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

Figure 1.

Figure 1

BMS/RA@CC-Liposome physicochemical characterization. (A) Size intensity curves of BMS/RA@Liposome (blue), BMS/RA@CC-Liposome (red) and cancer cell membrane vesicles (green) measured by Malvern Zetasizer nano instrument at 25 °C. (B) Hydrodynamic size of BMS/RA@Liposome, BMS/RA@CC-Liposome and cancer cell membrane vesicles. Data are given as mean ± SD (n = 3). (C) Zeta potential of BMS/RA@Liposome, BMS/RA@CC-Liposome and cancer cell membrane vesicles. Data are given as mean ± SD (n = 3). (D) Transmission electron micrographs of (I) a BMS/RA@Liposome; (II) a cancer cell membrane vesicle; (III) a BMS/RA@CC-Liposome; and (IV) multiple BMS/RA@CC-Liposome. All scale bars = 200 nm.