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. 2021 Oct 22;12(4):2103–2119. doi: 10.1016/j.apsb.2021.10.010

Figure 3.

Figure 3

Investigation of anti-phagocytosis capability and homologous adhesion property of BMS/RA@CC-Liposome. (A) Intracellular uptake of BMS/RA@Liposome in RAW264.7 cells after 1–2 h incubation. The nucleus was stained with Hoechst 33342 (blue). The BMS/RA@Liposome was labeled with Cy5.5 (red). Scale bar = 10 μm. (B) Intracellular uptake of BMS/RA@CC-Liposome in RAW264.7 cells after 1–2 h incubation. The nucleus was stained with Hoechst 33342 (blue). The BMS/RA@CC-Liposome was labeled with Cy5.5 (red). Scale bar = 10 μm. (C) Intracellular uptake of BMS/RA@RBC-Liposome in RAW264.7 cells after 1–2 h incubation. The nucleus was stained with Hoechst 33342 (blue). The BMS/RA@RBC-Liposome was labeled with Cy5.5 (red). Scale bar = 10 μm. (D) Intracellular uptake of BMS/RA@CC-Liposome in CT26, HCT116, SW620, RKO and A549 cells after 3 h incubation. The nucleus was stained with Hoechst 33342 (blue). The BMS/RA@CC-Liposome was labeled with Cy5.5 (red). Scale bar = 10 μm. (E) Quantitative analysis of BMS/RA@CC-Liposome uptake with CT26, HCT116, SW620, RKO and A549 cells. Data are given as mean ± SD (n = 3). ∗∗∗P < 0.001.