Figures & data
Table 1 Composition of Biorelevant Media Used During in vitro Lipolysis
Figure 1 Solubility of rosuvastatin in different oils and surfactants. Each value shows the mean ± SD (n=3).
![Figure 1 Solubility of rosuvastatin in different oils and surfactants. Each value shows the mean ± SD (n=3).](/cms/asset/14561ddb-cccd-48a0-a666-96082fbe1c2f/dijn_a_12192197_f0001_c.jpg)
Table 2 Nanoemulsion Region with Different Co-Surfactants
Figure 3 Ternary phase diagram of Capmul MCMEP, tween 20 and transcutol P at Smix ratios (A) 1:1, (B) 2:1, (C) 1:2, and (D) 1:3. The colored region (black) represents nano-emulsion formation region.
![Figure 3 Ternary phase diagram of Capmul MCMEP, tween 20 and transcutol P at Smix ratios (A) 1:1, (B) 2:1, (C) 1:2, and (D) 1:3. The colored region (black) represents nano-emulsion formation region.](/cms/asset/f03a8e9d-7dc6-45fc-b02d-e3c9c63e9bbd/dijn_a_12192197_f0003_b.jpg)
Table 3 Composition of Various SNEDDS Formulations Suggested by Design Expert® and Their Responses
Figure 4 Various 2-D counter plots for response: (A) globule size, (B) % CDR, and (C) self-emulsification time.
![Figure 4 Various 2-D counter plots for response: (A) globule size, (B) % CDR, and (C) self-emulsification time.](/cms/asset/cda3daa1-3279-444c-8ca3-a15e099043d6/dijn_a_12192197_f0004_c.jpg)
Table 4 Results of ANOVA
Figure 6 DSC spectra of (A) pure rosuvastatin, (B) physical mixture of drug and excipients, and (C) optimized SNEDDS formulation.
![Figure 6 DSC spectra of (A) pure rosuvastatin, (B) physical mixture of drug and excipients, and (C) optimized SNEDDS formulation.](/cms/asset/47ceea9c-bd64-4a57-9538-46748dc4d50c/dijn_a_12192197_f0006_b.jpg)
Figure 7 FT-IR spectrum of (A) pure rosuvastatin, (B) physical mixture of drug and excipients, and (C) optimized SNEDDS formulation.
![Figure 7 FT-IR spectrum of (A) pure rosuvastatin, (B) physical mixture of drug and excipients, and (C) optimized SNEDDS formulation.](/cms/asset/b535bf23-77a5-4b28-af82-dd4e5818eaeb/dijn_a_12192197_f0007_c.jpg)
Figure 9 Dissolution (multi-media) testing of rosuvastatin SNEDDS. Each value represents the mean ± SD (n=3).
![Figure 9 Dissolution (multi-media) testing of rosuvastatin SNEDDS. Each value represents the mean ± SD (n=3).](/cms/asset/f57c5725-031d-40fd-b3d8-3b8374fe6a13/dijn_a_12192197_f0009_c.jpg)
Figure 10 Comparative dissolution study (pH 6.6 citrate buffer) of rosuvastatin-loaded SNEDDS, pure drug and marketed tablet. Each value represents the mean ± SD (n=3).
![Figure 10 Comparative dissolution study (pH 6.6 citrate buffer) of rosuvastatin-loaded SNEDDS, pure drug and marketed tablet. Each value represents the mean ± SD (n=3).](/cms/asset/bb7a5edb-3d74-443b-a8ba-307b72653da6/dijn_a_12192197_f0010_c.jpg)
Table 5 Stability Data of Optimized Rosuvastatin SNEDDS Formulation (n=6)
Table 6 Lipid Profile in Experimental Animals with Mean± Std. Deviation (n=6)