The importance of nanoparticle properties that on one hand ensure systemic stability by having a PEG layer on the surface and on the other hand are able to transfect cells with great efficiency once the nanoparticle has arrived at its target site has been discussed in many papers (e.g. Hatakeyama et al. [23]. One of the most promising

strategies involve stabilized plasmid lipo-particles [10] using custom-designed lipid components including PEGylated [24] and cationic lipids [25]. Here we tested a formulation of similar properties from commercially available lipids to assess nanoparticle properties, systemic stability, transfection efficiency and usefulness in a http://www.selleckchem.com/products/ly2157299.html suicide gene therapy application.

We have previously described the efficient encapsulation of plasmid DNA into PEGylated immuno-liposomes with 70% of the plasmid being encapsulated in the interior [9] and while using similar procedures we obtained SPLPs in approximately 150 nm in size. In addition to PicoGreen assay, agarose gel electrophoresis provide a method for evaluating the encapsulation and externally bound plasmid DNA [9], [15] and [16], and hence we found that plasmid DNA was effectively encapsulated and protected from nucleases Selleckchem PF01367338 (Fig. 1) and could be applied to cells and animals without further purification. A nuclease digestion and subsequent purification by size-exclusion chromatography did not change the size of the particles, but merely caused

an unfavorable dilution of the SPLPs. Furthermore, we measured unchanged luciferase activity in vitro when analyzing nuclease-treated SPLPs; however, concerns of systemic immune responses to nucleic acids [26] and [27] or C-p-G [28]in vivo persist and could favor additional steps of SPLP purification [9] and [20]. When we analyzed the luciferase activities of SPLPs with encapsulated luciferase reporter plasmid we found considerable activities in human non-small cell lung cancer H1299 cells. In small cell lung cancer NCI-H69 cells the luciferase activity was much lower (Fig. 2). Presumably, this difference reflects growth properties and internalization capabilities of the two cell lines and has been found with a number of different lipid-based transfection ADAMTS5 reagents [13] and [21] (unpublished data). Nevertheless xenograft tumors derived from NCI-H69 cells growing on the flank of nude mice could be transfected with our SPLPs by intravenous delivery, as we measured a moderate reporter activity (Fig. 4) comparable to the results of others [10]. This finding could relate to the fact that tumor cells that are actively dividing have fewer intracellular barriers to successful SPLP-mediated transfection than other diffentiated tissues analyzed. Furthermore, in lung tissue we measured luciferase activity above background level, although only a low amount of SPLP resided in the lung (2–3%, Fig. 5).