Nanographene
oxide (NGO) with a non-sheddable poly(
ethylene glycol) (PEG) coating has been used for chemo-
photothermal therapy. However, the drug release of PEGylated NGO (NGO-PEG) with an
amine bond is adversely affected by the diffusion barrier effect of PEG shells. Here, we developed a simple new method for the preparation of biodegradable PEGylated NGO conjugates (NGO-
SS-PEG) with cleavable
disulfide bonds for rapid drug release and more efficiently chemo-
photothermal therapy. The
glutathione (GSH)-induced and photothermal-mediated intracellular release of
doxorubicin (DOX) from NGO-
SS-PEG was studied in A549 cells using confocal
laser scanning microscopy and flow cytometry analysis. In vivo cytotoxicity experiments were performed on chemo-
photothermal therapy. Furthermore, we presented a comparative study of intracellular drug release and
biological efficacy between NGO-
SS-PEG/DOX and NGO-PEG/DOX. The results demonstrated that the rapid drug release from the NGO-
SS-PEG conjugates with sheddable PEG was triggered upon the stimulus of high GSH levels inside A549 cells. Interesting, the DOX release mediated by the photothermal effect from the NGO-
SS-PEG conjugates was found to be more obvious than that for NGO-PEG. Additionally, NGO-
SS-PEG showed a higher efficacy than NGO-PEG for anti-
tumor therapy compared with NGO-PEG. Thus, NGO-
SS-PEG can improve therapeutic efficacy and is an attractive
drug nanocarrier.