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. 2013 Jan;34(4):1179–1192. doi: 10.1016/j.biomaterials.2012.09.070

Table 2.

Compositions of liposomes labeled with 64Cu (HK) and 111In (L–P). Liposomes H, I, L, M and N were formulated using DEG3SL 16 then labelled with 64Cu or 111In post-formulation. Liposomes J, K, O and P were formulated using DEG6SL 17 then labelled with 64Cu or 111In post-formulation. Liposomes Q and R were formulated as controls lacking the DOTA-lipids. Samples L, N, O and P were used for in vivo biodistribution.

Liposome DOPE Cu/In-lipid PEG-lipid DOTMA FL-DHPE DLS (PDI) Zeta
H 10% 30% Cu-DEG3SL 50% DODEG4 10%
I 10% 30% Cu-DEG3SL 60%
J 10% 30% Cu-DEG6SL 50% DODEG4 10%
K 10% 30% Cu-DEG6SL 60%
L 9% 30% In-DEG3SL 50% DODEG4 10% 1% 73.9 nm (0.2) (+) 54 mV
M 10% 30% In-DEG3SL 60%
N 2% 30% In-DEG3SL 7% DSPE-PEG2000 60% 1% 141.7 nm (0.2) (+) 43 mV
O 9% 30% In-DEG6SL 50% DODEG4 10% 1% 70.1 nm (0.2) (+) 50 mV
P 2% 30% In-DEG6SL 7% DSPE-PEG2000 60% 1% 142.6 nm (0.2) (+) 31 mV
Control Q 40% 50% DODEG4 10%
Control R 50% 50%