Synthesis and enzymatic degradation of epichlorohydrin cross-linked pectins |
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Authors: | Semdé Rasmané Moës André J Devleeschouwer Michel J Amighi Karim |
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Affiliation: | a Laboratory of Pharmaceutics and Biopharmaceutics, UFR/SDS, University of Ouagadougou, Ouaga, Burkina Fasob Laboratory of Pharmaceutics and Biopharmaceutics, Pharmacy Institute, Free University of Brussels, Brussels, Belgiumc Laboratory of Microbiology and Hygiene, Pharmacy Institute, Free University of Brussels, Brussels, Belgium |
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Abstract: | The water solubility of pectin was successfully decreased by cross-linking with increasing amounts of epichlorohydrin in the reaction media. The initial molar ratios of epichlorohydrin/ galacturonic acid monomer in the reaction mixtures were 0, 0.37, 0.56, 0.74, 1.00, 1.47, and 2.44. The resulting epichlorohydrin cross-linked pectins were thus referred to as C-LP0, C-LP37, C-LP56, C-LP75, C-LP100, C-LP150, and C-LP250, respectively. Methoxylation degrees ranged from 60.5 ± 0.9% to 68.0 ± 0.6%, and the effective cross-linking degrees, determined by quantification of the hydroxyl anions consumed during the reaction, were 0, 17.8, 26.0, 38.3, 46.5, 53.5, and 58.7%, respectively. After incubating the different cross-linked pectins (0.5% w/v) in 25 mL of 0.05 M acetate-phosphate buffer (pH 4.5), containing 50 µL of Pectinex® Ultra SP-L (pectinolytic enzymes), between 60 and 80% of the pectin osidic bounds were broken in less than 1 hr. Moreover, increasing the cross-linking degree only resulted in a weak slowing on the enzymatic degradation velocity. |
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Keywords: | Epichlorohydrin Cross-linked pectins Colonic drug delivery Enzymatic degradation |
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