“…It has to be noted that a lot of work has been done on liposome-polyelectrolyte complexation by employing DNA, which is quite different in terms of flexibility with respect to NaPA, which has approximately the same charge density but a much higher flexibility, and a coexistence of different structures ranging from multilamellar DNA lipid complexes to unilamellar DNA-coated vesicles, as pd-liposome aggregates, has been observed [40,4]. Within this framework, similarly to what observed in the presence of DNA by several authors (see for example [13,41] and references therein), our results further confirm the ability to tune structure and morphology of the aggregates by means of lipid composition, ionic strength and polymer/lipid charge ratio. Moreover, due to the good biocompatibility of NaPA [42,43], the DOTAP/DOPC-NaPA complexes have also a specific interest for their potential use as multi-compartment vectors for multi-drug delivery [9].…”