Synthesis and antioxidant activity evaluation of novel broom and cotton fibers derivatives
Novel antioxidant biopolymers composed by broom or cotton fibers, and trans-ferulic acid, α-lipoic acid, and α-tocopherol, were prepared. The acids were directly linked to fibers microfibrils hydroxylic groups using N,N-dimethylacetamide/lithium chloride (DMAc/LiCl) as solvent with dicyclohexylcarbo...
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| Published in | Journal of applied polymer science Vol. 114; no. 5; pp. 3177 - 3183 |
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| Main Authors | , , , , , , |
| Format | Journal Article |
| Language | English |
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Hoboken
Wiley Subscription Services, Inc., A Wiley Company
01.12.2009
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| Abstract | Novel antioxidant biopolymers composed by broom or cotton fibers, and trans-ferulic acid, α-lipoic acid, and α-tocopherol, were prepared. The acids were directly linked to fibers microfibrils hydroxylic groups using N,N-dimethylacetamide/lithium chloride (DMAc/LiCl) as solvent with dicyclohexylcarbodiimide (DCC) and N,N-dimethylaminopyridine (DMAP). Broom or cotton tocopherulate were prepared in the same conditions by using carboxylated fibers. Ester linkages were confirmed by using Fourier transformed infrared spectroscopy; biopolymers substitution degrees (DS) were determined by volumetric analysis. Antioxidant activity in inhibiting lipid peroxidation, in rat-liver microsomal membranes, induced in vitro by two different sources of free radicals, 2,2'-azobis (2-amidinopropane) (AAPH) and tert-butyl hydroperoxide (tert-BOOH), was evaluated. Finally, biocompatibility of these biomaterials was also tested by controlling glutathione-S-transferase (GST) basal concentrations. Our results strongly suggested that the better derivatives were the ferulate ones. However, all obtained biomaterials, showing excellent antioxidant properties and biocompatibility, could be successfully applied in biomedical and in packaging areas. |
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| AbstractList | Novel antioxidant biopolymers composed by broom or cotton fibers, and trans‐ferulic acid, α‐lipoic acid, and α‐tocopherol, were prepared. The acids were directly linked to fibers microfibrils hydroxylic groups using N,N‐dimethylacetamide/lithium chloride (DMAc/LiCl) as solvent with dicyclohexylcarbodiimide (DCC) and N,N‐dimethylaminopyridine (DMAP). Broom or cotton tocopherulate were prepared in the same conditions by using carboxylated fibers. Ester linkages were confirmed by using Fourier transformed infrared spectroscopy; biopolymers substitution degrees (DS) were determined by volumetric analysis. Antioxidant activity in inhibiting lipid peroxidation, in rat‐liver microsomal membranes, induced in vitro by two different sources of free radicals, 2,2′‐azobis (2‐amidinopropane) (AAPH) and tert‐butyl hydroperoxide (tert‐BOOH), was evaluated. Finally, biocompatibility of these biomaterials was also tested by controlling glutathione‐S‐transferase (GST) basal concentrations. Our results strongly suggested that the better derivatives were the ferulate ones. However, all obtained biomaterials, showing excellent antioxidant properties and biocompatibility, could be successfully applied in biomedical and in packaging areas. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009 Novel antioxidant biopolymers composed by broom or cotton fibers, and trans-ferulic acid, alpha-lipoic acid, and alpha-tocopherol, were prepared. The acids were directly linked to fibers microfibrils hydroxylic groups using N,N-dimethylacetamide/lithium chloride (DMAc/LiCl) as solvent with dicyclohexylcarbodiimide (DCC) and N,N-dimethylaminopyridine (DMAP). Broom or cotton tocopherulate were prepared in the same conditions by using carboxylated fibers. Ester linkages were confirmed by using Fourier transformed infrared spectroscopy; biopolymers substitution degrees (DS) were determined by volumetric analysis. Antioxidant activity in inhibiting lipid peroxidation, in rat-liver microsomal membranes, induced in vitro by two different sources of free radicals, 2,2'-azobis (2-amidinopropane) (AAPH) and tert-butyl hydroperoxide (tert-BOOH), was evaluated. Finally, biocompatibility of these biomaterials was also tested by controlling glutathione-S-transferase (GST) basal concentrations. Our results strongly suggested that the better derivatives were the ferulate ones. However, all obtained biomaterials, showing excellent antioxidant properties and biocompatibility, could be successfully applied in biomedical and in packaging areas. 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009 Novel antioxidant biopolymers composed by broom or cotton fibers, and trans-ferulic acid, -lipoic acid, and -tocopherol, were prepared. The acids were directly linked to fibers microfibrils hydroxylic groups using N,N-dimethylacetamide/lithium chloride (DMAc/LiCl) as solvent with dicyclohexylcarbodiimide (DCC) and N,N-dimethylaminopyridine (DMAP). Broom or cotton tocopherulate were prepared in the same conditions by using carboxylated fibers. Ester linkages were confirmed by using Fourier transformed infrared spectroscopy; biopolymers substitution degrees (DS) were determined by volumetric analysis. Antioxidant activity in inhibiting lipid peroxidation, in rat-liver microsomal membranes, induced in vitro by two different sources of free radicals, 2,2'-azobis (2-amidinopropane) (AAPH) and tert-butyl hydroperoxide (tert-BOOH), was evaluated. Finally, biocompatibility of these biomaterials was also tested by controlling glutathione-S-transferase (GST) basal concentrations. Our results strongly suggested that the better derivatives were the ferulate ones. However, all obtained biomaterials, showing excellent antioxidant properties and biocompatibility, could be successfully applied in biomedical and in packaging areas. [copy 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009 Abstract Novel antioxidant biopolymers composed by broom or cotton fibers, and trans ‐ferulic acid, α‐lipoic acid, and α‐tocopherol, were prepared. The acids were directly linked to fibers microfibrils hydroxylic groups using N , N ‐dimethylacetamide/lithium chloride (DMAc/LiCl) as solvent with dicyclohexylcarbodiimide (DCC) and N , N ‐dimethylaminopyridine (DMAP). Broom or cotton tocopherulate were prepared in the same conditions by using carboxylated fibers. Ester linkages were confirmed by using Fourier transformed infrared spectroscopy; biopolymers substitution degrees (DS) were determined by volumetric analysis. Antioxidant activity in inhibiting lipid peroxidation, in rat‐liver microsomal membranes, induced in vitro by two different sources of free radicals, 2,2′‐azobis (2‐amidinopropane) (AAPH) and tert ‐butyl hydroperoxide ( tert ‐BOOH), was evaluated. Finally, biocompatibility of these biomaterials was also tested by controlling glutathione‐S‐transferase (GST) basal concentrations. Our results strongly suggested that the better derivatives were the ferulate ones. However, all obtained biomaterials, showing excellent antioxidant properties and biocompatibility, could be successfully applied in biomedical and in packaging areas. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009 Novel antioxidant biopolymers composed by broom or cotton fibers, and trans-ferulic acid, α-lipoic acid, and α-tocopherol, were prepared. The acids were directly linked to fibers microfibrils hydroxylic groups using N,N-dimethylacetamide/lithium chloride (DMAc/LiCl) as solvent with dicyclohexylcarbodiimide (DCC) and N,N-dimethylaminopyridine (DMAP). Broom or cotton tocopherulate were prepared in the same conditions by using carboxylated fibers. Ester linkages were confirmed by using Fourier transformed infrared spectroscopy; biopolymers substitution degrees (DS) were determined by volumetric analysis. Antioxidant activity in inhibiting lipid peroxidation, in rat-liver microsomal membranes, induced in vitro by two different sources of free radicals, 2,2'-azobis (2-amidinopropane) (AAPH) and tert-butyl hydroperoxide (tert-BOOH), was evaluated. Finally, biocompatibility of these biomaterials was also tested by controlling glutathione-S-transferase (GST) basal concentrations. Our results strongly suggested that the better derivatives were the ferulate ones. However, all obtained biomaterials, showing excellent antioxidant properties and biocompatibility, could be successfully applied in biomedical and in packaging areas. |
| Author | Ferrarelli, Teresa Cassano, Roberta Nevio, Picci Cilea, Alessia Trombino, Sonia Muzzalupo, Rita Cione, Erika |
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| Keywords | Reaction inhibitor Biological properties Lipoic acid fibers antioxidants Plant fiber Lipids α-Tocopherol Additive Dicotyledones Natural fiber Angiospermae Reaction inhibition Biocompatibility Biomaterial biomaterials Cotton fiber Peroxidation infrared spectroscopy Microfibril Antioxidant Experimental study Ferulic acid biomedical and packaging areas Chemical modification Leguminosae Stabilizer agent Cytisus Preparation Cellulose derivatives Phenols Spermatophyta |
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| Snippet | Novel antioxidant biopolymers composed by broom or cotton fibers, and trans-ferulic acid, α-lipoic acid, and α-tocopherol, were prepared. The acids were... Novel antioxidant biopolymers composed by broom or cotton fibers, and trans‐ferulic acid, α‐lipoic acid, and α‐tocopherol, were prepared. The acids were... Abstract Novel antioxidant biopolymers composed by broom or cotton fibers, and trans ‐ferulic acid, α‐lipoic acid, and α‐tocopherol, were prepared. The acids... Novel antioxidant biopolymers composed by broom or cotton fibers, and trans-ferulic acid, alpha-lipoic acid, and alpha-tocopherol, were prepared. The acids... Novel antioxidant biopolymers composed by broom or cotton fibers, and trans-ferulic acid, -lipoic acid, and -tocopherol, were prepared. The acids were directly... |
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| SubjectTerms | antioxidants Applied sciences Biological and medical sciences biomaterials biomedical and packaging areas Exact sciences and technology fibers Fibers and threads Forms of application and semi-finished materials General pharmacology infrared spectroscopy Medical sciences Pharmaceutical technology. Pharmaceutical industry Pharmacology. Drug treatments Polymer industry, paints, wood Technology of polymers |
| Title | Synthesis and antioxidant activity evaluation of novel broom and cotton fibers derivatives |
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