Following manufacturer’s recommendations, reverse transfection in medium with serum was performed, though direct transfection was first evaluated but without success. To evaluate cellular uptake, fluorescent dsRNA and the lecithin dispersions were mixed and incubated 20 minutes; for control experiments, Lipofectamine was also mixed with the dsRNA and assayed in parallel. The dsRNA:lecithin complexes, the control dsRNA:Lipofectamine control complex, and dsRNA alone were then added to 24-well plates Inhibitors,research,lifescience,medical prior to the addition of 2 × 105 MCF-7 cells per well. Cells were incubated 18 hours at 37°C in a CO2 incubator, being then washed and fixed and the fluorescence

signal detected using fluorescence microscopy. 2.8. Stability of the Nanoparticles The lecithin-based dispersions prepared as previously described were sealed into glass vials and stored at room temperature in the dark for one month. The size of the particles was Inhibitors,research,lifescience,medical measured by PCS on day 0 and after one month of storage. 2.9. Statistical Analyses Statistical analyses were carried out using one-way analysis of variance (ANOVA) in GraphPad InStat 3.01 for Windows. For cytotoxicity data evaluation, ANOVA was selleck inhibitor followed Inhibitors,research,lifescience,medical by the Dunnett multiple comparisons test procedure against control. A P value of ≤0.05 (two tailed) was considered to be statistically significant.

3. Results and Discussion In order to evaluate the siRNA loading capacity of the formulations, the appropriate diluent was first selected. For this purpose, aqueous soybean lecithin dispersions were prepared in different media, and binding between siRNA and

Inhibitors,research,lifescience,medical dispersed lecithin was analyzed by agarose gel retardation assay. As it is shown in Figure 1, lecithin bound the oligonucleotide when dispersed in pH 5.0 and pH 7.0 buffers, but was unable to assemble when dispersed in water or glycerol. The same results were obtained for all the different lecithin concentrations tested. Figure 1 Gel retardation assay of formulations in different Inhibitors,research,lifescience,medical media (a: water, b: glycerol 2.76%w/w, c: pH 5.0 buffer, d: pH 7.0 buffer). Control assay involved siRNA alone (−) or is associated to Lipofectamine (+). (Upper bands: bound siRNA). Being unsuitable diluents disregarded, dispersions in pH 5.0 and pH 7.0 buffers were then loaded with siRNA at different N/P ratios and analyzed by means of the same assay. Results already demonstrated that lecithin is assembled with siRNA in a broad range of N/P ratios, especially above 1000 (Figure 2). Meanwhile, it is to remark that only lecithin dispersed in pH 5.0 buffer was able to at least weakly associate at much lower ratios, whereas at pH 7.0, binding was not observed below N/P 100. This fact can be related to the higher proportion of the positively charged form of the phosphocholine polar head at lower pH values, supported by the zeta potential results which are later presented and discussed.