Co-delivery of doxorubicin and small interfering RNA with genipin-cross-linked iron (III) oxide-polyetherimide nanoparticles for combined cancer therapy
To solve the problem of tumor multidrug resistance in cancer therapy, a new drug delivery system of genipin-cross-linked iron (III) oxide/polyetherimide nanoparticles was used to load doxorubicin and small interfering RNA for combined cancer therapy. The results showed that the drug loading and enca...
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Veröffentlicht in: | Nanomaterials and nanotechnology 2017-01, Vol.7, p.184798041770409 |
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creator | Long, Ruimin Liu, Yuangang Wu, Shenjian Wang, Shibin Wang, Pei |
description | To solve the problem of tumor multidrug resistance in cancer therapy, a new drug delivery system of genipin-cross-linked iron (III) oxide/polyetherimide nanoparticles was used to load doxorubicin and small interfering RNA for combined cancer therapy. The results showed that the drug loading and encapsulation efficiency of doxorubicin could reach 45.39% and 52.18%, respectively. Doxorubicin released from iron (III) oxide-polyetherimide-doxorubicin is about 40% in the first day and 95% in 14 days. When loading doxorubicin and small interfering RNA, small interfering RNA could be absorbed completely. Besides, small interfering RNA could strengthen the anticancer effect when iron (III) oxide-polyetherimide-doxorubicin/small interfering RNA was used for in vitro HeLa cell combined treatment, and the effect of combination group was better than that of the group with doxorubicin alone. In addition, the toxicity of iron (III) oxide-polyetherimide was low when examined by the Alamar Blue assay. Therefore, our results reveal that this new system has potential applications in the future drug combination therapy, especially in the combined targeting drug delivery field. |
doi_str_mv | 10.1177/1847980417704094 |
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The results showed that the drug loading and encapsulation efficiency of doxorubicin could reach 45.39% and 52.18%, respectively. Doxorubicin released from iron (III) oxide-polyetherimide-doxorubicin is about 40% in the first day and 95% in 14 days. When loading doxorubicin and small interfering RNA, small interfering RNA could be absorbed completely. Besides, small interfering RNA could strengthen the anticancer effect when iron (III) oxide-polyetherimide-doxorubicin/small interfering RNA was used for in vitro HeLa cell combined treatment, and the effect of combination group was better than that of the group with doxorubicin alone. In addition, the toxicity of iron (III) oxide-polyetherimide was low when examined by the Alamar Blue assay. Therefore, our results reveal that this new system has potential applications in the future drug combination therapy, especially in the combined targeting drug delivery field.</description><identifier>ISSN: 1847-9804</identifier><identifier>EISSN: 1847-9804</identifier><identifier>DOI: 10.1177/1847980417704094</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><subject>Anticancer properties ; Cancer ; Cancer therapies ; Crosslinking ; Doxorubicin ; Drug delivery systems ; Genipin ; Iron ; Nanoparticles ; Polyetherimides ; Ribonucleic acid ; RNA ; Therapy ; Toxicity</subject><ispartof>Nanomaterials and nanotechnology, 2017-01, Vol.7, p.184798041770409</ispartof><rights>The Author(s) 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c234t-55ac897582bd41c4e32ebf0e42561f1fcd370ca3faba7a76ec3c2a81ef0ba4ef3</cites></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></links><search><creatorcontrib>Long, Ruimin</creatorcontrib><creatorcontrib>Liu, Yuangang</creatorcontrib><creatorcontrib>Wu, Shenjian</creatorcontrib><creatorcontrib>Wang, Shibin</creatorcontrib><creatorcontrib>Wang, Pei</creatorcontrib><title>Co-delivery of doxorubicin and small interfering RNA with genipin-cross-linked iron (III) oxide-polyetherimide nanoparticles for combined cancer therapy</title><title>Nanomaterials and nanotechnology</title><description>To solve the problem of tumor multidrug resistance in cancer therapy, a new drug delivery system of genipin-cross-linked iron (III) oxide/polyetherimide nanoparticles was used to load doxorubicin and small interfering RNA for combined cancer therapy. The results showed that the drug loading and encapsulation efficiency of doxorubicin could reach 45.39% and 52.18%, respectively. Doxorubicin released from iron (III) oxide-polyetherimide-doxorubicin is about 40% in the first day and 95% in 14 days. When loading doxorubicin and small interfering RNA, small interfering RNA could be absorbed completely. Besides, small interfering RNA could strengthen the anticancer effect when iron (III) oxide-polyetherimide-doxorubicin/small interfering RNA was used for in vitro HeLa cell combined treatment, and the effect of combination group was better than that of the group with doxorubicin alone. In addition, the toxicity of iron (III) oxide-polyetherimide was low when examined by the Alamar Blue assay. Therefore, our results reveal that this new system has potential applications in the future drug combination therapy, especially in the combined targeting drug delivery field.</description><subject>Anticancer properties</subject><subject>Cancer</subject><subject>Cancer therapies</subject><subject>Crosslinking</subject><subject>Doxorubicin</subject><subject>Drug delivery systems</subject><subject>Genipin</subject><subject>Iron</subject><subject>Nanoparticles</subject><subject>Polyetherimides</subject><subject>Ribonucleic acid</subject><subject>RNA</subject><subject>Therapy</subject><subject>Toxicity</subject><issn>1847-9804</issn><issn>1847-9804</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>AFRWT</sourceid><recordid>eNp1UU1LxDAQLaLgsu7dY8CLHqJJmm7b47L4UVgURM8lTSe7WbtJTbq6_Sf-XFNXUATnMm-G997wmCg6peSS0jS9ohlP84zwgAknOT-IRsMKD7vDX_g4mni_JqFyTmOWjqKPucU1NPoNXI-sQrXdWbettNQGCVMjvxFNg7TpwClw2izR4_0MvetuhZZgdKsNls56jxttXqBG2lmDzouiuEB2p2vArW166FZBuwkjMsLYVrhOywY8UtYhaTeVNkEqhZHg0MAVbX8SHSnReJh893H0fHP9NL_Di4fbYj5bYMli3uEkETLL0yRjVc2p5BAzqBQBzpIpVVTJOk6JFLESlUhFOgUZSyYyCopUgoOKx9HZ3rd19nULvivXdutMOFkympGMTRmNA4vsWV9hHaiyDYGE60tKyuEF5d8XBAneS7xYwo_pv_xPY3iJSw</recordid><startdate>20170101</startdate><enddate>20170101</enddate><creator>Long, Ruimin</creator><creator>Liu, Yuangang</creator><creator>Wu, Shenjian</creator><creator>Wang, Shibin</creator><creator>Wang, Pei</creator><general>SAGE Publications</general><general>Hindawi Limited</general><scope>AFRWT</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7U5</scope><scope>8FD</scope><scope>L7M</scope></search><sort><creationdate>20170101</creationdate><title>Co-delivery of doxorubicin and small interfering RNA with genipin-cross-linked iron (III) oxide-polyetherimide nanoparticles for combined cancer therapy</title><author>Long, Ruimin ; Liu, Yuangang ; Wu, Shenjian ; Wang, Shibin ; Wang, Pei</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c234t-55ac897582bd41c4e32ebf0e42561f1fcd370ca3faba7a76ec3c2a81ef0ba4ef3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Anticancer properties</topic><topic>Cancer</topic><topic>Cancer therapies</topic><topic>Crosslinking</topic><topic>Doxorubicin</topic><topic>Drug delivery systems</topic><topic>Genipin</topic><topic>Iron</topic><topic>Nanoparticles</topic><topic>Polyetherimides</topic><topic>Ribonucleic acid</topic><topic>RNA</topic><topic>Therapy</topic><topic>Toxicity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Long, Ruimin</creatorcontrib><creatorcontrib>Liu, Yuangang</creatorcontrib><creatorcontrib>Wu, Shenjian</creatorcontrib><creatorcontrib>Wang, Shibin</creatorcontrib><creatorcontrib>Wang, Pei</creatorcontrib><collection>Sage Journals GOLD Open Access 2024</collection><collection>CrossRef</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Nanomaterials and nanotechnology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Long, Ruimin</au><au>Liu, Yuangang</au><au>Wu, Shenjian</au><au>Wang, Shibin</au><au>Wang, Pei</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Co-delivery of doxorubicin and small interfering RNA with genipin-cross-linked iron (III) oxide-polyetherimide nanoparticles for combined cancer therapy</atitle><jtitle>Nanomaterials and nanotechnology</jtitle><date>2017-01-01</date><risdate>2017</risdate><volume>7</volume><spage>184798041770409</spage><pages>184798041770409-</pages><issn>1847-9804</issn><eissn>1847-9804</eissn><abstract>To solve the problem of tumor multidrug resistance in cancer therapy, a new drug delivery system of genipin-cross-linked iron (III) oxide/polyetherimide nanoparticles was used to load doxorubicin and small interfering RNA for combined cancer therapy. The results showed that the drug loading and encapsulation efficiency of doxorubicin could reach 45.39% and 52.18%, respectively. Doxorubicin released from iron (III) oxide-polyetherimide-doxorubicin is about 40% in the first day and 95% in 14 days. When loading doxorubicin and small interfering RNA, small interfering RNA could be absorbed completely. Besides, small interfering RNA could strengthen the anticancer effect when iron (III) oxide-polyetherimide-doxorubicin/small interfering RNA was used for in vitro HeLa cell combined treatment, and the effect of combination group was better than that of the group with doxorubicin alone. In addition, the toxicity of iron (III) oxide-polyetherimide was low when examined by the Alamar Blue assay. Therefore, our results reveal that this new system has potential applications in the future drug combination therapy, especially in the combined targeting drug delivery field.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><doi>10.1177/1847980417704094</doi><oa>free_for_read</oa></addata></record> |
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subjects | Anticancer properties Cancer Cancer therapies Crosslinking Doxorubicin Drug delivery systems Genipin Iron Nanoparticles Polyetherimides Ribonucleic acid RNA Therapy Toxicity |
title | Co-delivery of doxorubicin and small interfering RNA with genipin-cross-linked iron (III) oxide-polyetherimide nanoparticles for combined cancer therapy |
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