The liposome sample was prepared by a negative staining method. Phosphotungstic acid (PTA) was deposited on the periphery of the liposome, making the liposome and its background a strong contrast. Then, 0.2 g of PTA powder was dissolved in 20 mL ddH2O in a dark environment. A total of 5 µL liposome solution was dropped on the copper mesh and dried for 5 min. Then, 5 µL of PTA were then added and incubated for 8 min to allow heavy metals to settle around the liposome. A TEM (JEM-1400, JOEL, Tokyo, Japan) was employed to observe the morphology of the liposome.
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