“…The examples of such microparticles produced using MCE are polymer microspheres (Sugiura et al, 2001;Sugiura et al, 2002d), gel microbeads (Iwamoto et al, 2002;Sugiura et al, 2005;Ikkai et al, 2005;Chuah et al, 2009), solid lipid microparticles (Sugiura et al, 2000;Kobayashi et al, 2003b), complex coacervate microcapsules (Nakagawa et al, 2004), and giant lipid vesicles (Kuroiwa et al, 2009). MC array devices have also been used for production of monodispersed microbubbles (Yasuno et al, 2004), discoid droplets (Kobayashi et al, 2006), surfactant-free droplets stabilized by silica nanoparticles (Xu et al, 2005c) and oil droplets stabilised by lecithin-chitosan interfacial bilayers (Chuah et al, 2009b). Because of its ability to generate monodisperse droplets of tunable size on a larger scale than planar microfluidic devices, MCE is a usuful technique for fundamental studies on emulsions, for example studies of emulsion stability (Liu et al, 2001), crystallisation of emulsion droplets (Hamada et al, 2002), in vitro digestability of emulsified lipids, etc.…”