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Preparation and Evaluation of Resveratrol-Loaded Composite Nanoparticles Using a Supercritical Fluid Technology for Enhanced Oral and Skin Delivery

We created composite nanoparticles containing hydrophilic additives using a supercritical antisolvent (SAS) process to increase the solubility and dissolution properties of trans-resveratrol for application in oral and skin delivery. Physicochemical properties of trans-resveratrol-loaded composite n...

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Autores principales: Ha, Eun-Sol, Sim, Woo-Yong, Lee, Seon-Kwang, Jeong, Ji-Su, Kim, Jeong-Soo, Baek, In-hwan, Choi, Du Hyung, Park, Heejun, Hwang, Sung-Joo, Kim, Min-Soo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6912748/
https://www.ncbi.nlm.nih.gov/pubmed/31739617
http://dx.doi.org/10.3390/antiox8110554
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author Ha, Eun-Sol
Sim, Woo-Yong
Lee, Seon-Kwang
Jeong, Ji-Su
Kim, Jeong-Soo
Baek, In-hwan
Choi, Du Hyung
Park, Heejun
Hwang, Sung-Joo
Kim, Min-Soo
author_facet Ha, Eun-Sol
Sim, Woo-Yong
Lee, Seon-Kwang
Jeong, Ji-Su
Kim, Jeong-Soo
Baek, In-hwan
Choi, Du Hyung
Park, Heejun
Hwang, Sung-Joo
Kim, Min-Soo
author_sort Ha, Eun-Sol
collection PubMed
description We created composite nanoparticles containing hydrophilic additives using a supercritical antisolvent (SAS) process to increase the solubility and dissolution properties of trans-resveratrol for application in oral and skin delivery. Physicochemical properties of trans-resveratrol-loaded composite nanoparticles were characterized. In addition, an in vitro dissolution–permeation study, an in vivo pharmacokinetic study in rats, and an ex vivo skin permeation study in rats were performed. The mean particle size of all the composite nanoparticles produced was less than 300 nm. Compared to micronized trans-resveratrol, the trans-resveratrol/hydroxylpropylmethyl cellulose (HPMC)/poloxamer 407 (1:4:1) nanoparticles with the highest flux (0.792 μg/min/cm(2)) exhibited rapid absorption and showed significantly higher exposure 4 h after oral administration. Good correlations were observed between in vitro flux and in vivo pharmacokinetic data. The increased solubility and flux of trans-resveratrol generated by the HPMC/surfactant nanoparticles increased the driving force on the gastrointestinal epithelial membrane and rat skin, resulting in enhanced oral and skin delivery of trans-resveratrol. HPMC/surfactant nanoparticles produced by an SAS process are, thus, a promising formulation method for trans-resveratrol for healthcare products (owing to their enhanced absorption via oral administration) and for skin application with cosmetic products.
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spelling pubmed-69127482020-01-02 Preparation and Evaluation of Resveratrol-Loaded Composite Nanoparticles Using a Supercritical Fluid Technology for Enhanced Oral and Skin Delivery Ha, Eun-Sol Sim, Woo-Yong Lee, Seon-Kwang Jeong, Ji-Su Kim, Jeong-Soo Baek, In-hwan Choi, Du Hyung Park, Heejun Hwang, Sung-Joo Kim, Min-Soo Antioxidants (Basel) Article We created composite nanoparticles containing hydrophilic additives using a supercritical antisolvent (SAS) process to increase the solubility and dissolution properties of trans-resveratrol for application in oral and skin delivery. Physicochemical properties of trans-resveratrol-loaded composite nanoparticles were characterized. In addition, an in vitro dissolution–permeation study, an in vivo pharmacokinetic study in rats, and an ex vivo skin permeation study in rats were performed. The mean particle size of all the composite nanoparticles produced was less than 300 nm. Compared to micronized trans-resveratrol, the trans-resveratrol/hydroxylpropylmethyl cellulose (HPMC)/poloxamer 407 (1:4:1) nanoparticles with the highest flux (0.792 μg/min/cm(2)) exhibited rapid absorption and showed significantly higher exposure 4 h after oral administration. Good correlations were observed between in vitro flux and in vivo pharmacokinetic data. The increased solubility and flux of trans-resveratrol generated by the HPMC/surfactant nanoparticles increased the driving force on the gastrointestinal epithelial membrane and rat skin, resulting in enhanced oral and skin delivery of trans-resveratrol. HPMC/surfactant nanoparticles produced by an SAS process are, thus, a promising formulation method for trans-resveratrol for healthcare products (owing to their enhanced absorption via oral administration) and for skin application with cosmetic products. MDPI 2019-11-14 /pmc/articles/PMC6912748/ /pubmed/31739617 http://dx.doi.org/10.3390/antiox8110554 Text en © 2019 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
Ha, Eun-Sol
Sim, Woo-Yong
Lee, Seon-Kwang
Jeong, Ji-Su
Kim, Jeong-Soo
Baek, In-hwan
Choi, Du Hyung
Park, Heejun
Hwang, Sung-Joo
Kim, Min-Soo
Preparation and Evaluation of Resveratrol-Loaded Composite Nanoparticles Using a Supercritical Fluid Technology for Enhanced Oral and Skin Delivery
title Preparation and Evaluation of Resveratrol-Loaded Composite Nanoparticles Using a Supercritical Fluid Technology for Enhanced Oral and Skin Delivery
title_full Preparation and Evaluation of Resveratrol-Loaded Composite Nanoparticles Using a Supercritical Fluid Technology for Enhanced Oral and Skin Delivery
title_fullStr Preparation and Evaluation of Resveratrol-Loaded Composite Nanoparticles Using a Supercritical Fluid Technology for Enhanced Oral and Skin Delivery
title_full_unstemmed Preparation and Evaluation of Resveratrol-Loaded Composite Nanoparticles Using a Supercritical Fluid Technology for Enhanced Oral and Skin Delivery
title_short Preparation and Evaluation of Resveratrol-Loaded Composite Nanoparticles Using a Supercritical Fluid Technology for Enhanced Oral and Skin Delivery
title_sort preparation and evaluation of resveratrol-loaded composite nanoparticles using a supercritical fluid technology for enhanced oral and skin delivery
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6912748/
https://www.ncbi.nlm.nih.gov/pubmed/31739617
http://dx.doi.org/10.3390/antiox8110554
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