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. 2019 Nov 29;10:1401. doi: 10.3389/fphar.2019.01401

Table 1.

Mean ( ± SD) of the size (nm), polydispersity index (PDI), zeta potential (mV) and encapsulation efficiency (%EE) of the liposomal formulations developed in this study.

Formulation Size (nm ± SD) PDI ( ± SD) Zeta Potential (mV ± SD) %EE ( ± SD)
LUV 157.53 ± 2.58 0.09 ± 0.03 −19.2 ± 5.5
LUV VAN 152.60 ± 0.80 0.17 ± 0.01* −16.9 ± 0.5 32.5 ± 0.1
LUVfuso 161.87 ± 2.45 0.14 ± 0.02 −48.6 ± 4.9
LUVfuso VAN 153.37 ± 0.70 0.20 ± 0.01* −41.3 ± 2.3* 11.4 ± 0.1
LUVcat 130.97 ± 1.59 0.13 ± 0.01 50.6 ± 3.5
LUVcat VAN 139.73 ± 2.55 0.18 ± 0.02* 62.5 ± 5.6* 10.1 ± 0.1

The asterisk “*” indicates statistically significant difference between plain (LUV, LUVFUSO, LUVCAT) and their respective vancomycin-containing liposomes (LUV VAN, LUVFUSO VAN, LUVCAT VAN), p < 0.05 (unpaired t-test).