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Enhancement of Curcumin Bioavailability Using Nanocellulose Reinforced Chitosan Hydrogel

A unique biodegradable, superporous, swellable and pH sensitive nanocellulose reinforced chitosan hydrogel with dynamic mechanical properties was prepared for oral administration of curcumin. Curcumin, a less water-soluble drug was used due to the fact that the fast swellable, superporous hydrogel c...

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Autores principales: Udeni Gunathilake, Thennakoon M. Sampath, Ching, Yern Chee, Chuah, Cheng Hock
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6431856/
https://www.ncbi.nlm.nih.gov/pubmed/30970742
http://dx.doi.org/10.3390/polym9020064
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author Udeni Gunathilake, Thennakoon M. Sampath
Ching, Yern Chee
Chuah, Cheng Hock
author_facet Udeni Gunathilake, Thennakoon M. Sampath
Ching, Yern Chee
Chuah, Cheng Hock
author_sort Udeni Gunathilake, Thennakoon M. Sampath
collection PubMed
description A unique biodegradable, superporous, swellable and pH sensitive nanocellulose reinforced chitosan hydrogel with dynamic mechanical properties was prepared for oral administration of curcumin. Curcumin, a less water-soluble drug was used due to the fact that the fast swellable, superporous hydrogel could release a water-insoluble drug to a great extent. CO(2) gas foaming was used to fabricate hydrogel as it eradicates using organic solvents. Field emission scanning electron microscope images revealed that the pore size significantly increased with the formation of widely interconnected porous structure in gas foamed hydrogels. The maximum compression of pure chitosan hydrogel was 25.9 ± 1 kPa and it increased to 38.4 ± 1 kPa with the introduction of 0.5% cellulose nanocrystals. In vitro degradation of hydrogels was found dependent on the swelling ratio and the amount of CNC of the hydrogel. All the hydrogels showed maximum swelling ratios greater than 300%. The 0.5% CNC-chitosan hydrogel showed the highest swelling ratio of 438% ± 11%. FTIR spectrum indicated that there is no interaction between drug and ingredients present in hydrogels. The drug release occurred in non-Fickian (anomalous) manner in simulated gastric medium. The drug release profiles of hydrogels are consistent with the data obtained from the swelling studies. After gas foaming of the hydrogel, the drug loading efficiency increased from 41% ± 2.4% to 50% ± 2.0% and release increased from 0.74 to 1.06 mg/L. The drug release data showed good fitting to Ritger-Peppas model. Moreover, the results revealed that the drug maintained its chemical activity after in vitro release. According to the results of this study, CNC reinforced chitosan hydrogel can be suggested to improve the bioavailability of curcumin for the absorption from stomach and upper intestinal tract.
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spelling pubmed-64318562019-04-02 Enhancement of Curcumin Bioavailability Using Nanocellulose Reinforced Chitosan Hydrogel Udeni Gunathilake, Thennakoon M. Sampath Ching, Yern Chee Chuah, Cheng Hock Polymers (Basel) Article A unique biodegradable, superporous, swellable and pH sensitive nanocellulose reinforced chitosan hydrogel with dynamic mechanical properties was prepared for oral administration of curcumin. Curcumin, a less water-soluble drug was used due to the fact that the fast swellable, superporous hydrogel could release a water-insoluble drug to a great extent. CO(2) gas foaming was used to fabricate hydrogel as it eradicates using organic solvents. Field emission scanning electron microscope images revealed that the pore size significantly increased with the formation of widely interconnected porous structure in gas foamed hydrogels. The maximum compression of pure chitosan hydrogel was 25.9 ± 1 kPa and it increased to 38.4 ± 1 kPa with the introduction of 0.5% cellulose nanocrystals. In vitro degradation of hydrogels was found dependent on the swelling ratio and the amount of CNC of the hydrogel. All the hydrogels showed maximum swelling ratios greater than 300%. The 0.5% CNC-chitosan hydrogel showed the highest swelling ratio of 438% ± 11%. FTIR spectrum indicated that there is no interaction between drug and ingredients present in hydrogels. The drug release occurred in non-Fickian (anomalous) manner in simulated gastric medium. The drug release profiles of hydrogels are consistent with the data obtained from the swelling studies. After gas foaming of the hydrogel, the drug loading efficiency increased from 41% ± 2.4% to 50% ± 2.0% and release increased from 0.74 to 1.06 mg/L. The drug release data showed good fitting to Ritger-Peppas model. Moreover, the results revealed that the drug maintained its chemical activity after in vitro release. According to the results of this study, CNC reinforced chitosan hydrogel can be suggested to improve the bioavailability of curcumin for the absorption from stomach and upper intestinal tract. MDPI 2017-02-15 /pmc/articles/PMC6431856/ /pubmed/30970742 http://dx.doi.org/10.3390/polym9020064 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Udeni Gunathilake, Thennakoon M. Sampath
Ching, Yern Chee
Chuah, Cheng Hock
Enhancement of Curcumin Bioavailability Using Nanocellulose Reinforced Chitosan Hydrogel
title Enhancement of Curcumin Bioavailability Using Nanocellulose Reinforced Chitosan Hydrogel
title_full Enhancement of Curcumin Bioavailability Using Nanocellulose Reinforced Chitosan Hydrogel
title_fullStr Enhancement of Curcumin Bioavailability Using Nanocellulose Reinforced Chitosan Hydrogel
title_full_unstemmed Enhancement of Curcumin Bioavailability Using Nanocellulose Reinforced Chitosan Hydrogel
title_short Enhancement of Curcumin Bioavailability Using Nanocellulose Reinforced Chitosan Hydrogel
title_sort enhancement of curcumin bioavailability using nanocellulose reinforced chitosan hydrogel
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6431856/
https://www.ncbi.nlm.nih.gov/pubmed/30970742
http://dx.doi.org/10.3390/polym9020064
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