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. Author manuscript; available in PMC: 2018 Oct 19.
Published in final edited form as: Nanoscale. 2017 Oct 19;9(40):15379–15389. doi: 10.1039/c7nr02327h

Figure 5.

Figure 5

In vitro DOX delivery and analysis. (a) MOS-J osteosarcoma normalized mitochondrial activity or viability after exposure to various concentrations of DOX. IC50 of DOX was observed to be at concentrations above 10 µg/mL. (b) Live/Dead staining of MOS-Js revealed a greater number of dead cells when exposed to free DOX as compared to DOX-loaded nanogels and nanocomposites (Scale bar 100µm). (c) MTT assay of MOS-Js exposed to various experimental groups. DOX-loaded nanogels significantly increased (***p<0.001) cell viability in comparison to free DOX. Additionally, incorporation of DOX-loaded nanogels in the GelMA matrix further increased cell viability. (d) MC3T3s were also exposed to free DOX and DOX-loaded nanogels and a similar response in cell viability was observed (Scale bar 100µm). (e) comparison of MC3T3 viability of various experimental groups normalized to untreated control. A significant increase (***p<0.001) in cell viability was observed in the DOX-loaded nanogels.