“…13,17,18 Although chitosan-coated liposomes are starting to be produced for the delivery of several types of active molecules (e.g., diclofenac sodium, leuprolide, superoxide dismutase, indomethacin, alkaloids, and other types of molecules with therapeutic properties [18][19][20][21][22][23] ), the processes which lead to their production remain at the bench-scale, leading to small product volumes in output. Up to now, the methods usually employed for liposome covering by chitosan are based essentially on dropwise bulk methods 13,18,[24][25][26][27][28][29] such as the layer-bylayer (LbL) method. 30,31 Some efforts have been made towards improvement of these conventional methods using, for example, a supercritical reverse-phase evaporation method, 32 by exploiting complex and expensive apparatus.…”