“…Release of active ingredient depends on molecular weight, degree of deacetylation, and concentration of chitosan [66,[158][159][160][161][162] Emulsion cross-linking High drug loading efficiency; controlled release with improved bioavailability; and easy to control particle size Tedious process, uses harsh crosslinking agents, problem of reactivity of active agent with cross-linking agent, and challenge of complete removal of unreacted cross-linking agent [40,66,159,161,163] Emulsion-droplet coalescence High loading efficiency and smaller particle size Particle size depends on the degree of deacetylation of chitosan. The decreased degree of deacetylation increases particle size which in turn decreases drug content [66,164] Precipitation Efficient control of particle size and drug release; and avoids the use of toxic organic solvents Partial protection of the loaded active agent from nuclease degradation [40,159] Reverse micellar method Thermodynamically stable particle size with suitable polydispersity index; and narrow size distribution with smaller particle size…”