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Amino acid–intercalated layered double hydroxide core @ ordered porous silica shell as drug carriers: Design and applications
A nanoparticle-based drug delivery system is first established by mesoporous silica encapsulating amino acid–intercalated layered double hydroxide (LDH) to construct nanocomposites AA-LDH@MS. The amino acids including phenylalanine (Phe) and histidine (His) with aromatic groups are intercalated into...
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Published in: | Journal of materials research 2019-11, Vol.34 (22), p.3747-3756 |
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container_title | Journal of materials research |
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creator | Wang, Jianqiang Zhang, Wenpei Hao, Lifeng Sun, Jun Zhang, Wenqi Guo, Cheng Mu, Yuhan Ji, Weiting Yu, Caiyuan Yuan, Fangming |
description | A nanoparticle-based drug delivery system is first established by mesoporous silica encapsulating amino acid–intercalated layered double hydroxide (LDH) to construct nanocomposites AA-LDH@MS. The amino acids including phenylalanine (Phe) and histidine (His) with aromatic groups are intercalated into LDH as the cores Phe-LDH and His-LDH. These nanocomposites AA-LDH@MS display multispaces of the interlayer spaces of LDH and porous channels of mesoporous silica to load drugs. Moreover, amino acid molecules provide the interaction sites to improve effectively loading amounts of drugs. 5-Fluorouracil (5-FU) is used as the cargo molecules to observe the delivery in vitro. The results indicate that the maximum loading amounts of drugs are up to 392 mg/g at 60 °C for 12 h in the nanocomposite Phe-LDH@MS. All the nanocomposites exhibit the sustained release of 5-FU at pH 4 and pH 7.4. The Korsmeyer–Peppas model is used to fit the kinetic plot of the drug release in vitro, which concludes that 5-FU release from AA-LDH@MS belongs to Fickian diffusion. |
doi_str_mv | 10.1557/jmr.2019.324 |
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The amino acids including phenylalanine (Phe) and histidine (His) with aromatic groups are intercalated into LDH as the cores Phe-LDH and His-LDH. These nanocomposites AA-LDH@MS display multispaces of the interlayer spaces of LDH and porous channels of mesoporous silica to load drugs. Moreover, amino acid molecules provide the interaction sites to improve effectively loading amounts of drugs. 5-Fluorouracil (5-FU) is used as the cargo molecules to observe the delivery in vitro. The results indicate that the maximum loading amounts of drugs are up to 392 mg/g at 60 °C for 12 h in the nanocomposite Phe-LDH@MS. All the nanocomposites exhibit the sustained release of 5-FU at pH 4 and pH 7.4. The Korsmeyer–Peppas model is used to fit the kinetic plot of the drug release in vitro, which concludes that 5-FU release from AA-LDH@MS belongs to Fickian diffusion.</description><identifier>ISSN: 0884-2914</identifier><identifier>EISSN: 2044-5326</identifier><identifier>DOI: 10.1557/jmr.2019.324</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Amino acids ; Applied and Technical Physics ; Biocompatibility ; Biomaterials ; Biomedical Materials ; Drug carriers ; Drug delivery systems ; Fourier transforms ; Histidine ; Hydroxides ; Inorganic Chemistry ; Interlayers ; Materials Engineering ; Materials research ; Materials Science ; Nanocomposites ; Nanoparticles ; Nanotechnology ; Phenylalanine ; Regenerative Medicine and Drug Delivery ; Silicon dioxide ; Surfactants ; Sustained release</subject><ispartof>Journal of materials research, 2019-11, Vol.34 (22), p.3747-3756</ispartof><rights>The Materials Research Society 2019</rights><rights>Copyright © Materials Research Society 2019</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c338t-a23a063133c0784723bb9336adf41ec810071ce8124519eee2e25cd549f039f3</citedby><cites>FETCH-LOGICAL-c338t-a23a063133c0784723bb9336adf41ec810071ce8124519eee2e25cd549f039f3</cites><orcidid>0000-0002-0519-5690</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2338551126/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$H</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2338551126?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>315,786,790,11715,27957,27958,36095,44398,75252</link.rule.ids></links><search><creatorcontrib>Wang, Jianqiang</creatorcontrib><creatorcontrib>Zhang, Wenpei</creatorcontrib><creatorcontrib>Hao, Lifeng</creatorcontrib><creatorcontrib>Sun, Jun</creatorcontrib><creatorcontrib>Zhang, Wenqi</creatorcontrib><creatorcontrib>Guo, Cheng</creatorcontrib><creatorcontrib>Mu, Yuhan</creatorcontrib><creatorcontrib>Ji, Weiting</creatorcontrib><creatorcontrib>Yu, Caiyuan</creatorcontrib><creatorcontrib>Yuan, Fangming</creatorcontrib><title>Amino acid–intercalated layered double hydroxide core @ ordered porous silica shell as drug carriers: Design and applications</title><title>Journal of materials research</title><addtitle>Journal of Materials Research</addtitle><description>A nanoparticle-based drug delivery system is first established by mesoporous silica encapsulating amino acid–intercalated layered double hydroxide (LDH) to construct nanocomposites AA-LDH@MS. The amino acids including phenylalanine (Phe) and histidine (His) with aromatic groups are intercalated into LDH as the cores Phe-LDH and His-LDH. These nanocomposites AA-LDH@MS display multispaces of the interlayer spaces of LDH and porous channels of mesoporous silica to load drugs. Moreover, amino acid molecules provide the interaction sites to improve effectively loading amounts of drugs. 5-Fluorouracil (5-FU) is used as the cargo molecules to observe the delivery in vitro. The results indicate that the maximum loading amounts of drugs are up to 392 mg/g at 60 °C for 12 h in the nanocomposite Phe-LDH@MS. All the nanocomposites exhibit the sustained release of 5-FU at pH 4 and pH 7.4. The Korsmeyer–Peppas model is used to fit the kinetic plot of the drug release in vitro, which concludes that 5-FU release from AA-LDH@MS belongs to Fickian diffusion.</description><subject>Amino acids</subject><subject>Applied and Technical Physics</subject><subject>Biocompatibility</subject><subject>Biomaterials</subject><subject>Biomedical Materials</subject><subject>Drug carriers</subject><subject>Drug delivery systems</subject><subject>Fourier transforms</subject><subject>Histidine</subject><subject>Hydroxides</subject><subject>Inorganic Chemistry</subject><subject>Interlayers</subject><subject>Materials Engineering</subject><subject>Materials research</subject><subject>Materials Science</subject><subject>Nanocomposites</subject><subject>Nanoparticles</subject><subject>Nanotechnology</subject><subject>Phenylalanine</subject><subject>Regenerative Medicine and Drug Delivery</subject><subject>Silicon dioxide</subject><subject>Surfactants</subject><subject>Sustained release</subject><issn>0884-2914</issn><issn>2044-5326</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>M0C</sourceid><recordid>eNptkMtKw0AYhQdRsF52PsCAW1PnmosrS71CwU33YTrzp52SZuI_CdiVvoNv6JOYWsGNq7M4H-fAR8gFZ2OudXa93uBYMF6MpVAHZCSYUomWIj0kI5bnKhEFV8fkJMY1Y1yzTI3I-2Tjm0CN9e7r49M3HaA1tenA0dpsAYd0oV_UQFdbh-HNO6A2INBbGtD99G3A0Ecafe2toXEFdU1NpA77JbUG0QPGG3oH0S8bahpHTdvu0M6HJp6Ro8rUEc5_85TMH-7n06dk9vL4PJ3MEitl3iVGSMNSyaW0LMtVJuRiUUiZGlcpDjbnjGXcQs6F0rwAAAFCW6dVUTFZVPKUXO5nWwyvPcSuXIcem-GxFMOB1pyLdKCu9pTFECNCVbboNwa3JWflznA5GC53hsvB8IAnezwOWLME_Bv9l_8Gv8Z_yQ</recordid><startdate>20191128</startdate><enddate>20191128</enddate><creator>Wang, Jianqiang</creator><creator>Zhang, Wenpei</creator><creator>Hao, Lifeng</creator><creator>Sun, Jun</creator><creator>Zhang, Wenqi</creator><creator>Guo, Cheng</creator><creator>Mu, Yuhan</creator><creator>Ji, Weiting</creator><creator>Yu, Caiyuan</creator><creator>Yuan, 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hydroxide core @ ordered porous silica shell as drug carriers: Design and applications</title><author>Wang, Jianqiang ; Zhang, Wenpei ; Hao, Lifeng ; Sun, Jun ; Zhang, Wenqi ; Guo, Cheng ; Mu, Yuhan ; Ji, Weiting ; Yu, Caiyuan ; Yuan, Fangming</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c338t-a23a063133c0784723bb9336adf41ec810071ce8124519eee2e25cd549f039f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Amino acids</topic><topic>Applied and Technical Physics</topic><topic>Biocompatibility</topic><topic>Biomaterials</topic><topic>Biomedical Materials</topic><topic>Drug carriers</topic><topic>Drug delivery systems</topic><topic>Fourier transforms</topic><topic>Histidine</topic><topic>Hydroxides</topic><topic>Inorganic Chemistry</topic><topic>Interlayers</topic><topic>Materials Engineering</topic><topic>Materials research</topic><topic>Materials 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Research</stitle><date>2019-11-28</date><risdate>2019</risdate><volume>34</volume><issue>22</issue><spage>3747</spage><epage>3756</epage><pages>3747-3756</pages><issn>0884-2914</issn><eissn>2044-5326</eissn><abstract>A nanoparticle-based drug delivery system is first established by mesoporous silica encapsulating amino acid–intercalated layered double hydroxide (LDH) to construct nanocomposites AA-LDH@MS. The amino acids including phenylalanine (Phe) and histidine (His) with aromatic groups are intercalated into LDH as the cores Phe-LDH and His-LDH. These nanocomposites AA-LDH@MS display multispaces of the interlayer spaces of LDH and porous channels of mesoporous silica to load drugs. Moreover, amino acid molecules provide the interaction sites to improve effectively loading amounts of drugs. 5-Fluorouracil (5-FU) is used as the cargo molecules to observe the delivery in vitro. The results indicate that the maximum loading amounts of drugs are up to 392 mg/g at 60 °C for 12 h in the nanocomposite Phe-LDH@MS. All the nanocomposites exhibit the sustained release of 5-FU at pH 4 and pH 7.4. The Korsmeyer–Peppas model is used to fit the kinetic plot of the drug release in vitro, which concludes that 5-FU release from AA-LDH@MS belongs to Fickian diffusion.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><doi>10.1557/jmr.2019.324</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-0519-5690</orcidid></addata></record> |
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subjects | Amino acids Applied and Technical Physics Biocompatibility Biomaterials Biomedical Materials Drug carriers Drug delivery systems Fourier transforms Histidine Hydroxides Inorganic Chemistry Interlayers Materials Engineering Materials research Materials Science Nanocomposites Nanoparticles Nanotechnology Phenylalanine Regenerative Medicine and Drug Delivery Silicon dioxide Surfactants Sustained release |
title | Amino acid–intercalated layered double hydroxide core @ ordered porous silica shell as drug carriers: Design and applications |
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