The effect of TEOS precursor and CTAB addition in the synthesis of magnetic mesoporous silica nanoparticles for drug delivery
Nanoscale drug delivery systems have been found to increase drug loading efficiency and avoid the body’s immune response. In this research, magnetic mesoporous nanosilica was developed as a drug carrier by utilizing Kulon Progo iron sand’s natural resources as the material. Magnetic mesoporous nanos...
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description | Nanoscale drug delivery systems have been found to increase drug loading efficiency and avoid the body’s immune response. In this research, magnetic mesoporous nanosilica was developed as a drug carrier by utilizing Kulon Progo iron sand’s natural resources as the material. Magnetic mesoporous nanosilica was synthesized by the coprecipitation method using NH4OH as the precipitant. The synthesis was carried out in three stages to see the effect of adding silica and surfactant at each stage. The first stage was Fe3O4 synthesis from iron sand. The second stage included the synthesis of Fe3O4@SiO2 by adding Tetraethyl Orthosilicate (TEOS) as the silica precursor. The last stage was the synthesis of Fe3O4@SiO2−CTAB, in which Cetyltrimethylammonium Bromide (CTAB) was the surfactant used. Each of the materials synthesized was characterized using X-Ray Diffraction (XRD) and Energy Dispersive X-Ray (EDX). The crystalline size calculation results using XRD data show that the particles are in nano size, the particle size of Fe3O4@SiO2−CTAB nanoparticles obtained 6.77 nm. Simultaneously, the % crystallinity also shows better crystal quality results after the addition of the two compounds. This influence can also be seen from the EDX analysis, where Fe decreases and new compositions, namely Si and Br, are present. |
doi_str_mv | 10.1063/5.0130951 |
format | Conference Proceeding |
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In this research, magnetic mesoporous nanosilica was developed as a drug carrier by utilizing Kulon Progo iron sand’s natural resources as the material. Magnetic mesoporous nanosilica was synthesized by the coprecipitation method using NH4OH as the precipitant. The synthesis was carried out in three stages to see the effect of adding silica and surfactant at each stage. The first stage was Fe3O4 synthesis from iron sand. The second stage included the synthesis of Fe3O4@SiO2 by adding Tetraethyl Orthosilicate (TEOS) as the silica precursor. The last stage was the synthesis of Fe3O4@SiO2−CTAB, in which Cetyltrimethylammonium Bromide (CTAB) was the surfactant used. Each of the materials synthesized was characterized using X-Ray Diffraction (XRD) and Energy Dispersive X-Ray (EDX). The crystalline size calculation results using XRD data show that the particles are in nano size, the particle size of Fe3O4@SiO2−CTAB nanoparticles obtained 6.77 nm. Simultaneously, the % crystallinity also shows better crystal quality results after the addition of the two compounds. This influence can also be seen from the EDX analysis, where Fe decreases and new compositions, namely Si and Br, are present.</description><identifier>ISSN: 0094-243X</identifier><identifier>EISSN: 1551-7616</identifier><identifier>DOI: 10.1063/5.0130951</identifier><identifier>CODEN: APCPCS</identifier><language>eng</language><publisher>Melville: American Institute of Physics</publisher><subject>Ammonium hydroxide ; Cetyltrimethylammonium bromide ; Drug carriers ; Drug delivery systems ; Iron oxides ; Nanoparticles ; Natural resources ; Precursors ; Sand ; Silicon dioxide ; Surfactants ; Synthesis ; Tetraethyl orthosilicate ; X-ray diffraction</subject><ispartof>AIP conference proceedings, 2023, Vol.2623 (1)</ispartof><rights>Author(s)</rights><rights>2023 Author(s). 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In this research, magnetic mesoporous nanosilica was developed as a drug carrier by utilizing Kulon Progo iron sand’s natural resources as the material. Magnetic mesoporous nanosilica was synthesized by the coprecipitation method using NH4OH as the precipitant. The synthesis was carried out in three stages to see the effect of adding silica and surfactant at each stage. The first stage was Fe3O4 synthesis from iron sand. The second stage included the synthesis of Fe3O4@SiO2 by adding Tetraethyl Orthosilicate (TEOS) as the silica precursor. The last stage was the synthesis of Fe3O4@SiO2−CTAB, in which Cetyltrimethylammonium Bromide (CTAB) was the surfactant used. Each of the materials synthesized was characterized using X-Ray Diffraction (XRD) and Energy Dispersive X-Ray (EDX). The crystalline size calculation results using XRD data show that the particles are in nano size, the particle size of Fe3O4@SiO2−CTAB nanoparticles obtained 6.77 nm. Simultaneously, the % crystallinity also shows better crystal quality results after the addition of the two compounds. This influence can also be seen from the EDX analysis, where Fe decreases and new compositions, namely Si and Br, are present.</description><subject>Ammonium hydroxide</subject><subject>Cetyltrimethylammonium bromide</subject><subject>Drug carriers</subject><subject>Drug delivery systems</subject><subject>Iron oxides</subject><subject>Nanoparticles</subject><subject>Natural resources</subject><subject>Precursors</subject><subject>Sand</subject><subject>Silicon dioxide</subject><subject>Surfactants</subject><subject>Synthesis</subject><subject>Tetraethyl orthosilicate</subject><subject>X-ray diffraction</subject><issn>0094-243X</issn><issn>1551-7616</issn><fulltext>true</fulltext><rsrctype>conference_proceeding</rsrctype><creationdate>2023</creationdate><recordtype>conference_proceeding</recordtype><recordid>eNotUM1LwzAcDaLgnB78DwLehM6kaZrmOIdfMNjBHryVNPllZnRJTVphB_93O7bTO7wv3kPonpIFJSV74gtCGZGcXqAZ5ZxmoqTlJZoRIossL9jXNbpJaUdILoWoZuiv_gYM1oIecLC4ftl84j6CHmMKEStv8KpePmNljBtc8Nh5PEyOdPATJJeOpr3aehicxntIoQ8xjAkn1zmtsFc-9CpOZAcJ2ynSxHGLDXTuF-LhFl1Z1SW4O-Mc1a8v9eo9W2_ePlbLddbLkmeMlkKrogVdVJoa03JgopXWqtYSRaQk0lSy0pK1QFtBi1yDJVpY3RZCcMPm6OEU28fwM0Iaml0Yo58am7ziXOS0qvikejypknaDOq5t-uj2Kh4aSprjuw1vzu-yf4c0bkg</recordid><startdate>20230823</startdate><enddate>20230823</enddate><creator>Oktaviani, Erika Dwi</creator><creator>Petrus, Himawan Tri Bayu Murti</creator><creator>Kusumastuti, Yuni</creator><general>American Institute of Physics</general><scope>8FD</scope><scope>H8D</scope><scope>L7M</scope></search><sort><creationdate>20230823</creationdate><title>The effect of TEOS precursor and CTAB addition in the synthesis of magnetic mesoporous silica nanoparticles for drug delivery</title><author>Oktaviani, Erika Dwi ; Petrus, Himawan Tri Bayu Murti ; Kusumastuti, Yuni</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p965-3167ca4bec48c1ddb5e37b9ffabf0a09909d898c93be1b7142cef0c7fcb4775d3</frbrgroupid><rsrctype>conference_proceedings</rsrctype><prefilter>conference_proceedings</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Ammonium hydroxide</topic><topic>Cetyltrimethylammonium bromide</topic><topic>Drug carriers</topic><topic>Drug delivery systems</topic><topic>Iron oxides</topic><topic>Nanoparticles</topic><topic>Natural resources</topic><topic>Precursors</topic><topic>Sand</topic><topic>Silicon dioxide</topic><topic>Surfactants</topic><topic>Synthesis</topic><topic>Tetraethyl orthosilicate</topic><topic>X-ray diffraction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Oktaviani, Erika Dwi</creatorcontrib><creatorcontrib>Petrus, Himawan Tri Bayu Murti</creatorcontrib><creatorcontrib>Kusumastuti, Yuni</creatorcontrib><collection>Technology Research Database</collection><collection>Aerospace Database</collection><collection>Advanced Technologies Database with Aerospace</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Oktaviani, Erika Dwi</au><au>Petrus, Himawan Tri Bayu Murti</au><au>Kusumastuti, Yuni</au><au>Yudistira, Hadi Teguh</au><au>Arif, Muhamad Fatikul</au><au>Febrina, Melany</au><format>book</format><genre>proceeding</genre><ristype>CONF</ristype><atitle>The effect of TEOS precursor and CTAB addition in the synthesis of magnetic mesoporous silica nanoparticles for drug delivery</atitle><btitle>AIP conference proceedings</btitle><date>2023-08-23</date><risdate>2023</risdate><volume>2623</volume><issue>1</issue><issn>0094-243X</issn><eissn>1551-7616</eissn><coden>APCPCS</coden><abstract>Nanoscale drug delivery systems have been found to increase drug loading efficiency and avoid the body’s immune response. In this research, magnetic mesoporous nanosilica was developed as a drug carrier by utilizing Kulon Progo iron sand’s natural resources as the material. Magnetic mesoporous nanosilica was synthesized by the coprecipitation method using NH4OH as the precipitant. The synthesis was carried out in three stages to see the effect of adding silica and surfactant at each stage. The first stage was Fe3O4 synthesis from iron sand. The second stage included the synthesis of Fe3O4@SiO2 by adding Tetraethyl Orthosilicate (TEOS) as the silica precursor. The last stage was the synthesis of Fe3O4@SiO2−CTAB, in which Cetyltrimethylammonium Bromide (CTAB) was the surfactant used. Each of the materials synthesized was characterized using X-Ray Diffraction (XRD) and Energy Dispersive X-Ray (EDX). The crystalline size calculation results using XRD data show that the particles are in nano size, the particle size of Fe3O4@SiO2−CTAB nanoparticles obtained 6.77 nm. Simultaneously, the % crystallinity also shows better crystal quality results after the addition of the two compounds. This influence can also be seen from the EDX analysis, where Fe decreases and new compositions, namely Si and Br, are present.</abstract><cop>Melville</cop><pub>American Institute of Physics</pub><doi>10.1063/5.0130951</doi><tpages>6</tpages></addata></record> |
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language | eng |
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source | AIP Journals Complete |
subjects | Ammonium hydroxide Cetyltrimethylammonium bromide Drug carriers Drug delivery systems Iron oxides Nanoparticles Natural resources Precursors Sand Silicon dioxide Surfactants Synthesis Tetraethyl orthosilicate X-ray diffraction |
title | The effect of TEOS precursor and CTAB addition in the synthesis of magnetic mesoporous silica nanoparticles for drug delivery |
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