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Unroasted Green Coffee Extract-Loaded Solid Lipid Nanoparticles for Enhancing Intestinal Permeation
[Image: see text] Green coffee bean extract (GCBE) provides diversified health benefits. However, its reported low bioavailability impeded its utilization in various applications. In this study, GCBE-loaded solid lipid nanoparticles (SLNs) were prepared to improve the bioavailability through enhance...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10268626/ https://www.ncbi.nlm.nih.gov/pubmed/37332788 http://dx.doi.org/10.1021/acsomega.2c06629 |
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author | Moussa, Yomna A. Teaima, Mahmoud H. Attia, Dalia Elmazar, Mohey M. El-Nabarawi, Mohamed A. |
author_facet | Moussa, Yomna A. Teaima, Mahmoud H. Attia, Dalia Elmazar, Mohey M. El-Nabarawi, Mohamed A. |
author_sort | Moussa, Yomna A. |
collection | PubMed |
description | [Image: see text] Green coffee bean extract (GCBE) provides diversified health benefits. However, its reported low bioavailability impeded its utilization in various applications. In this study, GCBE-loaded solid lipid nanoparticles (SLNs) were prepared to improve the bioavailability through enhanced intestinal absorption of GCBE. During the preparation of promising GCBE-loaded SLNs, the lipid concentration, surfactant concentration, and co-surfactant amount are crucial that were optimized using the Box–Behnken design, while particle size, polydispersity index (PDI), ζ-potential, entrapment efficiency, and cumulative drug release were the measured responses. GCBE-SLNs were successfully developed by a high shear homogenization technique using geleol as a solid lipid, tween 80 as a surfactant, and propylene glycol as Co-SAA. The optimized SLNs contained 5.8% geleol, 5.9% tween 80, and 80.4 mg PG resulting in a small particle size of 235.7 ± 12.5 nm, reasonably acceptable PDI of 0.417 ± 0.023, and ζ-potential of −15 ± 0.14 mV, with a high entrapment efficiency of 58.3 ± 0.85% and cumulative release of 7575 ± 0.78%. Furthermore, the performance of the optimized GCBE-SLN was evaluated using an ex vivo everted sac model where the intestinal permeation of GCBE was improved due to nanoencapsulation using SLN. Consequently, the results enlightened the auspicious potential of exploiting oral GCBE-SLNs for boosting intestinal absorption of chlorogenic acid. |
format | Online Article Text |
id | pubmed-10268626 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-102686262023-06-16 Unroasted Green Coffee Extract-Loaded Solid Lipid Nanoparticles for Enhancing Intestinal Permeation Moussa, Yomna A. Teaima, Mahmoud H. Attia, Dalia Elmazar, Mohey M. El-Nabarawi, Mohamed A. ACS Omega [Image: see text] Green coffee bean extract (GCBE) provides diversified health benefits. However, its reported low bioavailability impeded its utilization in various applications. In this study, GCBE-loaded solid lipid nanoparticles (SLNs) were prepared to improve the bioavailability through enhanced intestinal absorption of GCBE. During the preparation of promising GCBE-loaded SLNs, the lipid concentration, surfactant concentration, and co-surfactant amount are crucial that were optimized using the Box–Behnken design, while particle size, polydispersity index (PDI), ζ-potential, entrapment efficiency, and cumulative drug release were the measured responses. GCBE-SLNs were successfully developed by a high shear homogenization technique using geleol as a solid lipid, tween 80 as a surfactant, and propylene glycol as Co-SAA. The optimized SLNs contained 5.8% geleol, 5.9% tween 80, and 80.4 mg PG resulting in a small particle size of 235.7 ± 12.5 nm, reasonably acceptable PDI of 0.417 ± 0.023, and ζ-potential of −15 ± 0.14 mV, with a high entrapment efficiency of 58.3 ± 0.85% and cumulative release of 7575 ± 0.78%. Furthermore, the performance of the optimized GCBE-SLN was evaluated using an ex vivo everted sac model where the intestinal permeation of GCBE was improved due to nanoencapsulation using SLN. Consequently, the results enlightened the auspicious potential of exploiting oral GCBE-SLNs for boosting intestinal absorption of chlorogenic acid. American Chemical Society 2023-06-01 /pmc/articles/PMC10268626/ /pubmed/37332788 http://dx.doi.org/10.1021/acsomega.2c06629 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Moussa, Yomna A. Teaima, Mahmoud H. Attia, Dalia Elmazar, Mohey M. El-Nabarawi, Mohamed A. Unroasted Green Coffee Extract-Loaded Solid Lipid Nanoparticles for Enhancing Intestinal Permeation |
title | Unroasted Green
Coffee Extract-Loaded Solid Lipid
Nanoparticles for Enhancing Intestinal Permeation |
title_full | Unroasted Green
Coffee Extract-Loaded Solid Lipid
Nanoparticles for Enhancing Intestinal Permeation |
title_fullStr | Unroasted Green
Coffee Extract-Loaded Solid Lipid
Nanoparticles for Enhancing Intestinal Permeation |
title_full_unstemmed | Unroasted Green
Coffee Extract-Loaded Solid Lipid
Nanoparticles for Enhancing Intestinal Permeation |
title_short | Unroasted Green
Coffee Extract-Loaded Solid Lipid
Nanoparticles for Enhancing Intestinal Permeation |
title_sort | unroasted green
coffee extract-loaded solid lipid
nanoparticles for enhancing intestinal permeation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10268626/ https://www.ncbi.nlm.nih.gov/pubmed/37332788 http://dx.doi.org/10.1021/acsomega.2c06629 |
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