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. 2021 Nov 30;13(23):4207. doi: 10.3390/polym13234207

Table 1.

Parameters and conditions tested in the development and optimization of the method.

1-Homogenization Technique 1 N° Formulation Emulsion Observed EE (%)
Ultrasonic Processor
One-time addition, 130 watts, 20 kHertz, 3 mm Ti probe
Sonication Time 30 min 1 No NA
45 min 2 No NA
High Speed Homogenizer
10,000 rpm, 10 min
Mixing phases speed Slow 3 Yes 46
Medium 4 Yes 98
Fast 5 Yes 30
2-Optimization of homogenization technique 1 Emulsion observed EE (%)
High speed homogenizer, mixing phases at medium speed, 10 min Homogenization speed 12,000 rpm 6 Yes 92
16,000 rpm 7 Yes 98
3-Lipid, drug loading, lipid-drug ratio, and organic solvent Emulsion observed EE (%)
Type of lipid 24:1 lipid:drug ratio Cocoa butter 8 Yes 71
Cetyl Palmitate 9 Yes 54
Stearic acid 10 Yes 81
Cholesterol: Cetyl Palmitate 1:1 11 Yes 47
Drug loading mg of CUR 7.5 12 Yes 87
10 13 Yes 62
15 14 No NA
Lipid-drug ratio Chol:CUR 12:1 15 Yes 75
48:1 16 Yes 70
Organic solvent 1:1 solvent mixture CH2Cl2:MeOH 17 Yes 37
CH3Cl3:EtOH 18 Yes 8
4-Surfactant selection and polymer concentration Emulsion observed EE (%)
Surfactant selection 1% surfactant concentration Tween 80 19 No NA
Span 80 20 No NA
Polymer concentration mg/mL of Pluronic F-127 2 21 Yes 5
7 22 Yes 16

NA: Non-applicable; 1 Starting composition: aqueous phase containing 5 mg/mL of Pluronic F-127 in acetic acid 0.1% and Tween 80: Span80 1:1 4% and organic phase containing a CUR-lipid ratio of 1:24 in a 1:1 mixture of MeOH: CHCl3.