Effect of magnetic and silica ratio on the synthesis of magnetic mesoporous silica particles
Mesoporous magnetic silica (MMS) particle can be developed as a material for theragnostic-agent. It can offer therapeutic ability through hyperthermia treatment and drug-carrying possibility, while the magnetic particle can also be expected as an MRI contrast agent for diagnostic purposes. An effect...
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creator | Prasetya, Ahadi Damar Fisli, Adel Sulungbudi, Grace Tj Richtiara, Gavrila Caesarissa Muslih, M. Refai Mujamilah Wildan, Z. L. Firda, Yurituna |
description | Mesoporous magnetic silica (MMS) particle can be developed as a material for theragnostic-agent. It can offer therapeutic ability through hyperthermia treatment and drug-carrying possibility, while the magnetic particle can also be expected as an MRI contrast agent for diagnostic purposes. An effective MMS theragnostic agent should have high magnetic moment, small size and high surface area. In this work, MMS was synthesized with a variation of the magnetic and silica ratio. The magnetic nanoparticle was synthesized first through the co-precipitation method. The synthesize of MMS was conducted with two variations of magnetic and silica ratio (MMS 1:1 and 2:1) and the porous system was formed during hydrolysis of CTAB at the controlled sintering process. The samples were characterized using FTIR, XRD, VSM, PSA, and nitrogen adsorption-desorption. The MMS 2:1 result shows a larger particle size (more than 300 nm), lower magnetic moment (25 emu/g) compared to the MMS 1:1 (less than 300 nm in particle size and 35 emu/g for the magnetic moment). The nitrogen adsorption-desorption isotherm profiles confirm the formation of a mesoporous structure with nearly the same pore diameter for the two samples but a higher surface area for MMS 1:1. Further analysis should be done to confirm the magnetic nanoparticle position the formation of the mesoporous structure of the materials. |
doi_str_mv | 10.1063/5.0066528 |
format | Conference Proceeding |
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Refai ; Mujamilah ; Wildan, Z. L. ; Firda, Yurituna</creator><contributor>Sugono, Irawan ; Mulyani, Emy ; Mujamilah ; Taufik ; Rifai, Muhammad ; Santoso, Muhayatun</contributor><creatorcontrib>Prasetya, Ahadi Damar ; Fisli, Adel ; Sulungbudi, Grace Tj ; Richtiara, Gavrila Caesarissa ; Muslih, M. Refai ; Mujamilah ; Wildan, Z. L. ; Firda, Yurituna ; Sugono, Irawan ; Mulyani, Emy ; Mujamilah ; Taufik ; Rifai, Muhammad ; Santoso, Muhayatun</creatorcontrib><description>Mesoporous magnetic silica (MMS) particle can be developed as a material for theragnostic-agent. It can offer therapeutic ability through hyperthermia treatment and drug-carrying possibility, while the magnetic particle can also be expected as an MRI contrast agent for diagnostic purposes. An effective MMS theragnostic agent should have high magnetic moment, small size and high surface area. In this work, MMS was synthesized with a variation of the magnetic and silica ratio. The magnetic nanoparticle was synthesized first through the co-precipitation method. The synthesize of MMS was conducted with two variations of magnetic and silica ratio (MMS 1:1 and 2:1) and the porous system was formed during hydrolysis of CTAB at the controlled sintering process. The samples were characterized using FTIR, XRD, VSM, PSA, and nitrogen adsorption-desorption. The MMS 2:1 result shows a larger particle size (more than 300 nm), lower magnetic moment (25 emu/g) compared to the MMS 1:1 (less than 300 nm in particle size and 35 emu/g for the magnetic moment). The nitrogen adsorption-desorption isotherm profiles confirm the formation of a mesoporous structure with nearly the same pore diameter for the two samples but a higher surface area for MMS 1:1. Further analysis should be done to confirm the magnetic nanoparticle position the formation of the mesoporous structure of the materials.</description><identifier>ISSN: 0094-243X</identifier><identifier>EISSN: 1551-7616</identifier><identifier>DOI: 10.1063/5.0066528</identifier><identifier>CODEN: APCPCS</identifier><language>eng</language><publisher>Melville: American Institute of Physics</publisher><subject>Adsorption ; Chemical compounds ; Contrast agents ; Desorption ; Hyperthermia ; Magnetic moments ; Nanoparticles ; Particle size ; Pharmacology ; Silicon dioxide ; Sintering (powder metallurgy) ; Surface area ; Surface chemistry ; Synthesis</subject><ispartof>AIP conference proceedings, 2021, Vol.2381 (1)</ispartof><rights>Author(s)</rights><rights>2021 Author(s). 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Refai</creatorcontrib><creatorcontrib>Mujamilah</creatorcontrib><creatorcontrib>Wildan, Z. L.</creatorcontrib><creatorcontrib>Firda, Yurituna</creatorcontrib><title>Effect of magnetic and silica ratio on the synthesis of magnetic mesoporous silica particles</title><title>AIP conference proceedings</title><description>Mesoporous magnetic silica (MMS) particle can be developed as a material for theragnostic-agent. It can offer therapeutic ability through hyperthermia treatment and drug-carrying possibility, while the magnetic particle can also be expected as an MRI contrast agent for diagnostic purposes. An effective MMS theragnostic agent should have high magnetic moment, small size and high surface area. In this work, MMS was synthesized with a variation of the magnetic and silica ratio. The magnetic nanoparticle was synthesized first through the co-precipitation method. The synthesize of MMS was conducted with two variations of magnetic and silica ratio (MMS 1:1 and 2:1) and the porous system was formed during hydrolysis of CTAB at the controlled sintering process. The samples were characterized using FTIR, XRD, VSM, PSA, and nitrogen adsorption-desorption. The MMS 2:1 result shows a larger particle size (more than 300 nm), lower magnetic moment (25 emu/g) compared to the MMS 1:1 (less than 300 nm in particle size and 35 emu/g for the magnetic moment). The nitrogen adsorption-desorption isotherm profiles confirm the formation of a mesoporous structure with nearly the same pore diameter for the two samples but a higher surface area for MMS 1:1. Further analysis should be done to confirm the magnetic nanoparticle position the formation of the mesoporous structure of the materials.</description><subject>Adsorption</subject><subject>Chemical compounds</subject><subject>Contrast agents</subject><subject>Desorption</subject><subject>Hyperthermia</subject><subject>Magnetic moments</subject><subject>Nanoparticles</subject><subject>Particle size</subject><subject>Pharmacology</subject><subject>Silicon dioxide</subject><subject>Sintering (powder metallurgy)</subject><subject>Surface area</subject><subject>Surface chemistry</subject><subject>Synthesis</subject><issn>0094-243X</issn><issn>1551-7616</issn><fulltext>true</fulltext><rsrctype>conference_proceeding</rsrctype><creationdate>2021</creationdate><recordtype>conference_proceeding</recordtype><recordid>eNp9kE1LAzEQhoMoWKsH_0HAm7B1kmw2yVFK_YCCFwUPQshmE01pN2uyK_Tfu6UV8eLpPczzzjAPQpcEZgQqdsNnAFXFqTxCE8I5KURFqmM0AVBlQUv2eorOcl4BUCWEnKC3hffO9jh6vDHvreuDxaZtcA7rYA1Opg8Rxxb3Hw7nbTtGDvkPvXE5djHFIf-UOpPGwdrlc3TizTq7i0NO0cvd4nn-UCyf7h_nt8uio8BkUVelbKitvbWsboyrnWQehDFQCwOKEKW8EpYqphrORWlK4sDIxjoQjtaWTdHVfm-X4ufgcq9XcUjteFJTrkYBRFIxUtd7KtvQ7_5qdZfCxqSt_opJc30wp7vG_wcT0DvVvwX2DQiYcZs</recordid><startdate>20211111</startdate><enddate>20211111</enddate><creator>Prasetya, Ahadi Damar</creator><creator>Fisli, Adel</creator><creator>Sulungbudi, Grace Tj</creator><creator>Richtiara, Gavrila Caesarissa</creator><creator>Muslih, M. Refai</creator><creator>Mujamilah</creator><creator>Wildan, Z. L.</creator><creator>Firda, Yurituna</creator><general>American Institute of Physics</general><scope>8FD</scope><scope>H8D</scope><scope>L7M</scope></search><sort><creationdate>20211111</creationdate><title>Effect of magnetic and silica ratio on the synthesis of magnetic mesoporous silica particles</title><author>Prasetya, Ahadi Damar ; Fisli, Adel ; Sulungbudi, Grace Tj ; Richtiara, Gavrila Caesarissa ; Muslih, M. Refai ; Mujamilah ; Wildan, Z. L. ; Firda, Yurituna</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p2038-b648d2cbfcc3bdaebe83f07aa0b7a091199f97c2939d5574a41e0a8dce07e2bc3</frbrgroupid><rsrctype>conference_proceedings</rsrctype><prefilter>conference_proceedings</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Adsorption</topic><topic>Chemical compounds</topic><topic>Contrast agents</topic><topic>Desorption</topic><topic>Hyperthermia</topic><topic>Magnetic moments</topic><topic>Nanoparticles</topic><topic>Particle size</topic><topic>Pharmacology</topic><topic>Silicon dioxide</topic><topic>Sintering (powder metallurgy)</topic><topic>Surface area</topic><topic>Surface chemistry</topic><topic>Synthesis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Prasetya, Ahadi Damar</creatorcontrib><creatorcontrib>Fisli, Adel</creatorcontrib><creatorcontrib>Sulungbudi, Grace Tj</creatorcontrib><creatorcontrib>Richtiara, Gavrila Caesarissa</creatorcontrib><creatorcontrib>Muslih, M. Refai</creatorcontrib><creatorcontrib>Mujamilah</creatorcontrib><creatorcontrib>Wildan, Z. L.</creatorcontrib><creatorcontrib>Firda, Yurituna</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>Prasetya, Ahadi Damar</au><au>Fisli, Adel</au><au>Sulungbudi, Grace Tj</au><au>Richtiara, Gavrila Caesarissa</au><au>Muslih, M. Refai</au><au>Mujamilah</au><au>Wildan, Z. L.</au><au>Firda, Yurituna</au><au>Sugono, Irawan</au><au>Mulyani, Emy</au><au>Mujamilah</au><au>Taufik</au><au>Rifai, Muhammad</au><au>Santoso, Muhayatun</au><format>book</format><genre>proceeding</genre><ristype>CONF</ristype><atitle>Effect of magnetic and silica ratio on the synthesis of magnetic mesoporous silica particles</atitle><btitle>AIP conference proceedings</btitle><date>2021-11-11</date><risdate>2021</risdate><volume>2381</volume><issue>1</issue><issn>0094-243X</issn><eissn>1551-7616</eissn><coden>APCPCS</coden><abstract>Mesoporous magnetic silica (MMS) particle can be developed as a material for theragnostic-agent. It can offer therapeutic ability through hyperthermia treatment and drug-carrying possibility, while the magnetic particle can also be expected as an MRI contrast agent for diagnostic purposes. An effective MMS theragnostic agent should have high magnetic moment, small size and high surface area. In this work, MMS was synthesized with a variation of the magnetic and silica ratio. The magnetic nanoparticle was synthesized first through the co-precipitation method. The synthesize of MMS was conducted with two variations of magnetic and silica ratio (MMS 1:1 and 2:1) and the porous system was formed during hydrolysis of CTAB at the controlled sintering process. The samples were characterized using FTIR, XRD, VSM, PSA, and nitrogen adsorption-desorption. The MMS 2:1 result shows a larger particle size (more than 300 nm), lower magnetic moment (25 emu/g) compared to the MMS 1:1 (less than 300 nm in particle size and 35 emu/g for the magnetic moment). The nitrogen adsorption-desorption isotherm profiles confirm the formation of a mesoporous structure with nearly the same pore diameter for the two samples but a higher surface area for MMS 1:1. Further analysis should be done to confirm the magnetic nanoparticle position the formation of the mesoporous structure of the materials.</abstract><cop>Melville</cop><pub>American Institute of Physics</pub><doi>10.1063/5.0066528</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adsorption Chemical compounds Contrast agents Desorption Hyperthermia Magnetic moments Nanoparticles Particle size Pharmacology Silicon dioxide Sintering (powder metallurgy) Surface area Surface chemistry Synthesis |
title | Effect of magnetic and silica ratio on the synthesis of magnetic mesoporous silica particles |
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