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Amorphous solid dispersion studies of camptothecin-cyclodextrin inclusion complexes in PEG 6000

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Figure

Figure 1. CPT structure (active and inactive form) (9)
Table 1. Solubility and equilibrium constants (Kc) for camptothecin complexes calculated from the slope of the best-fit line of the phase solubility.
Figure 5. Solubility diagrams of camptothecin in the presence of SBE-β-CD and PM-β-CD
Figure 6. Camptothecin kinetic release from SDs at 5/95, 10/90, 15/85, 30/70 (w/w) percentages
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