4aad0b394da651c923</citedby><cites>FETCH-LOGICAL-c293t-bcd3bde129edf77b6a064f5ea868ef27d622cf3942df41e4aad0b394da651c923</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10924-022-02426-0$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10924-022-02426-0$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids></links><search><creatorcontrib>Ge, Mingliang</creatorcontrib><creatorcontrib>Li, Xinxiang</creatorcontrib><creatorcontrib>Li, Yueying</creatorcontrib><creatorcontrib>Jahangir Alam, S. M.</creatorcontrib><creatorcontrib>Gui, Yuee</creatorcontrib><creatorcontrib>Huang, Yongchao</creatorcontrib><creatorcontrib>Cao, Luoxiang</creatorcontrib><creatorcontrib>Liang, Guodong</creatorcontrib><creatorcontrib>Hu, Guoqing</creatorcontrib><title>Preparation of Magadiite-Sodium Alginate Drug Carrier Composite by Pickering-Emulsion-Templated-Encapsulation Method and Its Properties of Sustained Release Mechanism by Baker–Lonsdale and Korsmeyer–Peppas Model</title><title>Journal of polymers and the environment</title><addtitle>J Polym Environ</addtitle><description>In this study, the nanohybrid drug carrier were synthesized by Pickering emulsion-templated encapsulation (PETE) method to control the sustained-released properties of the nanohybrid drug carrier; magadiite-cetyltriphenyl phosphonium bromide (MAG-CTPB-KH550) and sodium alginate (NaC
6
H
7
O
6
) was dissolved in the aqueous phase but metronidazole (C
6
H
9
N
3
O
3
) was dissolved in the ethyl acetate (CH
3
COOC
2
H
5
) of the oil phase; both the oil phase and the aqueous phase were mixed and dispersed to prepared organically-modified magadiite-sodium alginate (MAG–CTPB–KH550/SA) nanohybrid drug carrier. X-ray diffraction (XRD), Flourier transform infrared spectrometry (FTIR) and scanning electron microscopy (SEM) results were shown that the most of Sodium alginate (SA) were encapsulated into the MAG–CTPB–KH550 but a few of SA were intercalated into the inner space layers of MAG–CTPB–KH550, metronidazole was combined with carrier materials through physical apparent adsorption, ion exchange and electrostatic interaction. In vitro result, it was showed that the slow release was shown less than 10% content of Sodium alginate; whereas, it was reduced the initial release percentage of Metronidazole but it was extended the sustained-released time. To reach at equilibrium, the sustained-released effects of the drug carrier were prepared with 10% of Sodium Alginate for 32 h and the maximum cumulative release percentage was 93.42% for 24 h. First order model, Baker–Lonsdale model and Korsmeyer–Peppas model were fitted to study the slow-release mechanism; the correlation coefficients (R
2
) of the three models were found over 0.9; thus, it was well described the release kinetics behavior of drug carrier composites. The slow-release mechanisms of the drug carrier were performed swelling and dissolving but the barrier effects of the lamina that were reduced the dissolution percentage of metronidazole.
Graphical Abstract</description><subject>Acetic acid</subject><subject>Alginic acid</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Control methods</subject><subject>Controlled release</subject><subject>Correlation coefficient</subject><subject>Correlation coefficients</subject><subject>Dissolution</subject><subject>Drug carriers</subject><subject>Drug delivery</subject><subject>Electrostatic properties</subject><subject>Emulsions</subject><subject>Encapsulation</subject><subject>Environmental Chemistry</subject><subject>Environmental Engineering/Biotechnology</subject><subject>Ethyl acetate</subject><subject>Industrial Chemistry/Chemical Engineering</subject><subject>Infrared spectroscopy</subject><subject>Ion exchange</subject><subject>Materials Science</subject><subject>Metronidazole</subject><subject>Original Paper</subject><subject>Polymer Sciences</subject><subject>Scanning electron microscopy</subject><subject>Sodium</subject><subject>Sodium alginate</subject><subject>Spectrometry</subject><subject>Sustained release</subject><subject>X-ray diffraction</subject><issn>1566-2543</issn><issn>1572-8919</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kc1u1DAUhSNEJUrpC7CyxNpgO3-TZRkGqJgRo_6srZv4ZuqSxMY3WcyOd-Dhuu-T4EyQ2LGwrq17zvkknyR5K8V7KUT5gaSoVMaFUvFkquDiRXIu81LxVSWrl_O9KLjKs_RV8proUQhRReN58rQP6CHAaN3AXMt2cABj7Yj81hk79eyqO9gBRmSfwnRgawjBYmBr13tHUcbqI9vb5gcGOxz4pp86ikn8DnvfRZfhm6EBT1O3EHY4PjjDYDDseiS2D85jGC3SzL6daAQ7oGE32CEQRnnzAIOlfsZ8hEh5_vV76wYy0OEp5ZsL1OPxtNij90Bs5wx2b5KzFjrCy7_zIrn_vLlbf-Xb71-u11db3qgqHXndmLQ2KFWFpi3LugBRZG2OsCpW2KrSFEo1bVplyrSZxAzAiDo-DRS5bCqVXiTvllwf3M8JadSPbgpDRGpVCpkqleZpVKlF1QRHFLDVPtgewlFLoecC9VKgjgXqU4FaRFO6mMjPn4vhX_R_XH8AUFWlwA</recordid><startdate>20220901</startdate><enddate>20220901</enddate><creator>Ge, Mingliang</creator><creator>Li, Xinxiang</creator><creator>Li, Yueying</creator><creator>Jahangir Alam, S. M.</creator><creator>Gui, Yuee</creator><creator>Huang, Yongchao</creator><creator>Cao, Luoxiang</creator><creator>Liang, Guodong</creator><creator>Hu, Guoqing</creator><general>Springer US</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7SR</scope><scope>7XB</scope><scope>88I</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>BKSAR</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>JG9</scope><scope>KB.</scope><scope>M2P</scope><scope>PATMY</scope><scope>PCBAR</scope><scope>PDBOC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PYCSY</scope><scope>Q9U</scope></search><sort><creationdate>20220901</creationdate><title>Preparation of Magadiite-Sodium Alginate Drug Carrier Composite by Pickering-Emulsion-Templated-Encapsulation Method and Its Properties of Sustained Release Mechanism by Baker–Lonsdale and Korsmeyer–Peppas Model</title><author>Ge, Mingliang ; Li, Xinxiang ; Li, Yueying ; Jahangir Alam, S. M. ; Gui, Yuee ; Huang, Yongchao ; Cao, Luoxiang ; Liang, Guodong ; Hu, Guoqing</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c293t-bcd3bde129edf77b6a064f5ea868ef27d622cf3942df41e4aad0b394da651c923</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Acetic acid</topic><topic>Alginic acid</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Control methods</topic><topic>Controlled release</topic><topic>Correlation coefficient</topic><topic>Correlation coefficients</topic><topic>Dissolution</topic><topic>Drug carriers</topic><topic>Drug delivery</topic><topic>Electrostatic properties</topic><topic>Emulsions</topic><topic>Encapsulation</topic><topic>Environmental Chemistry</topic><topic>Environmental Engineering/Biotechnology</topic><topic>Ethyl acetate</topic><topic>Industrial Chemistry/Chemical Engineering</topic><topic>Infrared spectroscopy</topic><topic>Ion exchange</topic><topic>Materials Science</topic><topic>Metronidazole</topic><topic>Original Paper</topic><topic>Polymer Sciences</topic><topic>Scanning electron microscopy</topic><topic>Sodium</topic><topic>Sodium alginate</topic><topic>Spectrometry</topic><topic>Sustained release</topic><topic>X-ray diffraction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ge, Mingliang</creatorcontrib><creatorcontrib>Li, Xinxiang</creatorcontrib><creatorcontrib>Li, Yueying</creatorcontrib><creatorcontrib>Jahangir Alam, S. M.</creatorcontrib><creatorcontrib>Gui, Yuee</creatorcontrib><creatorcontrib>Huang, Yongchao</creatorcontrib><creatorcontrib>Cao, Luoxiang</creatorcontrib><creatorcontrib>Liang, Guodong</creatorcontrib><creatorcontrib>Hu, Guoqing</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Engineered Materials Abstracts</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Earth, Atmospheric & Aquatic Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>Materials Research Database</collection><collection>Materials Science Database</collection><collection>Science Database</collection><collection>Environmental Science Database</collection><collection>Earth, Atmospheric & Aquatic Science Database</collection><collection>Materials Science Collection</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Environmental Science Collection</collection><collection>ProQuest Central Basic</collection><jtitle>Journal of polymers and the environment</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ge, Mingliang</au><au>Li, Xinxiang</au><au>Li, Yueying</au><au>Jahangir Alam, S. M.</au><au>Gui, Yuee</au><au>Huang, Yongchao</au><au>Cao, Luoxiang</au><au>Liang, Guodong</au><au>Hu, Guoqing</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Preparation of Magadiite-Sodium Alginate Drug Carrier Composite by Pickering-Emulsion-Templated-Encapsulation Method and Its Properties of Sustained Release Mechanism by Baker–Lonsdale and Korsmeyer–Peppas Model</atitle><jtitle>Journal of polymers and the environment</jtitle><stitle>J Polym Environ</stitle><date>2022-09-01</date><risdate>2022</risdate><volume>30</volume><issue>9</issue><spage>3890</spage><epage>3900</epage><pages>3890-3900</pages><issn>1566-2543</issn><eissn>1572-8919</eissn><abstract>In this study, the nanohybrid drug carrier were synthesized by Pickering emulsion-templated encapsulation (PETE) method to control the sustained-released properties of the nanohybrid drug carrier; magadiite-cetyltriphenyl phosphonium bromide (MAG-CTPB-KH550) and sodium alginate (NaC
6
H
7
O
6
) was dissolved in the aqueous phase but metronidazole (C
6
H
9
N
3
O
3
) was dissolved in the ethyl acetate (CH
3
COOC
2
H
5
) of the oil phase; both the oil phase and the aqueous phase were mixed and dispersed to prepared organically-modified magadiite-sodium alginate (MAG–CTPB–KH550/SA) nanohybrid drug carrier. X-ray diffraction (XRD), Flourier transform infrared spectrometry (FTIR) and scanning electron microscopy (SEM) results were shown that the most of Sodium alginate (SA) were encapsulated into the MAG–CTPB–KH550 but a few of SA were intercalated into the inner space layers of MAG–CTPB–KH550, metronidazole was combined with carrier materials through physical apparent adsorption, ion exchange and electrostatic interaction. In vitro result, it was showed that the slow release was shown less than 10% content of Sodium alginate; whereas, it was reduced the initial release percentage of Metronidazole but it was extended the sustained-released time. To reach at equilibrium, the sustained-released effects of the drug carrier were prepared with 10% of Sodium Alginate for 32 h and the maximum cumulative release percentage was 93.42% for 24 h. First order model, Baker–Lonsdale model and Korsmeyer–Peppas model were fitted to study the slow-release mechanism; the correlation coefficients (R
2
) of the three models were found over 0.9; thus, it was well described the release kinetics behavior of drug carrier composites. The slow-release mechanisms of the drug carrier were performed swelling and dissolving but the barrier effects of the lamina that were reduced the dissolution percentage of metronidazole.
Graphical Abstract</abstract><cop>New York</cop><pub>Springer US</pub><doi>10.1007/s10924-022-02426-0</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 1566-2543 |
| ispartof | Journal of polymers and the environment, 2022-09, Vol.30 (9), p.3890-3900 |
| issn | 1566-2543 1572-8919 |
| language | eng |
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| source | SpringerNature Journals |
| subjects | Acetic acid Alginic acid Chemistry Chemistry and Materials Science Control methods Controlled release Correlation coefficient Correlation coefficients Dissolution Drug carriers Drug delivery Electrostatic properties Emulsions Encapsulation Environmental Chemistry Environmental Engineering/Biotechnology Ethyl acetate Industrial Chemistry/Chemical Engineering Infrared spectroscopy Ion exchange Materials Science Metronidazole Original Paper Polymer Sciences Scanning electron microscopy Sodium Sodium alginate Spectrometry Sustained release X-ray diffraction |
| title | Preparation of Magadiite-Sodium Alginate Drug Carrier Composite by Pickering-Emulsion-Templated-Encapsulation Method and Its Properties of Sustained Release Mechanism by Baker–Lonsdale and Korsmeyer–Peppas Model |
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