2000
DOI: 10.1590/s0104-14282000000300012
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Preparation and structural characterization of O-acetyl agarose with low degree of substitution

Abstract: Among the biodegradable polymers, the polysaccharides have been found to be promising carriers for bioactive molecules. From a general standpoint, they present several reactive groups, such as hydroxyl, carboxyl and amine, that can be modified in a number of ways, giving rise to suitable devices for controlled release. In this paper, agarose was submitted to O-acetylation reactions under heterogeneous conditions, using acetic anhydride and pyridine, aiming to observe the effect of acetyl groups on the agarose … Show more

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Cited by 29 publications
(10 citation statements)
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“…in the primary amine of chitosan (Figure 2a) [14] , but they were weaken in chitosan-agarose microspheres and the new absorption band at 1650 cm -1 appeared (Figure 2d), which could be attributed to the interaction between the -CHO groups of glutaraldehyde and the -NH 2 groups of chitosan in microspheres [15] . As shown in Figure 2b, the characteristic absorption bands of agarose were observed at 1076 cm -1 (C-O, axial deformation), 933 cm -1 (characteristic of 3, 6-anhydrogalactose) and 889 cm -1 (attributed to C-H angular deformation of anomeric carbon) [16] . Pure berbamine spectra showed the characteristic absorption bands at 1515, 1275 and 1117 cm -1 (Figure 2c) [17] , which also appeared in the spectra of berbamine loaded chitosan-agarose microspheres (Figure 2e) at the same wavenumbers suggesting no interactions between the drug and the carrier.…”
Section: Evaluation Of In Vitro Drug Releasementioning
confidence: 93%
“…in the primary amine of chitosan (Figure 2a) [14] , but they were weaken in chitosan-agarose microspheres and the new absorption band at 1650 cm -1 appeared (Figure 2d), which could be attributed to the interaction between the -CHO groups of glutaraldehyde and the -NH 2 groups of chitosan in microspheres [15] . As shown in Figure 2b, the characteristic absorption bands of agarose were observed at 1076 cm -1 (C-O, axial deformation), 933 cm -1 (characteristic of 3, 6-anhydrogalactose) and 889 cm -1 (attributed to C-H angular deformation of anomeric carbon) [16] . Pure berbamine spectra showed the characteristic absorption bands at 1515, 1275 and 1117 cm -1 (Figure 2c) [17] , which also appeared in the spectra of berbamine loaded chitosan-agarose microspheres (Figure 2e) at the same wavenumbers suggesting no interactions between the drug and the carrier.…”
Section: Evaluation Of In Vitro Drug Releasementioning
confidence: 93%
“…The spectra obtained then calculated its DS value by following the Garcia and Vidal equation below [10] :…”
Section: Characterization Of Modified Starch Cassava Peel Wastementioning
confidence: 99%
“…The results of esterification reaction are analyzed by infrared spectrophotometry. Based on research Garcia and Vidal [14], the DS value was determined by FTIR spectra with the formula:…”
Section: Esterification Reaction With Time Variation Of Ultrasonicationmentioning
confidence: 99%