2019
DOI: 10.1016/j.msec.2019.03.011
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Development of biotin molecule targeted cancer cell drug delivery of doxorubicin loaded κ-carrageenan grafted graphene oxide nanocarrier

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Cited by 77 publications
(32 citation statements)
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“…This is also a good evidence that PEGylation occurred regioselectively at both GO surfaces.The functionalization of GO sheets with PEG-Fol chains was also established by means of AFM and SEM microscopies (Figure 5).Figure 5ashows a typical dimensional distribution analysis of GO-PEG-Fol, where the presence of GO islands with a thickness of about 3.5 nm and a diameter of about 40 ± 4 nm can be observed. The increase of the nano-flakes thickness of about 2.5 nm can be explained with a homogeneous functionalization of the GO surface with Fol-PEG-CC chains of 2.5 kDa, corroborating UV and FTIR data [5,42]. It might be noticed that the small size and the narrow size distribution observed are suitable for biomedical applications, especially as carrier for anticancer drugs, since nanocarriers with dimensions between 20-50 nm allow enhanced in vivo bioavailability and tumor accumulation, thereby improving the effectiveness of anticancer treatments.…”
supporting
confidence: 78%
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“…This is also a good evidence that PEGylation occurred regioselectively at both GO surfaces.The functionalization of GO sheets with PEG-Fol chains was also established by means of AFM and SEM microscopies (Figure 5).Figure 5ashows a typical dimensional distribution analysis of GO-PEG-Fol, where the presence of GO islands with a thickness of about 3.5 nm and a diameter of about 40 ± 4 nm can be observed. The increase of the nano-flakes thickness of about 2.5 nm can be explained with a homogeneous functionalization of the GO surface with Fol-PEG-CC chains of 2.5 kDa, corroborating UV and FTIR data [5,42]. It might be noticed that the small size and the narrow size distribution observed are suitable for biomedical applications, especially as carrier for anticancer drugs, since nanocarriers with dimensions between 20-50 nm allow enhanced in vivo bioavailability and tumor accumulation, thereby improving the effectiveness of anticancer treatments.…”
supporting
confidence: 78%
“…To the best of our knowledge, prior works have reported IC 50 from 3.4 to 18.25 g mL -1 , confirming that GO-PEG-Fol/Doxo nanoflakes have high pharmacological potency. [5,10,50] The same consideration can be made for MDA-MB-231 cells. [50][51][52] It is noteworthy that, comparable to the effect caused by free Doxo, GO-PEG-Fol/Doxo showed a selective cytotoxicity towards cancer cells, especially for MDA-MB-231.…”
Section: Physicochemical Stability Of Go-peg-fol/doxo In Aqueous Mediamentioning
confidence: 99%
“…A significant in vitro cytotoxic effect on breast cancer cells MDA-MB-231 was shown by GO-methyl acrylate (MA) NPs coated with FA and loaded with paclitaxel (PTX). Moreover, in vivo (in DMBA induced breast cancer rats) studies were performed and demonstrated that treatment with this nanosystem regulates the levels of mitochondrial citric acid enzymes to be near normal [159]. Two-dimensional CS polymerized GO and PVP polymerized GO NPs decorated with FA and loaded with camptothecin (CPT) were prepared by Deb and Vimala.…”
Section: Figure 11mentioning
confidence: 99%
“…Graphene has also been reported as a promising material for various applications ranging from quantum physics, catalysis, and engineering of nanocomposites nanoelectronics to energy research and biomaterials (14)(15)(16)(17). In a nanomedicine realm, graphene and its composites can be employed in different applications including a new generation of biosensors, nanocarriers for drug delivery, and probes for cell and biological imaging (15,(18)(19)(20). During the last two decades, different nanomaterials of various shapes and chemical compositions, including metal and metal oxide nanoparticles, polymeric micelles, liposomes, dendrimers, and carbon nanotubes, have been studied as nanocarriers for drug delivery (21)(22)(23)(24).…”
Section: Introductionmentioning
confidence: 99%