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The Formulation of Curcumin: 2-Hydroxypropyl-β-cyclodextrin Complex with Smart Hydrogel for Prolonged Release of Curcumin
Curcumin comes from the plant species Curcuma longa and shows numerous pharmacological activities. There are numerous curcumin formulations with gels or cyclodextrins in order to increase its solubility and bioavailability. This paper presents the formulation of complex of curcumin with 2-hydroxypro...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9967663/ https://www.ncbi.nlm.nih.gov/pubmed/36839703 http://dx.doi.org/10.3390/pharmaceutics15020382 |
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author | Nikolić, Ljubiša Urošević, Maja Nikolić, Vesna Gajić, Ivana Dinić, Ana Miljković, Vojkan Rakić, Srđan Đokić, Sanja Kesić, Jelena Ilić-Stojanović, Snežana Nikolić, Goran |
author_facet | Nikolić, Ljubiša Urošević, Maja Nikolić, Vesna Gajić, Ivana Dinić, Ana Miljković, Vojkan Rakić, Srđan Đokić, Sanja Kesić, Jelena Ilić-Stojanović, Snežana Nikolić, Goran |
author_sort | Nikolić, Ljubiša |
collection | PubMed |
description | Curcumin comes from the plant species Curcuma longa and shows numerous pharmacological activities. There are numerous curcumin formulations with gels or cyclodextrins in order to increase its solubility and bioavailability. This paper presents the formulation of complex of curcumin with 2-hydroxypropyl-β-cyclodextrin in a thermosensitive hydrogel, based on N-isopropylmethacrylamide and N-isopropylacrylamide with ethylene glycol dimethacrylate as a crosslinker. The product was characterized by chemical methods and also by FTIR, HPLC, DSC, SEM, XRD. The results show that synthesis was successfully done. With an increase in the quantity of crosslinker in the hydrogels, the starting release and the release rate of curcumin from the formulation of the complex with hydrogels decreases. The release rate of curcumin from the gel complex formulation is constant over time. It is possible to design a formulation that will release curcumin for more than 60 days. In order to determine the mechanism and kinetics of curcumin release, various mathematical models were applied by using the DDSolver package for Microsoft Excel application. The Korsmeyer-Peppas model best describes the release of curcumin from the gel formulation of the complex, while the values for the diffusion exponent (0.063–0.074) shows that mechanism of the release rate is based on diffusion. |
format | Online Article Text |
id | pubmed-9967663 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-99676632023-02-27 The Formulation of Curcumin: 2-Hydroxypropyl-β-cyclodextrin Complex with Smart Hydrogel for Prolonged Release of Curcumin Nikolić, Ljubiša Urošević, Maja Nikolić, Vesna Gajić, Ivana Dinić, Ana Miljković, Vojkan Rakić, Srđan Đokić, Sanja Kesić, Jelena Ilić-Stojanović, Snežana Nikolić, Goran Pharmaceutics Article Curcumin comes from the plant species Curcuma longa and shows numerous pharmacological activities. There are numerous curcumin formulations with gels or cyclodextrins in order to increase its solubility and bioavailability. This paper presents the formulation of complex of curcumin with 2-hydroxypropyl-β-cyclodextrin in a thermosensitive hydrogel, based on N-isopropylmethacrylamide and N-isopropylacrylamide with ethylene glycol dimethacrylate as a crosslinker. The product was characterized by chemical methods and also by FTIR, HPLC, DSC, SEM, XRD. The results show that synthesis was successfully done. With an increase in the quantity of crosslinker in the hydrogels, the starting release and the release rate of curcumin from the formulation of the complex with hydrogels decreases. The release rate of curcumin from the gel complex formulation is constant over time. It is possible to design a formulation that will release curcumin for more than 60 days. In order to determine the mechanism and kinetics of curcumin release, various mathematical models were applied by using the DDSolver package for Microsoft Excel application. The Korsmeyer-Peppas model best describes the release of curcumin from the gel formulation of the complex, while the values for the diffusion exponent (0.063–0.074) shows that mechanism of the release rate is based on diffusion. MDPI 2023-01-22 /pmc/articles/PMC9967663/ /pubmed/36839703 http://dx.doi.org/10.3390/pharmaceutics15020382 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Nikolić, Ljubiša Urošević, Maja Nikolić, Vesna Gajić, Ivana Dinić, Ana Miljković, Vojkan Rakić, Srđan Đokić, Sanja Kesić, Jelena Ilić-Stojanović, Snežana Nikolić, Goran The Formulation of Curcumin: 2-Hydroxypropyl-β-cyclodextrin Complex with Smart Hydrogel for Prolonged Release of Curcumin |
title | The Formulation of Curcumin: 2-Hydroxypropyl-β-cyclodextrin Complex with Smart Hydrogel for Prolonged Release of Curcumin |
title_full | The Formulation of Curcumin: 2-Hydroxypropyl-β-cyclodextrin Complex with Smart Hydrogel for Prolonged Release of Curcumin |
title_fullStr | The Formulation of Curcumin: 2-Hydroxypropyl-β-cyclodextrin Complex with Smart Hydrogel for Prolonged Release of Curcumin |
title_full_unstemmed | The Formulation of Curcumin: 2-Hydroxypropyl-β-cyclodextrin Complex with Smart Hydrogel for Prolonged Release of Curcumin |
title_short | The Formulation of Curcumin: 2-Hydroxypropyl-β-cyclodextrin Complex with Smart Hydrogel for Prolonged Release of Curcumin |
title_sort | formulation of curcumin: 2-hydroxypropyl-β-cyclodextrin complex with smart hydrogel for prolonged release of curcumin |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9967663/ https://www.ncbi.nlm.nih.gov/pubmed/36839703 http://dx.doi.org/10.3390/pharmaceutics15020382 |
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