2021
DOI: 10.1016/j.msec.2020.111809
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Glucosamine-conjugated graphene quantum dots as versatile and pH-sensitive nanocarriers for enhanced delivery of curcumin targeting to breast cancer

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Cited by 36 publications
(15 citation statements)
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“…The described system showed high cellular uptake, high in vitro and in vivo efficacy, and low toxicity. Glucosamine-conjugated GRQDs, showing a size of 20–30 nm and <10 layers, releasing after 150 h 37% and 17% of encapsulated CUR at pH 5.5 and pH 7.4, respectively, showed higher cellular internalization via glucosamine-receptor-mediated endocytosis in breast cancer cells as well as pronouncedly higher cytotoxicity against MCF-7 cells, compared to CUR/GRQDs [ 104 ]. Tryptophan-functionalized GRQDs were also characterized with high CUR-loading capacity and pH-sensitivity [ 105 ].…”
Section: Gbns As Drugs and Nanocarriersmentioning
confidence: 99%
“…The described system showed high cellular uptake, high in vitro and in vivo efficacy, and low toxicity. Glucosamine-conjugated GRQDs, showing a size of 20–30 nm and <10 layers, releasing after 150 h 37% and 17% of encapsulated CUR at pH 5.5 and pH 7.4, respectively, showed higher cellular internalization via glucosamine-receptor-mediated endocytosis in breast cancer cells as well as pronouncedly higher cytotoxicity against MCF-7 cells, compared to CUR/GRQDs [ 104 ]. Tryptophan-functionalized GRQDs were also characterized with high CUR-loading capacity and pH-sensitivity [ 105 ].…”
Section: Gbns As Drugs and Nanocarriersmentioning
confidence: 99%
“…Complexes that include photoluminescent graphene quantum dots with glucosamine as a targeting agent, and with curcumin as an anticancer agent, have been proven to inhibit cells of the MCF-7 breast cancer line, a result that sounds promising due to the observed behavior pH-sensitive, sustained release for nano-assembly (25). Graphitic carbon nitride (g-C3N4) Quantum Dots synthesized through the usual calcination method served as nanoplatforms for dual two-photon excited photodynamic therapy (TPE-PDT) and two-photon imaging (TPI) (26).…”
Section: Graphene In Breast Cancermentioning
confidence: 99%
“…Glucose and GlcN are delivered to cells via various glucose transporters (GLUTs) and sodium glucose transporters (SGLTs) expressed on cell membranes [9,16], many of which are overexpressed on tumor cells to facilitate glucose and GlcN delivery [17]. Owing to the aforementioned higher GlcN demand by tumor cells than by normal cells (GlcN effects) and the -NH 2 group of GlcN, which allows easy conjugation with the -COOH group of functional agents via an amide bond (-OH group of glucose is not easy for conjugation), GlcN has been widely applied as a conjugation ligand to increase delivery amounts of antitumor drugs [18][19][20][21], tumor imaging agents [21][22][23], and tumor therapeutic agents [24]. GlcN had been conjugated with various materials for drug delivery to tumor, tumor imaging, and tumor therapy.…”
Section: Introductionmentioning
confidence: 99%
“…GlcN had been conjugated with various materials for drug delivery to tumor, tumor imaging, and tumor therapy. These included poly(amidoamine) dendrimers to deliver camptothecin antitumor drug to human lung tumor (A549) cells in vitro and in vivo [18], graphene quantum dots to deliver curcumin antitumor drug to human breast tumor (MCF-7) cells in vitro [19], niosomal formulation to deliver doxorubicin antitumor drug to skin melanoma tumor (B6F10) cells in vitro [20], InP/ZnS quantum dots to deliver doxorubicin to human lung epithelial tumor (A549) cells and human ovarian tumor (OVCAR-3) cells in vitro and to image tumor cells [21], near infrared fluorescent probes for breast [22] and prostate [23] tumor imaging in vitro and in vivo, and multifunctional doxorubicin loaded gadolinium/cobalt@iron oxide-dendrimer-nanoseeds for chemo-magneto hyperthermia treatment of human prostate tumor (PC3) cells in vitro [24].…”
Section: Introductionmentioning
confidence: 99%