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Microspheres as carriers for lipase inhibitory substances to reduce dietary triglyceride absorption in mice

The present study intends to use microspheres as a delivery system of chlorogenic acid (CGA) to investigate the influences of CGA microspheres on dietary fat absorption and fecal triglyceride excretion in a mice model. Microspheres have an average particle size of about 53.3 μm. Results indicated th...

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Detalles Bibliográficos
Autores principales: Wu, Shiuan-Huei, Sun, Nan-Nong, Chau, Chi-Fai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taiwan Food and Drug Administration 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9345438/
https://www.ncbi.nlm.nih.gov/pubmed/28911395
http://dx.doi.org/10.1016/j.jfda.2015.08.002
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author Wu, Shiuan-Huei
Sun, Nan-Nong
Chau, Chi-Fai
author_facet Wu, Shiuan-Huei
Sun, Nan-Nong
Chau, Chi-Fai
author_sort Wu, Shiuan-Huei
collection PubMed
description The present study intends to use microspheres as a delivery system of chlorogenic acid (CGA) to investigate the influences of CGA microspheres on dietary fat absorption and fecal triglyceride excretion in a mice model. Microspheres have an average particle size of about 53.3 μm. Results indicated that the microspheres were capable of gradually releasing the preloaded CGA into the surrounding medium. Their bioadhesive property might help prolong the gastrointestinal transit time in mice, and render a better mixing and contact between CGA and triglyceride. Consumption of CGA microspheres resulted in a significantly higher level of fecal triglyceride (119–144%) as compared with the corresponding control groups. A microsphere would be a desirable vehicle for CGA to improve its efficacy along the intestine.
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spelling pubmed-93454382022-08-09 Microspheres as carriers for lipase inhibitory substances to reduce dietary triglyceride absorption in mice Wu, Shiuan-Huei Sun, Nan-Nong Chau, Chi-Fai J Food Drug Anal Original Article The present study intends to use microspheres as a delivery system of chlorogenic acid (CGA) to investigate the influences of CGA microspheres on dietary fat absorption and fecal triglyceride excretion in a mice model. Microspheres have an average particle size of about 53.3 μm. Results indicated that the microspheres were capable of gradually releasing the preloaded CGA into the surrounding medium. Their bioadhesive property might help prolong the gastrointestinal transit time in mice, and render a better mixing and contact between CGA and triglyceride. Consumption of CGA microspheres resulted in a significantly higher level of fecal triglyceride (119–144%) as compared with the corresponding control groups. A microsphere would be a desirable vehicle for CGA to improve its efficacy along the intestine. Taiwan Food and Drug Administration 2015-10-16 /pmc/articles/PMC9345438/ /pubmed/28911395 http://dx.doi.org/10.1016/j.jfda.2015.08.002 Text en © 2016 Taiwan Food and Drug Administration https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC-BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ).
spellingShingle Original Article
Wu, Shiuan-Huei
Sun, Nan-Nong
Chau, Chi-Fai
Microspheres as carriers for lipase inhibitory substances to reduce dietary triglyceride absorption in mice
title Microspheres as carriers for lipase inhibitory substances to reduce dietary triglyceride absorption in mice
title_full Microspheres as carriers for lipase inhibitory substances to reduce dietary triglyceride absorption in mice
title_fullStr Microspheres as carriers for lipase inhibitory substances to reduce dietary triglyceride absorption in mice
title_full_unstemmed Microspheres as carriers for lipase inhibitory substances to reduce dietary triglyceride absorption in mice
title_short Microspheres as carriers for lipase inhibitory substances to reduce dietary triglyceride absorption in mice
title_sort microspheres as carriers for lipase inhibitory substances to reduce dietary triglyceride absorption in mice
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9345438/
https://www.ncbi.nlm.nih.gov/pubmed/28911395
http://dx.doi.org/10.1016/j.jfda.2015.08.002
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