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dc.contributor.authorOcsoy, Ismail
dc.contributor.authorIsiklan, Nuran
dc.contributor.authorCansiz, Sena
dc.contributor.authorOzdemir, Nalan
dc.contributor.authorTan, Weihong
dc.date.accessioned2020-06-25T18:22:28Z
dc.date.available2020-06-25T18:22:28Z
dc.date.issued2016
dc.identifier.citationOcsoy, I., Isiklan, N., Cansiz, S., Özdemir, N., & Tan, W. (2016). ICG-conjugated Magnetic Graphene Oxide for Dual Photothermal and Photodynamic Therapy. RSC advances, 6(36), 30285–30292.en_US
dc.identifier.issn2046-2069
dc.identifier.urihttps://doi.org/10.1039/c6ra06798k
dc.identifier.urihttps://hdl.handle.net/20.500.12587/6754
dc.descriptionTan, Weihong/0000-0002-8066-1524;en_US
dc.descriptionWOS: 000373061600049en_US
dc.descriptionPubMed: 27774142en_US
dc.description.abstractAptamer-functionalized magnetic graphene oxide conjugates loaded with indocyanine green (ICG) dye, or Apt@ICG@mGO, have been successfully developed for dual-targeted photothermal and photodynamic therapy. In general, a drug or its carrier or their dosage can be important issues in terms of toxicity. However, in this system, each component used is quite safe, biocompatible and clean. For instance, ICG, a Food and Drug Administration (FDA) approved near-infrared (NIR) dye, serves as both a photothermal and photodynamic agent. It is immobilized on the surface of mGO via a physical interaction called "pi-pi stacking". The mGO, as a most biocompatible member of the carbo family, is selected for use as a platform for aptamer and ICG dye conjugation, as well as a photothermal agent. The light in the near-infrared region (NIR) was chosen as a harmless light source for activating the agents for photothermal therapy (PTT) and photodynamic therapy (PDT). The magnetic properties of mGO are also used for separation of Apt@ICG@mGO conjugates from the reaction medium. Aptamer sgc8 acts as a targeting ligand to selectively and specifically bind to a protein on the membrane of cancer cell line CCRF-CEM. After the aptamer-functionalized ICG@mGO conjugates are incubated with target CEM cells at 37 degrees C for 2 hours, they are bound to cells or they may be internalized into the cell via endocytosis. More significantly, we demonstrated that the Apt@ICG@mGO conjugates produce heat for photothermal therapy (PTT) and singlet oxygen for photodynamic therapy (PDT) upon NIR laser irradiation at 808 nm. Thus, remarkably efficient cancer cell destructions with similar to 41% and similar to 60% and similar to 82% cell killing using 10, 50 and 100 ppm Apt@ICG@mGO, respectively are achieved in 5 min light exposure.en_US
dc.description.sponsorshipNational Institutes of HealthUnited States Department of Health & Human ServicesNational Institutes of Health (NIH) - USA [GM079359, CA133086]en_US
dc.description.sponsorshipThis work is supported by grants awarded by the National Institutes of Health (GM079359 and CA133086). The authors sincerely thank Dr Kathryn Williams for assistance with manuscript revision and John W. Munson in the Center for Environment and Human Toxicology (CEHT) at the University of Florida for laser support.en_US
dc.language.isoengen_US
dc.publisherRoyal Soc Chemistryen_US
dc.relation.isversionof10.1039/c6ra06798ken_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.titleICG-Conjugated magnetic graphene oxide for dual photothermal and photodynamic therapyen_US
dc.typearticleen_US
dc.contributor.departmentKırıkkale Üniversitesien_US
dc.identifier.volume6en_US
dc.identifier.issue36en_US
dc.identifier.startpage30285en_US
dc.identifier.endpage30292en_US
dc.relation.journalRsc Advancesen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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