Figures & data
Figure 1 FT-IR spectra of chitosan 5k (red) and O-palmitoyl chitosan (black).
Abbreviations: FT-IR, Fourier transform infra-red; T, transmittance.
![Figure 1 FT-IR spectra of chitosan 5k (red) and O-palmitoyl chitosan (black).Abbreviations: FT-IR, Fourier transform infra-red; T, transmittance.](/cms/asset/eca48f54-f71d-4ce3-bb3c-c5805222edfc/dijn_a_12194115_f0001_c.jpg)
Figure 3 DSC thermogram of (A) chitosan (50°C/min) and (B) O-palmitoyl chitosan (20°C/min).
Abbreviation: DSC, differential scanning calorimetry.
![Figure 3 DSC thermogram of (A) chitosan (50°C/min) and (B) O-palmitoyl chitosan (20°C/min).Abbreviation: DSC, differential scanning calorimetry.](/cms/asset/f1e85824-6d82-4cf4-9a0e-097aef8759fd/dijn_a_12194115_f0003_b.jpg)
Figure 4 X-ray powder diffractograms of (A) chitosan and (B) O-palmitoyl chitosan.
Abbreviations: ADUs, analog digital units; deg, degrees.
![Figure 4 X-ray powder diffractograms of (A) chitosan and (B) O-palmitoyl chitosan.Abbreviations: ADUs, analog digital units; deg, degrees.](/cms/asset/3ced95bc-67c7-4e0e-a5cd-1fda1866cd30/dijn_a_12194115_f0004_c.jpg)
Table 1 Particle size distribution, surface charge, and entrapment efficiencies for liposome preparations
Figure 5 Caco-2 cell viability assessed by MTT assay following (A) 48 hours and (B) 72 hours incubation with liposome formulations containing increasing drug concentrations (mean±SD, n=6).
![Figure 5 Caco-2 cell viability assessed by MTT assay following (A) 48 hours and (B) 72 hours incubation with liposome formulations containing increasing drug concentrations (mean±SD, n=6).](/cms/asset/920e9f65-afe1-4dc4-9110-4d8c41f7155c/dijn_a_12194115_f0005_b.jpg)
Figure 6 Iron absorption by Caco-2 cells incubated with liposome formulations: intracellular ferritin was measured as a marker of iron absorption by ELISA following 22 hours of incubation after iron uptake experiments.
Note: Results are shown as mean±SD (n=6), *Represents a significant difference (95%) between treatment and FeSO4 alone. ^Represents a significant difference (95%) between OPC liposomes and liposomes alone.
![Figure 6 Iron absorption by Caco-2 cells incubated with liposome formulations: intracellular ferritin was measured as a marker of iron absorption by ELISA following 22 hours of incubation after iron uptake experiments.Note: Results are shown as mean±SD (n=6), *Represents a significant difference (95%) between treatment and FeSO4 alone. ^Represents a significant difference (95%) between OPC liposomes and liposomes alone.](/cms/asset/a453108c-c1f3-45fa-819c-4b4406b1e9c6/dijn_a_12194115_f0006_b.jpg)
Figure 7 Confocal microscopy images of Caco-2 cells following incubation with coumarin-6 loaded (A–C) conventional (Lipo-Cou) liposomes and (D–F) OPC liposomes (OPC-Lipo-Cou).
Notes: Images (A and D) demonstrate cell nuclei stained with TO-PRO-3 (blue), images (B and E) show cell cytoplasm with accumulated liposomal coumarin-6, and images (C and F) show merged images. Scale shown is 50 µM.
![Figure 7 Confocal microscopy images of Caco-2 cells following incubation with coumarin-6 loaded (A–C) conventional (Lipo-Cou) liposomes and (D–F) OPC liposomes (OPC-Lipo-Cou).Notes: Images (A and D) demonstrate cell nuclei stained with TO-PRO-3 (blue), images (B and E) show cell cytoplasm with accumulated liposomal coumarin-6, and images (C and F) show merged images. Scale shown is 50 µM.](/cms/asset/822ee80e-cc39-453c-81a0-452fe1e57a0a/dijn_a_12194115_f0007_c.jpg)