Interestingly, immediately after treatment, cell death was most dependent on Optison; however, 24h after treatment, cell death was more dependent on 5-FU,
and the best minimal effective dose for cell killing was 10μg/mL. Furthermore, treatment with 5-FU and US increased the levels of Bax and p27kip1 proapoptotic proteins, but the addition of Optison appeared to suppress apoptotic protein expression. This study clearly illustrates the need for experimental design aimed at dissociating specific from nonspecific toxicity effects of a gene or drug delivered Inhibitors,research,lifescience,medical by sonoporation in order to better refine the conditions for Selleck MG 132 delivery in vivo. Another detailed study that illustrated the importance of examining the best parameters for delivering macromolecules used a macromolecule that modeled the Mw of drugs Inhibitors,research,lifescience,medical or plasmid
DNA and delivery with Optison [1, 30], whereby transfection was obtained up to ~37% with minimal cell death, identifying optimal parameters of US exposure able to produce efficient delivery of macromolecules. Like MBs, in our experience, echogenic nanoparticles made from polystyrene (PS) or PLGA also do not appear Inhibitors,research,lifescience,medical to produce any toxic effects in the presence of US. For example, in an in vivo DU145 prostate cancer model, no alterations are seen histologically to indicate cell death in tissues for PLGA NP plus US, even in the presence of pDNA:PEI complexes [3]. The next section will cover in detail strategies for US-mediated DNA delivery with PLGA and PEI:pDNA NP in vivo. 3.1.3. Ultrasound Enhances Gene Delivery by PLGA When pDNA Is Complexed with Polycationic Polymers Over the years, a significant number of cationic polymers have been explored as carriers for gene delivery (reviewed in [33]) since they condense DNA into small particles and facilitate Inhibitors,research,lifescience,medical uptake by endocytosis. One of these cationic polymers is poly(ethylene imine) or PEI (reviewed in [34]). The potential of PEI was first described for gene delivery applications in 1995 [35]. Several molecular weights of PEI have been investigated with Inhibitors,research,lifescience,medical the most suitable
forms ranging in 5–25kDa [36, 37]. Higher-molecular-weight PEI increases cytotoxicity due to polymer Carnitine dehydrogenase aggregation at the cell surface [38]. Low-molecular-weight PEI is less toxic yet is usually less effective for gene delivery, since the lower amount of positive charges per molecule makes it difficult for small PEIs to appropriately condense negatively charged DNA molecules. Gene delivery research has used either hyperbranched or linear PEI, and branched PEI has shown stronger complexation with DNA since it typically forms smaller complexes DNA:linear PEI [39]. The condensation behavior of branched PEI:DNA is less dependent on buffering than high-molecular-weight PEI, yet the transfection efficiency of linear PEI (22kD):DNA complexes is typically higher than that of branched PEI (25kD) when prepared in a salt-containing buffer [39].