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Beilstein J. Org. Chem. 2023, 19, 78–88, doi:10.3762/bjoc.19.7
Graphical Abstract
Figure 1: Quillaja saponin foamability (left) and foam stability over time for the β-cyclodextrin/polysacchar...
Figure 2: SEM images of crushed β-c-LBG as a function of the synthesis pathways (see below, Experimental sect...
Figure 3: SEM of β-csp after crosslinking with or without washing the sample.
Figure 4: β-csp (left) and c-CSsp (right) matrices unwashed showing the “foam-like” morphologies.
Figure 5: Values (in mg/g) of equivalent ‘free β-cyclodextrin’ in the polysaccharide (PS) matrices, as a func...
Figure 6: 1-Naphthol isotherms of crosslinked β-cyclodextrin/polysaccharides (blue curves for chitosan, red f...
Figure 7: Sorption of phenols (V, vanillin; Ph, phenol; m-c, m-cresol; 4eP, 4-ethylphenol; Eu, eugenol) in β-...
Figure 8: Six synthesis routes (*lyophilized matrices) used to prepare samples β-c-XGsp; β-c-LBGsp; β-c-CSsp ...
Beilstein J. Org. Chem. 2014, 10, 3127–3135, doi:10.3762/bjoc.10.330
Figure 1: Inclusion complex (polypseudorotaxane) between α-cyclodextrins and reverse Tetronics.
Figure 2: 90R4/α-CD gels loaded with lactase. Octablock Tetronic molecules (grey) are threaded by CDs (red) f...
Figure 3: FTIR spectra of Tetronic 90R4, α-CD, lactase and T25a10 complex.
Figure 4: Release profiles of lactase from T25a10 (open circles) and T15a10 (filled circles) at pH 6 from a) ...
Figure 5: Contribution of diffusion (open circles) and erosion (filled circles) mechanisms from polymers a) T...
Figure 6: Chemical structure of a reverse Tetronic.