Tuneable catechin functionalisation of carbohydrate polymers
•Catechin was successfully conjugated to three carbohydrate polymers: dextran sodium alginate and chitosan•The degree of catechin functionalisation could be easily tuned by varying the acid concentration in the reaction mixture.•Catechin functionalisation levels of up to 48% were achieved•The struct...
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| Published in | Carbohydrate polymers Vol. 169; pp. 480 - 494 |
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| Main Authors | , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
England
Elsevier Ltd
01.08.2017
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| Subjects | |
| Online Access | Get full text |
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| Abstract | •Catechin was successfully conjugated to three carbohydrate polymers: dextran sodium alginate and chitosan•The degree of catechin functionalisation could be easily tuned by varying the acid concentration in the reaction mixture.•Catechin functionalisation levels of up to 48% were achieved•The structure of all polymers and conjugates was elucidated by 1H, 1H-13C HSQC and DOSY NMR.•All three conjugates showed superior free-radical scavenging activity compared with the non-functionalised polymers.
In this contribution, we present a strategy to functionalise three natural carbohydrate polymers (dextran − a neutral polymer, sodium alginate − an anionic polymer and chitosan − a cationic polymer) with catechin with excellent degrees of functionality. In a first step, the carbohydrate polymers were oxidised by sodium periodate to yield aldehyde functionalised carbohydrate polymers. The presence of aldehyde groups was exploited to attach catechin by an acid catalysed nucleophilic reaction. The degree of catechin functionalisation could be easily tuned by varying the acid concentration in the reaction mixture, achieving catechin functionalisation levels of up to 48% for dextran aldehyde catechin, 35% for chitosan-aldehyde-catechin and 22% for sodium alginate aldehyde catechin. 1H, 1H-13C HSQC and DOSY NMR were performed to elucidate the structural differences between the three aldehyde functionalised polysaccharides and how this affects their reactivity and conjugation behaviour. All three carbohydrate polymer-catechin conjugates showed superior free-radical scavenging activity compared with the non-functionalised polymers. |
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| AbstractList | In this contribution, we present a strategy to functionalise three natural carbohydrate polymers (dextran - a neutral polymer, sodium alginate - an anionic polymer and chitosan - a cationic polymer) with catechin with excellent degrees of functionality. In a first step, the carbohydrate polymers were oxidised by sodium periodate to yield aldehyde functionalised carbohydrate polymers. The presence of aldehyde groups was exploited to attach catechin by an acid catalysed nucleophilic reaction. The degree of catechin functionalisation could be easily tuned by varying the acid concentration in the reaction mixture, achieving catechin functionalisation levels of up to 48% for dextran aldehyde catechin, 35% for chitosan-aldehyde-catechin and 22% for sodium alginate aldehyde catechin.
H,
H-
C HSQC and DOSY NMR were performed to elucidate the structural differences between the three aldehyde functionalised polysaccharides and how this affects their reactivity and conjugation behaviour. All three carbohydrate polymer-catechin conjugates showed superior free-radical scavenging activity compared with the non-functionalised polymers. In this contribution, we present a strategy to functionalise three natural carbohydrate polymers (dextran - a neutral polymer, sodium alginate - an anionic polymer and chitosan - a cationic polymer) with catechin with excellent degrees of functionality. In a first step, the carbohydrate polymers were oxidised by sodium periodate to yield aldehyde functionalised carbohydrate polymers. The presence of aldehyde groups was exploited to attach catechin by an acid catalysed nucleophilic reaction. The degree of catechin functionalisation could be easily tuned by varying the acid concentration in the reaction mixture, achieving catechin functionalisation levels of up to 48% for dextran aldehyde catechin, 35% for chitosan-aldehyde-catechin and 22% for sodium alginate aldehyde catechin. 1H, 1H-13C HSQC and DOSY NMR were performed to elucidate the structural differences between the three aldehyde functionalised polysaccharides and how this affects their reactivity and conjugation behaviour. All three carbohydrate polymer-catechin conjugates showed superior free-radical scavenging activity compared with the non-functionalised polymers. •Catechin was successfully conjugated to three carbohydrate polymers: dextran sodium alginate and chitosan•The degree of catechin functionalisation could be easily tuned by varying the acid concentration in the reaction mixture.•Catechin functionalisation levels of up to 48% were achieved•The structure of all polymers and conjugates was elucidated by 1H, 1H-13C HSQC and DOSY NMR.•All three conjugates showed superior free-radical scavenging activity compared with the non-functionalised polymers. In this contribution, we present a strategy to functionalise three natural carbohydrate polymers (dextran − a neutral polymer, sodium alginate − an anionic polymer and chitosan − a cationic polymer) with catechin with excellent degrees of functionality. In a first step, the carbohydrate polymers were oxidised by sodium periodate to yield aldehyde functionalised carbohydrate polymers. The presence of aldehyde groups was exploited to attach catechin by an acid catalysed nucleophilic reaction. The degree of catechin functionalisation could be easily tuned by varying the acid concentration in the reaction mixture, achieving catechin functionalisation levels of up to 48% for dextran aldehyde catechin, 35% for chitosan-aldehyde-catechin and 22% for sodium alginate aldehyde catechin. 1H, 1H-13C HSQC and DOSY NMR were performed to elucidate the structural differences between the three aldehyde functionalised polysaccharides and how this affects their reactivity and conjugation behaviour. All three carbohydrate polymer-catechin conjugates showed superior free-radical scavenging activity compared with the non-functionalised polymers. |
| Author | Oliver, Susan Boyer, Cyrille Kavallaris, Maria Jofri, Aziidah Thomas, Donald S. Vittorio, Orazio |
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| Keywords | Dextran Sodium periodate Catechin NMR Chitosan Sodium alginate |
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| Snippet | •Catechin was successfully conjugated to three carbohydrate polymers: dextran sodium alginate and chitosan•The degree of catechin functionalisation could be... In this contribution, we present a strategy to functionalise three natural carbohydrate polymers (dextran - a neutral polymer, sodium alginate - an anionic... |
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| SubjectTerms | Carbohydrates - chemistry Catalysis Catechin Catechin - chemistry Chitosan Chitosan - chemistry Dextran NMR Polymers Sodium alginate Sodium periodate |
| Title | Tuneable catechin functionalisation of carbohydrate polymers |
| URI | https://dx.doi.org/10.1016/j.carbpol.2017.04.032 https://www.ncbi.nlm.nih.gov/pubmed/28504171 https://search.proquest.com/docview/1899115309 |
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