The development of non-viral vectors for gene delivery has primarily focuse
d on improving the efficiency of gene transfer in vivo. Although there is c
learly a need to improve delivery efficiency, studies also indicate that th
e physical stability of non-viral vectors is not nearly adequate for a mark
etable pharmaceutical product. Here, we describe the different strategies t
hat have been used to enhance stability and discuss the mechanisms by which
prolonged stabilization (>2 years) might be achieved.