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. 2019 Mar 26;14:2069–2089. doi: 10.2147/IJN.S190736

Table S1.

Linkage to scFv does not affect liposomal zeta potential or DXR encapsulation

Fresh formulation Size (nm) PDI Zeta (ζ) potential Encapsulation efficiency
DXR-L 86.30±1.34 0.057±0.002 −16.3±0.60 98%
DXR-L scFv G8 94.26±0.66 0.058±0.004 −16±0.70 95%
DXR-L scFv Hyb3 98.30±1.31 0.098±0.02 −16.3±0.49 80%
At 1 week
DXR-L 86.4 0.060 −15.9 97%
DXR-L scFv G8 102.8±1.51 0.073±0.01 −17.6±0.057 94%
DXR-L scFv Hyb3 99.42±1.05 0.083±0.006 −17.6±1.21 77%
At 2 weeks
DXR-L 86.25 0.65 95%
DXR-L scFv G8 104.2±2.46 0.094±0.02 92%
DXR-L scFv Hyb3 99.28±1.50 0.084±0.006 75%
At 4 weeks
DXR-L 86.58±1.42 0.076±0.006 95%
DXR-L scFv G8 106.7±1.81 0.083±0.007 90%
DXR-L scFv Hyb3 107.4±1.15 0.068±0.002 74%

Notes: Three independent batches of three liposome formulations (DXR-L, DXR-L scFv G8, and DXR-L scFv Hyb3) were characterized for size, PDI, surface charge, and encapsulation efficiency for up to 4 weeks (stored in HEPES buffer pH 6.7, at 4°C temperature). Measurements were done in triplicate and are given as average and SD (n=3).

Abbreviations: DXR, doxorubicin; DXR-L, DXR-loaded liposome; PDI, polydispersity index.