2020
DOI: 10.1016/j.jiec.2020.04.030
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Controlling physicochemical properties of graphene oxide for efficient cellular delivery

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Cited by 11 publications
(12 citation statements)
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“…A needle-like GO nanocarrier obtained via conformational change of GO sheets using salt ions in the cell growth medium, was characterized with high surface area and satisfactory number of functional groups for DOX accumulation on the GO sheets. GO needles showed convenable biocompatibility at concentrations <100 μg/mL and after loading with DOX they showed ameliorated anticancer effectiveness compared to free DOX caused by improved cellular endocytosis of a 1D needle structure [ 180 ]. GO co-loaded with both DOX and the apoptotic agent antimiR-21 released rapidly both loaded compounds in cancer cells, resulting in effective destroying of cancer cells, whereby a low DOX dose was sufficient for the inhibition of MDA-MB-231 cells and antimiR-21 caused silencing of miR-21, upregulation of which is associated with numerous types of cancer [ 181 ].…”
Section: Graphene Oxidementioning
confidence: 99%
“…A needle-like GO nanocarrier obtained via conformational change of GO sheets using salt ions in the cell growth medium, was characterized with high surface area and satisfactory number of functional groups for DOX accumulation on the GO sheets. GO needles showed convenable biocompatibility at concentrations <100 μg/mL and after loading with DOX they showed ameliorated anticancer effectiveness compared to free DOX caused by improved cellular endocytosis of a 1D needle structure [ 180 ]. GO co-loaded with both DOX and the apoptotic agent antimiR-21 released rapidly both loaded compounds in cancer cells, resulting in effective destroying of cancer cells, whereby a low DOX dose was sufficient for the inhibition of MDA-MB-231 cells and antimiR-21 caused silencing of miR-21, upregulation of which is associated with numerous types of cancer [ 181 ].…”
Section: Graphene Oxidementioning
confidence: 99%
“…[139] However, a previous study showed that despite having a large length, some needle-like GBMs (length of 1.1 mm) can efficiently internalize into the cytoplasm of human dermal fibroblast cells. [140] By labeling GO with gold NMs and tracing them using surfaceenhanced Raman scattering spectroscopy, Huang et al documented that GO can enter Ca Ski (human cervix (small bowel metastasis)) cells mainly through clathrin-mediated, energydependent endocytosis and distribute inside the cells. [27] A small variation in lateral size could result in a big difference in the pathway through which GBMs enter cells.…”
Section: Cellular Uptakementioning
confidence: 99%
“…Functionalization of graphene NMs with hydrophilic functional groups such as hydroxyl and carboxyl groups can facilitate their dispersion in physiological media. [140,151] Zhang et al applied sulfonic acid and folic acid groups for stabilization of GO NMs under physiological conditions. [152] However, there are some challenges associated with the functionalization of graphene sheets to increase their dispersion in physiological media.…”
Section: Cellular Uptakementioning
confidence: 99%
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