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Merging High Doxorubicin Loading with Pronounced Magnetic Response and Bio-repellent Properties in Hybrid Drug Nanocarriers
Hybrid magnetic drug nanocarriers are prepared via a self‐assembly process of poly(methacrylic acid)‐graft‐poly(ethyleneglycol methacrylate) (p(MAA‐g‐EGMA)) on growing iron oxide nanocrystallites. The nanocarriers successfully merge together bio‐repellent properties, pronounced magnetic response, an...
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Published in: | Small (Weinheim an der Bergstrasse, Germany) Germany), 2012-08, Vol.8 (15), p.2381-2393 |
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creator | Bakandritsos, Aristides Papagiannopoulos, Aristeidis Anagnostou, Eleni N. Avgoustakis, Konstantinos Zboril, Radek Pispas, Stergios Tucek, Jiri Ryukhtin, Vasyl Bouropoulos, Nikolaos Kolokithas-Ntoukas, Argiris Steriotis, Theodore A. Keiderling, Uwe Winnefeld, Frank |
description | Hybrid magnetic drug nanocarriers are prepared via a self‐assembly process of poly(methacrylic acid)‐graft‐poly(ethyleneglycol methacrylate) (p(MAA‐g‐EGMA)) on growing iron oxide nanocrystallites. The nanocarriers successfully merge together bio‐repellent properties, pronounced magnetic response, and high loading capacity for the potent anticancer drug doxorubicin (adriamicin), in a manner not observed before in such hybrid colloids. High magnetic responses are accomplished by engineering the size of the magnetic nanocrystallites (∼13.5 nm) following an aqueous single‐ferrous precursor route, and through adjustment of the number of cores in each colloidal assembly. Complementing conventional magnetometry, the magnetic response of the nanocarriers is evaluated by magnetophoretic experiments providing insight into their internal organization and on their response to magnetic manipulation. The structural organization of the graft‐copolymer, locked on the surface of the nanocrystallites, is further probed by small‐angle neutron scattering on single‐core colloids. Analysis showed that the MAA segments selectively populate the area around the magnetic nanocrystallites, while the poly(ethylene glycol)‐grafted chains are arranged as protrusions, pointing towards the aqueous environment. These nanocarriers are screened at various pHs and in highly salted media by light scattering and electrokinetic measurements. According to the results, their stability is dramatically enhanced, as compared to uncoated nanocrystallites, owing to the presence of the external protective PEG canopy. The nanocarriers are also endowed with bio‐repellent properties, as evidenced by stability assays using human blood plasma as the medium.
Hybrid drug nanocarriers simultaneously exhibit bio‐repellent properties, pronounced magnetic response, high loading capacity of the potent anticancer drug doxorubicin, in a manner that has not been attained before. The nanocarriers are based on a magnetic core and a two‐layer bi‐functional polymeric corona constituted from a polycarboxylate backbone and poly(ethylene glycol) branches. |
doi_str_mv | 10.1002/smll.201102525 |
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Hybrid drug nanocarriers simultaneously exhibit bio‐repellent properties, pronounced magnetic response, high loading capacity of the potent anticancer drug doxorubicin, in a manner that has not been attained before. The nanocarriers are based on a magnetic core and a two‐layer bi‐functional polymeric corona constituted from a polycarboxylate backbone and poly(ethylene glycol) branches.</description><identifier>ISSN: 1613-6810</identifier><identifier>EISSN: 1613-6829</identifier><identifier>DOI: 10.1002/smll.201102525</identifier><identifier>PMID: 22549909</identifier><language>eng</language><publisher>Weinheim: WILEY-VCH Verlag</publisher><subject>bio-repellent materials ; Doxorubicin - administration & dosage ; Doxorubicin - chemistry ; Drug Carriers - chemistry ; drug delivery ; hybrid materials ; magnetic targeting ; Magnetics ; Microscopy, Electron, Transmission ; nanocarriers ; Nanoparticles - chemistry ; Polyethylene Glycols - chemistry ; Thermogravimetry</subject><ispartof>Small (Weinheim an der Bergstrasse, Germany), 2012-08, Vol.8 (15), p.2381-2393</ispartof><rights>Copyright © 2012 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><rights>Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3835-cb1b66853aacb1ce430e39c3e361c52a9d64baab98a5ff77805f7eb317e215fe3</citedby><cites>FETCH-LOGICAL-c3835-cb1b66853aacb1ce430e39c3e361c52a9d64baab98a5ff77805f7eb317e215fe3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22549909$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bakandritsos, Aristides</creatorcontrib><creatorcontrib>Papagiannopoulos, Aristeidis</creatorcontrib><creatorcontrib>Anagnostou, Eleni N.</creatorcontrib><creatorcontrib>Avgoustakis, Konstantinos</creatorcontrib><creatorcontrib>Zboril, Radek</creatorcontrib><creatorcontrib>Pispas, Stergios</creatorcontrib><creatorcontrib>Tucek, Jiri</creatorcontrib><creatorcontrib>Ryukhtin, Vasyl</creatorcontrib><creatorcontrib>Bouropoulos, Nikolaos</creatorcontrib><creatorcontrib>Kolokithas-Ntoukas, Argiris</creatorcontrib><creatorcontrib>Steriotis, Theodore A.</creatorcontrib><creatorcontrib>Keiderling, Uwe</creatorcontrib><creatorcontrib>Winnefeld, Frank</creatorcontrib><title>Merging High Doxorubicin Loading with Pronounced Magnetic Response and Bio-repellent Properties in Hybrid Drug Nanocarriers</title><title>Small (Weinheim an der Bergstrasse, Germany)</title><addtitle>Small</addtitle><description>Hybrid magnetic drug nanocarriers are prepared via a self‐assembly process of poly(methacrylic acid)‐graft‐poly(ethyleneglycol methacrylate) (p(MAA‐g‐EGMA)) on growing iron oxide nanocrystallites. The nanocarriers successfully merge together bio‐repellent properties, pronounced magnetic response, and high loading capacity for the potent anticancer drug doxorubicin (adriamicin), in a manner not observed before in such hybrid colloids. High magnetic responses are accomplished by engineering the size of the magnetic nanocrystallites (∼13.5 nm) following an aqueous single‐ferrous precursor route, and through adjustment of the number of cores in each colloidal assembly. Complementing conventional magnetometry, the magnetic response of the nanocarriers is evaluated by magnetophoretic experiments providing insight into their internal organization and on their response to magnetic manipulation. The structural organization of the graft‐copolymer, locked on the surface of the nanocrystallites, is further probed by small‐angle neutron scattering on single‐core colloids. Analysis showed that the MAA segments selectively populate the area around the magnetic nanocrystallites, while the poly(ethylene glycol)‐grafted chains are arranged as protrusions, pointing towards the aqueous environment. These nanocarriers are screened at various pHs and in highly salted media by light scattering and electrokinetic measurements. According to the results, their stability is dramatically enhanced, as compared to uncoated nanocrystallites, owing to the presence of the external protective PEG canopy. The nanocarriers are also endowed with bio‐repellent properties, as evidenced by stability assays using human blood plasma as the medium.
Hybrid drug nanocarriers simultaneously exhibit bio‐repellent properties, pronounced magnetic response, high loading capacity of the potent anticancer drug doxorubicin, in a manner that has not been attained before. The nanocarriers are based on a magnetic core and a two‐layer bi‐functional polymeric corona constituted from a polycarboxylate backbone and poly(ethylene glycol) branches.</description><subject>bio-repellent materials</subject><subject>Doxorubicin - administration & dosage</subject><subject>Doxorubicin - chemistry</subject><subject>Drug Carriers - chemistry</subject><subject>drug delivery</subject><subject>hybrid materials</subject><subject>magnetic targeting</subject><subject>Magnetics</subject><subject>Microscopy, Electron, Transmission</subject><subject>nanocarriers</subject><subject>Nanoparticles - chemistry</subject><subject>Polyethylene Glycols - chemistry</subject><subject>Thermogravimetry</subject><issn>1613-6810</issn><issn>1613-6829</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNqFkEtP3DAURq2qVXl1yxJ52U0GP8ZJvCwMMEgZnq2K2FiOcxNcMnawE8Gof74ZDR1119W90j3fp6uD0CElE0oIO47Ltp0wQilhgokPaJemlCdpzuTH7U7JDtqL8RchnLJp9hntMCamUhK5i34vIDTWNXhumyc8828-DKU11uHC62p9eLX9E74J3vnBGajwQjcOemvwHcTOuwhYuwqfWJ8E6KBtwfVrvIPQW4h4bJqvymArPAtDg6-080aHYCHEA_Sp1m2EL-9zH_04P_t-Ok-K64vL029FYnjORWJKWqZpLrjW42pgyglwaTjwlBrBtKzSaal1KXMt6jrLciLqDEpOM2BU1MD30ddNbxf8ywCxV0sbzfiqduCHqOjohaaMUTaikw1qgo8xQK26YJc6rEZIrYWrtXC1FT4Gjt67h3IJ1Rb_a3gE5AZ4tS2s_lOn7hdF8W95ssna2MPbNqvDs0ozngn18-pCSTa_ZbPHB8X5H1I3nlE</recordid><startdate>20120806</startdate><enddate>20120806</enddate><creator>Bakandritsos, Aristides</creator><creator>Papagiannopoulos, Aristeidis</creator><creator>Anagnostou, Eleni N.</creator><creator>Avgoustakis, Konstantinos</creator><creator>Zboril, Radek</creator><creator>Pispas, Stergios</creator><creator>Tucek, Jiri</creator><creator>Ryukhtin, Vasyl</creator><creator>Bouropoulos, Nikolaos</creator><creator>Kolokithas-Ntoukas, Argiris</creator><creator>Steriotis, Theodore A.</creator><creator>Keiderling, Uwe</creator><creator>Winnefeld, Frank</creator><general>WILEY-VCH Verlag</general><general>WILEY‐VCH Verlag</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20120806</creationdate><title>Merging High Doxorubicin Loading with Pronounced Magnetic Response and Bio-repellent Properties in Hybrid Drug Nanocarriers</title><author>Bakandritsos, Aristides ; Papagiannopoulos, Aristeidis ; Anagnostou, Eleni N. ; Avgoustakis, Konstantinos ; Zboril, Radek ; Pispas, Stergios ; Tucek, Jiri ; Ryukhtin, Vasyl ; Bouropoulos, Nikolaos ; Kolokithas-Ntoukas, Argiris ; Steriotis, Theodore A. ; Keiderling, Uwe ; Winnefeld, Frank</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3835-cb1b66853aacb1ce430e39c3e361c52a9d64baab98a5ff77805f7eb317e215fe3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>bio-repellent materials</topic><topic>Doxorubicin - administration & dosage</topic><topic>Doxorubicin - chemistry</topic><topic>Drug Carriers - chemistry</topic><topic>drug delivery</topic><topic>hybrid materials</topic><topic>magnetic targeting</topic><topic>Magnetics</topic><topic>Microscopy, Electron, Transmission</topic><topic>nanocarriers</topic><topic>Nanoparticles - chemistry</topic><topic>Polyethylene Glycols - chemistry</topic><topic>Thermogravimetry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bakandritsos, Aristides</creatorcontrib><creatorcontrib>Papagiannopoulos, Aristeidis</creatorcontrib><creatorcontrib>Anagnostou, Eleni N.</creatorcontrib><creatorcontrib>Avgoustakis, Konstantinos</creatorcontrib><creatorcontrib>Zboril, Radek</creatorcontrib><creatorcontrib>Pispas, Stergios</creatorcontrib><creatorcontrib>Tucek, Jiri</creatorcontrib><creatorcontrib>Ryukhtin, Vasyl</creatorcontrib><creatorcontrib>Bouropoulos, Nikolaos</creatorcontrib><creatorcontrib>Kolokithas-Ntoukas, Argiris</creatorcontrib><creatorcontrib>Steriotis, Theodore A.</creatorcontrib><creatorcontrib>Keiderling, Uwe</creatorcontrib><creatorcontrib>Winnefeld, Frank</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Small (Weinheim an der Bergstrasse, Germany)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bakandritsos, Aristides</au><au>Papagiannopoulos, Aristeidis</au><au>Anagnostou, Eleni N.</au><au>Avgoustakis, Konstantinos</au><au>Zboril, Radek</au><au>Pispas, Stergios</au><au>Tucek, Jiri</au><au>Ryukhtin, Vasyl</au><au>Bouropoulos, Nikolaos</au><au>Kolokithas-Ntoukas, Argiris</au><au>Steriotis, Theodore A.</au><au>Keiderling, Uwe</au><au>Winnefeld, Frank</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Merging High Doxorubicin Loading with Pronounced Magnetic Response and Bio-repellent Properties in Hybrid Drug Nanocarriers</atitle><jtitle>Small (Weinheim an der Bergstrasse, Germany)</jtitle><addtitle>Small</addtitle><date>2012-08-06</date><risdate>2012</risdate><volume>8</volume><issue>15</issue><spage>2381</spage><epage>2393</epage><pages>2381-2393</pages><issn>1613-6810</issn><eissn>1613-6829</eissn><abstract>Hybrid magnetic drug nanocarriers are prepared via a self‐assembly process of poly(methacrylic acid)‐graft‐poly(ethyleneglycol methacrylate) (p(MAA‐g‐EGMA)) on growing iron oxide nanocrystallites. The nanocarriers successfully merge together bio‐repellent properties, pronounced magnetic response, and high loading capacity for the potent anticancer drug doxorubicin (adriamicin), in a manner not observed before in such hybrid colloids. High magnetic responses are accomplished by engineering the size of the magnetic nanocrystallites (∼13.5 nm) following an aqueous single‐ferrous precursor route, and through adjustment of the number of cores in each colloidal assembly. Complementing conventional magnetometry, the magnetic response of the nanocarriers is evaluated by magnetophoretic experiments providing insight into their internal organization and on their response to magnetic manipulation. The structural organization of the graft‐copolymer, locked on the surface of the nanocrystallites, is further probed by small‐angle neutron scattering on single‐core colloids. Analysis showed that the MAA segments selectively populate the area around the magnetic nanocrystallites, while the poly(ethylene glycol)‐grafted chains are arranged as protrusions, pointing towards the aqueous environment. These nanocarriers are screened at various pHs and in highly salted media by light scattering and electrokinetic measurements. According to the results, their stability is dramatically enhanced, as compared to uncoated nanocrystallites, owing to the presence of the external protective PEG canopy. The nanocarriers are also endowed with bio‐repellent properties, as evidenced by stability assays using human blood plasma as the medium.
Hybrid drug nanocarriers simultaneously exhibit bio‐repellent properties, pronounced magnetic response, high loading capacity of the potent anticancer drug doxorubicin, in a manner that has not been attained before. The nanocarriers are based on a magnetic core and a two‐layer bi‐functional polymeric corona constituted from a polycarboxylate backbone and poly(ethylene glycol) branches.</abstract><cop>Weinheim</cop><pub>WILEY-VCH Verlag</pub><pmid>22549909</pmid><doi>10.1002/smll.201102525</doi><tpages>13</tpages></addata></record> |
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subjects | bio-repellent materials Doxorubicin - administration & dosage Doxorubicin - chemistry Drug Carriers - chemistry drug delivery hybrid materials magnetic targeting Magnetics Microscopy, Electron, Transmission nanocarriers Nanoparticles - chemistry Polyethylene Glycols - chemistry Thermogravimetry |
title | Merging High Doxorubicin Loading with Pronounced Magnetic Response and Bio-repellent Properties in Hybrid Drug Nanocarriers |
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