Targeted therapeutic effect against the breast cancer cell line MCF-7 with a CuFe 2 O 4 /silica/cisplatin nanocomposite formulation
The combination of magnetic nanoparticles with a porous silica is a composite that has attracted significant attention for potential multifunctional theranostic applications. In this study, 30 wt % CuFe O was impregnated into a matrix of monodispersed spherical hydrophilic silica (HYPS) nanoparticle...
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Veröffentlicht in: | Beilstein journal of nanotechnology 2019-11, Vol.10, p.2217-2228 |
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creator | Jermy, B Rabindran Ravinayagam, Vijaya Alamoudi, Widyan A Almohazey, Dana Dafalla, Hatim Hussain Allehaibi, Lina Baykal, Abdulhadi Toprak, Muhammet S Somanathan, Thirunavukkarasu |
description | The combination of magnetic nanoparticles with a porous silica is a composite that has attracted significant attention for potential multifunctional theranostic applications. In this study, 30 wt % CuFe
O
was impregnated into a matrix of monodispersed spherical hydrophilic silica (HYPS) nanoparticles through a simple dry impregnation technique. The chemotherapy drug cisplatin was loaded through electrostatic equilibrium adsorption over 24 h in normal saline solution. The presence of cubic spinel CuFe
O
on HYPS was confirmed through powder X-ray diffraction (PXRD), Fourier transform infrared spectroscopy (FTIR) and diffuse reflectance UV-vis spectroscopy (DR UV-vis) analysis. The HYPS particles showed a surface area of 170 m
/g, pore size of 8.3 nm and pore volume of 0.35 cm
/g. The cisplatin/CuFe
O
/HYPS nanoformulation showed the accumulation of copper ferrite nanoparticles on the surface and in the pores of HYPS with a surface area of 45 m
/g, pore size of 16 nm and pore volume of 0.18 cm
/g. Transmission electron microscopy (TEM) and energy dispersive X-ray (EDX) mapping analysis showed the presence of homogeneous silica particles with nanoclusters of copper ferrite distributed on the HYPS support. Vibrating sample magnetometry (VSM) analysis of CuFe
O
/HYPS showed paramagnetic behavior with a saturated magnetization value of 7.65 emu/g. DRS UV-vis analysis revealed the functionalization of cisplatin in tetrahedral and octahedral coordination in the CuFe
O
/HYPS composite. Compared to other supports such as mesocellular foam and silicalite, the release of cisplatin using the dialysis membrane technique was found to be superior when CuFe
O
/HYPS was applied as the support. An in vitro experiment was conducted to determine the potential of CuFe
O
/HYPS as an anticancer agent against the human breast cancer cell line MCF-7. The results show that the nanoparticle formulation can effectively target cancerous cells and could be an effective tumor imaging guide and drug delivery system. |
doi_str_mv | 10.3762/bjnano.10.214 |
format | Article |
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O
was impregnated into a matrix of monodispersed spherical hydrophilic silica (HYPS) nanoparticles through a simple dry impregnation technique. The chemotherapy drug cisplatin was loaded through electrostatic equilibrium adsorption over 24 h in normal saline solution. The presence of cubic spinel CuFe
O
on HYPS was confirmed through powder X-ray diffraction (PXRD), Fourier transform infrared spectroscopy (FTIR) and diffuse reflectance UV-vis spectroscopy (DR UV-vis) analysis. The HYPS particles showed a surface area of 170 m
/g, pore size of 8.3 nm and pore volume of 0.35 cm
/g. The cisplatin/CuFe
O
/HYPS nanoformulation showed the accumulation of copper ferrite nanoparticles on the surface and in the pores of HYPS with a surface area of 45 m
/g, pore size of 16 nm and pore volume of 0.18 cm
/g. Transmission electron microscopy (TEM) and energy dispersive X-ray (EDX) mapping analysis showed the presence of homogeneous silica particles with nanoclusters of copper ferrite distributed on the HYPS support. Vibrating sample magnetometry (VSM) analysis of CuFe
O
/HYPS showed paramagnetic behavior with a saturated magnetization value of 7.65 emu/g. DRS UV-vis analysis revealed the functionalization of cisplatin in tetrahedral and octahedral coordination in the CuFe
O
/HYPS composite. Compared to other supports such as mesocellular foam and silicalite, the release of cisplatin using the dialysis membrane technique was found to be superior when CuFe
O
/HYPS was applied as the support. An in vitro experiment was conducted to determine the potential of CuFe
O
/HYPS as an anticancer agent against the human breast cancer cell line MCF-7. The results show that the nanoparticle formulation can effectively target cancerous cells and could be an effective tumor imaging guide and drug delivery system.</description><identifier>ISSN: 2190-4286</identifier><identifier>EISSN: 2190-4286</identifier><identifier>DOI: 10.3762/bjnano.10.214</identifier><identifier>PMID: 31807407</identifier><language>eng</language><publisher>Germany</publisher><ispartof>Beilstein journal of nanotechnology, 2019-11, Vol.10, p.2217-2228</ispartof><rights>Copyright © 2019, Jermy et al.; licensee Beilstein-Institut.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c1057-68c22524eecf439ff04c0d25a7da134d94bd238059d090d1edbce3423fc4ecc13</citedby><cites>FETCH-LOGICAL-c1057-68c22524eecf439ff04c0d25a7da134d94bd238059d090d1edbce3423fc4ecc13</cites><orcidid>0000-0003-0963-5136 ; 0000-0002-8698-2820 ; 0000-0001-5678-5298</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,864,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31807407$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jermy, B Rabindran</creatorcontrib><creatorcontrib>Ravinayagam, Vijaya</creatorcontrib><creatorcontrib>Alamoudi, Widyan A</creatorcontrib><creatorcontrib>Almohazey, Dana</creatorcontrib><creatorcontrib>Dafalla, Hatim</creatorcontrib><creatorcontrib>Hussain Allehaibi, Lina</creatorcontrib><creatorcontrib>Baykal, Abdulhadi</creatorcontrib><creatorcontrib>Toprak, Muhammet S</creatorcontrib><creatorcontrib>Somanathan, Thirunavukkarasu</creatorcontrib><title>Targeted therapeutic effect against the breast cancer cell line MCF-7 with a CuFe 2 O 4 /silica/cisplatin nanocomposite formulation</title><title>Beilstein journal of nanotechnology</title><addtitle>Beilstein J Nanotechnol</addtitle><description>The combination of magnetic nanoparticles with a porous silica is a composite that has attracted significant attention for potential multifunctional theranostic applications. In this study, 30 wt % CuFe
O
was impregnated into a matrix of monodispersed spherical hydrophilic silica (HYPS) nanoparticles through a simple dry impregnation technique. The chemotherapy drug cisplatin was loaded through electrostatic equilibrium adsorption over 24 h in normal saline solution. The presence of cubic spinel CuFe
O
on HYPS was confirmed through powder X-ray diffraction (PXRD), Fourier transform infrared spectroscopy (FTIR) and diffuse reflectance UV-vis spectroscopy (DR UV-vis) analysis. The HYPS particles showed a surface area of 170 m
/g, pore size of 8.3 nm and pore volume of 0.35 cm
/g. The cisplatin/CuFe
O
/HYPS nanoformulation showed the accumulation of copper ferrite nanoparticles on the surface and in the pores of HYPS with a surface area of 45 m
/g, pore size of 16 nm and pore volume of 0.18 cm
/g. Transmission electron microscopy (TEM) and energy dispersive X-ray (EDX) mapping analysis showed the presence of homogeneous silica particles with nanoclusters of copper ferrite distributed on the HYPS support. Vibrating sample magnetometry (VSM) analysis of CuFe
O
/HYPS showed paramagnetic behavior with a saturated magnetization value of 7.65 emu/g. DRS UV-vis analysis revealed the functionalization of cisplatin in tetrahedral and octahedral coordination in the CuFe
O
/HYPS composite. Compared to other supports such as mesocellular foam and silicalite, the release of cisplatin using the dialysis membrane technique was found to be superior when CuFe
O
/HYPS was applied as the support. An in vitro experiment was conducted to determine the potential of CuFe
O
/HYPS as an anticancer agent against the human breast cancer cell line MCF-7. The results show that the nanoparticle formulation can effectively target cancerous cells and could be an effective tumor imaging guide and drug delivery system.</description><issn>2190-4286</issn><issn>2190-4286</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNpNkM1Lw0AQxRdRbKk9epX9B9LuV5rkKMGqUOmlnsNmdrbdki92E8Sz_7gJVXEu8x7vMQw_Qu45W8lkI9bludFNuxqt4OqKzAXPWKREurn-p2dkGcKZjaOYSLP0lswkT1miWDInXwftj9ijof0Jve5w6B1QtBahp_qoXRP6KaKlRz1K0A2gp4BVRSvXIH3Lt1FCP1x_oprmwxapoHuq6Dq4yoFegwtdpXvX0OlVaOuuDa5HaltfD1PQNnfkxuoq4PJnL8j79umQv0S7_fNr_riLgLM4iTYpCBELhQhWycxapoAZEevEaC6VyVRphExZnBmWMcPRlIBSCWlBIQCXCxJd7oJvQ_Boi867WvvPgrNi4llceE525Dn2Hy79bihrNH_tX3ryGxcgctU</recordid><startdate>20191112</startdate><enddate>20191112</enddate><creator>Jermy, B Rabindran</creator><creator>Ravinayagam, Vijaya</creator><creator>Alamoudi, Widyan A</creator><creator>Almohazey, Dana</creator><creator>Dafalla, Hatim</creator><creator>Hussain Allehaibi, Lina</creator><creator>Baykal, Abdulhadi</creator><creator>Toprak, Muhammet S</creator><creator>Somanathan, Thirunavukkarasu</creator><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0003-0963-5136</orcidid><orcidid>https://orcid.org/0000-0002-8698-2820</orcidid><orcidid>https://orcid.org/0000-0001-5678-5298</orcidid></search><sort><creationdate>20191112</creationdate><title>Targeted therapeutic effect against the breast cancer cell line MCF-7 with a CuFe 2 O 4 /silica/cisplatin nanocomposite formulation</title><author>Jermy, B Rabindran ; Ravinayagam, Vijaya ; Alamoudi, Widyan A ; Almohazey, Dana ; Dafalla, Hatim ; Hussain Allehaibi, Lina ; Baykal, Abdulhadi ; Toprak, Muhammet S ; Somanathan, Thirunavukkarasu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1057-68c22524eecf439ff04c0d25a7da134d94bd238059d090d1edbce3423fc4ecc13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jermy, B Rabindran</creatorcontrib><creatorcontrib>Ravinayagam, Vijaya</creatorcontrib><creatorcontrib>Alamoudi, Widyan A</creatorcontrib><creatorcontrib>Almohazey, Dana</creatorcontrib><creatorcontrib>Dafalla, Hatim</creatorcontrib><creatorcontrib>Hussain Allehaibi, Lina</creatorcontrib><creatorcontrib>Baykal, Abdulhadi</creatorcontrib><creatorcontrib>Toprak, Muhammet S</creatorcontrib><creatorcontrib>Somanathan, Thirunavukkarasu</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Beilstein journal of nanotechnology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jermy, B Rabindran</au><au>Ravinayagam, Vijaya</au><au>Alamoudi, Widyan A</au><au>Almohazey, Dana</au><au>Dafalla, Hatim</au><au>Hussain Allehaibi, Lina</au><au>Baykal, Abdulhadi</au><au>Toprak, Muhammet S</au><au>Somanathan, Thirunavukkarasu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Targeted therapeutic effect against the breast cancer cell line MCF-7 with a CuFe 2 O 4 /silica/cisplatin nanocomposite formulation</atitle><jtitle>Beilstein journal of nanotechnology</jtitle><addtitle>Beilstein J Nanotechnol</addtitle><date>2019-11-12</date><risdate>2019</risdate><volume>10</volume><spage>2217</spage><epage>2228</epage><pages>2217-2228</pages><issn>2190-4286</issn><eissn>2190-4286</eissn><abstract>The combination of magnetic nanoparticles with a porous silica is a composite that has attracted significant attention for potential multifunctional theranostic applications. In this study, 30 wt % CuFe
O
was impregnated into a matrix of monodispersed spherical hydrophilic silica (HYPS) nanoparticles through a simple dry impregnation technique. The chemotherapy drug cisplatin was loaded through electrostatic equilibrium adsorption over 24 h in normal saline solution. The presence of cubic spinel CuFe
O
on HYPS was confirmed through powder X-ray diffraction (PXRD), Fourier transform infrared spectroscopy (FTIR) and diffuse reflectance UV-vis spectroscopy (DR UV-vis) analysis. The HYPS particles showed a surface area of 170 m
/g, pore size of 8.3 nm and pore volume of 0.35 cm
/g. The cisplatin/CuFe
O
/HYPS nanoformulation showed the accumulation of copper ferrite nanoparticles on the surface and in the pores of HYPS with a surface area of 45 m
/g, pore size of 16 nm and pore volume of 0.18 cm
/g. Transmission electron microscopy (TEM) and energy dispersive X-ray (EDX) mapping analysis showed the presence of homogeneous silica particles with nanoclusters of copper ferrite distributed on the HYPS support. Vibrating sample magnetometry (VSM) analysis of CuFe
O
/HYPS showed paramagnetic behavior with a saturated magnetization value of 7.65 emu/g. DRS UV-vis analysis revealed the functionalization of cisplatin in tetrahedral and octahedral coordination in the CuFe
O
/HYPS composite. Compared to other supports such as mesocellular foam and silicalite, the release of cisplatin using the dialysis membrane technique was found to be superior when CuFe
O
/HYPS was applied as the support. An in vitro experiment was conducted to determine the potential of CuFe
O
/HYPS as an anticancer agent against the human breast cancer cell line MCF-7. The results show that the nanoparticle formulation can effectively target cancerous cells and could be an effective tumor imaging guide and drug delivery system.</abstract><cop>Germany</cop><pmid>31807407</pmid><doi>10.3762/bjnano.10.214</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0003-0963-5136</orcidid><orcidid>https://orcid.org/0000-0002-8698-2820</orcidid><orcidid>https://orcid.org/0000-0001-5678-5298</orcidid></addata></record> |
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title | Targeted therapeutic effect against the breast cancer cell line MCF-7 with a CuFe 2 O 4 /silica/cisplatin nanocomposite formulation |
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