Bi-Functionalized Transferrin@MoS-PEG Nanosheets for Improving Cellular Uptake in HepG2 Cells.

Pre-coating with a protein corona on the surface of nanomaterials (NMs) is an important strategy for reducing non-specific serum protein absorption while maintaining targeting specificity. Here, we present lipoic acid-terminated polyethylene glycol and transferrin bi-functionalized MoS nanosheets (Tf@MoS-PEG NSs) as a feasible approach to enhance cellular uptake. Tf@MoS-PEG NSs can maintain good dispersion stability in cell culture medium and effectively protect MoS NSs from oxidation in ambient aqueous conditions. Competitive adsorption experiments indicate that transferrin was more prone to bind MoS NSs than bovine serum albumin (BSA). It is noteworthy that single HepG2 cell uptake of Tf@MoS-PEG presented a heterogeneous distribution pattern, and the cellular uptake amount spanned a broader range (from 0.4 fg to 2.4 fg). Comparatively, the intracellular Mo masses in HepG2 cells treated with BSA@MoS-PEG and MoS-PEG showed narrower distribution, indicating homogeneous uptake in the single HepG2 cells. Over 5% of HepG2 cells presented uptake of the Tf@MoS-PEG over 1.2 fg of Mo, about three-fold that of BSA@MoS-PEG (0.4 fg of Mo). Overall, this work suggests that Tf coating enhances the cellular uptake of MoS NSs and is a promising strategy for improving the intracellular uptake efficiency of cancer cells.