The tumor size was calculated using the ellipsoid volume formula: 1/2 × L × W2 [61]. 2.7. Statistics The P values for cytotoxicity and tumor growth were calculated with the Student’s t-test, two tailed by using Graph Pad Software. 3. Results 3.1. Construction and Characterization of Nontargeted and Targeted Liposomes We have previously determined that liposomes composed of DSPG, DSPC, and cholesterol

(molar ratio 1:4:5) form a stable liposomal delivery system [23, Inhibitors,research,lifescience,medical 62, 63]. In addition, the presence of the α1(IV)1263–1277PA did not affect the overall liposome stability. However, the earlier studies utilized ~1% of the α1(IV)1263–1277PA [23], whereas efficient liposome-mediated targeting usually requires 5–23% of the peptide ligand [64–67]. Thus, the present study has examined Inhibitors,research,lifescience,medical the stability and efficacy of liposomes possessing either 5 or 10%α1(IV)1263–1277PA. The liposomes prepared herein also incorporated DSPE-PEG-2000.

The presence of PEG on liposomes allows for increased circulation times in vivo compared to conventional liposomes, which has been attributed to the reduced interactions between the liposomal surface and cells of the reticuloendothelial system (RES) [51–53]. The phospholipid concentration of all Inhibitors,research,lifescience,medical the liposome systems was 0.5mg/mL, as HDAC inhibitor verified by the Stewart Assay [57]. The sizes of the targeted and nontargeted liposomes assembled here were characterized using dynamic light scattering. Liposomes were 84–93nm (small unilamellar vesicles; SUVs) (Table 1), allowing for valid stability comparisons between each system. This size range was previously found to be optimal for efficacious liposomal drug delivery to tumors [68–70]. To confirm the incorporation of the α1(IV)1263–1277PA and DSPE-PEG-2000, liposomes Inhibitors,research,lifescience,medical were treated with ethanol to liberate the α1(IV)1263–1277PA Inhibitors,research,lifescience,medical and PEG from the lipid bilayer. MALDI-TOF mass spectral analysis of the resulting solution produced a peak corresponding to the mass of the α1(IV)1263–1277PA ([M+H]+

= 3813.3Da, theoretical [M+H]+ = 3813.3Da) and a comb-like distribution of peaks corresponding to DSPE-PEG-2000, with the predominant peaks covering [M+H]+ = 1727.9–2122.9Da ([M+H]+ = 1728.8–2123.7Da for DSPE-PEG-2000 directly from the supplier, dissolved in ethanol). UV-visible spectroscopic analysis GPX6 following dialysis indicated 96% incorporation of the PA into liposomes. 3.2. Stability of α1(IV)1263–1277PA to Proteolysis To determine the stability of the α1(IV)1263–1277PA in serum-containing conditions, 17.5μM PA was incubated at 37°C in either (a) water, (b) OptiMEM I media containing 4% FBS, (c) OptiMEM I media containing 10% FBS, 5μg/mL insulin, 5ng/mL epidermal growth factor, and 40μg/mL bovine pituitary extract, or (d) 10% FBS in water. The samples were monitored by RP-HPLC at 0, 24, and 72h. No hydrolysis of the α1(IV)1263–1277PA was observed under these conditions (data not shown).