2014
DOI: 10.1016/j.biomaterials.2014.02.011
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Magnetic and fluorescent graphene for dual modal imaging and single light induced photothermal and photodynamic therapy of cancer cells

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Cited by 169 publications
(134 citation statements)
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“…This phenomenon illustrates the inability of the heat generated from pure water under irradiation to cause cancer cell death and further confi rms the low cytotoxicity and good biocompatibility of C-dots. However, upon 635 nm laser irradiation (0.1 W cm −2 , 10 min), parts of the cells are destroyed after incubation with 200 µg mL −1 C-dots ( Figure 5 g) because of the ease with which 1 O 2 is produced and the inability to generate heat under such low laser power doses, [ 30 ] as previously discussed. Thus, PDT is predominant at low laser power doses.…”
Section: In Vitro Imaging and Pdt/pttmentioning
confidence: 90%
See 1 more Smart Citation
“…This phenomenon illustrates the inability of the heat generated from pure water under irradiation to cause cancer cell death and further confi rms the low cytotoxicity and good biocompatibility of C-dots. However, upon 635 nm laser irradiation (0.1 W cm −2 , 10 min), parts of the cells are destroyed after incubation with 200 µg mL −1 C-dots ( Figure 5 g) because of the ease with which 1 O 2 is produced and the inability to generate heat under such low laser power doses, [ 30 ] as previously discussed. Thus, PDT is predominant at low laser power doses.…”
Section: In Vitro Imaging and Pdt/pttmentioning
confidence: 90%
“…This fi nding is attributed to the fact that at high power doses, C-dots can simultaneously generate 1 O 2 and produce heat to efficiently kill cells by simultaneous PDT and PTT using a single red laser. [ 30 ] We further quantitatively evaluated the cytotoxicity and bimodal PDT/PTT effi cacy of C-dots using MTT assay. As presented in Figure 5 i, 200 µg mL −1 of C-dots does not have any effect on cancer cell survival without laser irradiation.…”
Section: In Vitro Imaging and Pdt/pttmentioning
confidence: 99%
“…26 A noncovalent method was used to immobilize photosensitizers onto graphene via π-π stacking, which caused a significant reduction in the fluorescence and ROS generation as a result of a π-π stacking interaction with graphene. 21,22,26,27 To overcome the aforementioned obstacles, we developed a novel ovarian cancer-targeted nanomedicine platform that preserves fluorescence imaging and ROS-generating capabilities of the photosensitizer immobilized on the graphene surface. In our design, graphene nanosheets were chemically conjugated with polypropylenimine generation 4 (PPIG4) dendrimer loaded with silicon Pc derivative to produce a LOGr-Pc-PPIG4 complex ( Figure 1).…”
mentioning
confidence: 99%
“…12,13,42 Despite a strong absorption signal in the NIR optical window, previously developed nanoplatforms based on hydrophobic interactions and π-π stacking between photosensitizers and graphene oxides have been characterized by drastic fluorescence quenching of the photosensitizer and a significant decrease in ROS generation. 24,26,43 This is related to …”
mentioning
confidence: 99%
“…164 In another study, Gollavelli et al developed SiNc 4 photosensitizer loaded magnetic°uorescent graphene and demonstrated bimodal°u orescence/MRI imaging guided combined photothermal-photodynamic therapy of HeLa cells in vitro. 165 …”
Section: Multimodal Imaging-guided Phototherapymentioning
confidence: 99%