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. 2023 Dec 13;10(1):e23637. doi: 10.1016/j.heliyon.2023.e23637

Table 2.

Microencapsulation formulations of l-Carnitine base using emulsion solvent evaporation method.

Trial No. Polymer Viscosity grade Drug/Polymer Ratio Anti-coalescent mixing speed Span 80 (%)
F1 EC N100 3:1 500 0.1
F2 EC N100 3:1 Aerosil 200 500 0.1
F3 EC N100 3:1 Mg stearate 500 0.1
F4 EC N100 3:1 Aerosil 200 1000 0.1
F5 EC N100 3:1 Aerosil 200 1500 0.1
F6 EC N100 3:1 Aerosil 200 1000
F7 EC N100 3:1 Aerosil 200 1000 0.25
F8 EC N100 3:1 Aerosil 200 1000 0.5
F9 EC N100 3:1 Aerosil 200 1000 1
F10 EC N100 4:1 Aerosil 200 1000 0.1
F11 EC N100 2:1 Aerosil 200 1000 0.1
F12 EC N100 1:1 Aerosil 200 1000 0.1
F13 Ethocel Std. 20 4:1 Aerosil 200 1000 0.1
F14 Ethocel Std. 20 3:1 Aerosil 200 1000 0.1
F15 Ethocel Std. 20 2:1 Aerosil 200 1000 0.1
F16 Ethocel Std. 20 1:1 Aerosil 200 1000 0.1

F1, F2, and F3 represented the study of the Anti-coalescent type factor. From that stage, F2 succeeded to continue. F2, F4, and F5 demonstrated the mixing speed variable in the second-stage, from which F4 showed superiority. The study of the effect of emulsifier concentration (on F4, F6, F7, F8, and F9) in the third stage resulted in the choice of F4.