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Enhanced absorption of hydroxysafflor yellow A using a self-double-emulsifying drug delivery system: in vitro and in vivo studies

Hydroxysafflor yellow A (HSYA), the main active ingredient of the safflower plant (Carthamus tinctorius L.), is a hydrophilic drug with low oral bioavailability. Water-in-oil-in-water (w/o/w) double emulsions may enhance the oral absorption of HSYA. In this study, we prepared a self-double-emulsifyi...

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Detalles Bibliográficos
Autores principales: Lv, Liang-Zhong, Tong, Chen-Qi, Lv, Qing, Tang, Xin-Jiang, Li, Li-Ming, Fang, Qing-Xia, Yu, Jia, Han, Min, Gao, Jian-Qing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3415323/
https://www.ncbi.nlm.nih.gov/pubmed/22888246
http://dx.doi.org/10.2147/IJN.S33398
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author Lv, Liang-Zhong
Tong, Chen-Qi
Lv, Qing
Tang, Xin-Jiang
Li, Li-Ming
Fang, Qing-Xia
Yu, Jia
Han, Min
Gao, Jian-Qing
author_facet Lv, Liang-Zhong
Tong, Chen-Qi
Lv, Qing
Tang, Xin-Jiang
Li, Li-Ming
Fang, Qing-Xia
Yu, Jia
Han, Min
Gao, Jian-Qing
author_sort Lv, Liang-Zhong
collection PubMed
description Hydroxysafflor yellow A (HSYA), the main active ingredient of the safflower plant (Carthamus tinctorius L.), is a hydrophilic drug with low oral bioavailability. Water-in-oil-in-water (w/o/w) double emulsions may enhance the oral absorption of HSYA. In this study, we prepared a self-double-emulsifying drug delivery system (SDEDDS) to improve the absorption of HSYA. SDEDDS consists of water in oil emulsions and hydrophilic surfactants that can self-emulsify into w/o/w double emulsions in the aqueous gastrointestinal environment. Confocal laser scanning micrographs showed that spherical droplets were uniformly distributed in the dispersion medium with narrow particle size distribution and could form fine w/o/w double emulsions upon dilution in dispersion medium with gentle stirring. The dispersed oil droplets contained small dispersed aqueous droplets consistent with the characteristics of double emulsions. Furthermore, in vitro cellular experiments were performed to study the mechanism of the absorption promoting effect of SDEDDS. The accumulation of rhodamine-123 in Caco-2 cells was used to evaluate the efflux transport of p-glycoprotein inhibitor. Histopathologic studies on the rat intestine showed that SDEDDS can cause mucosal damage to a certain degree of toxicity, however this was not serious. These results suggest that SDEDDS can greatly improve the oral absorption of HSYA. Given the toxicity demonstrated to the small intestine, the formulation prescription should be improved to enhance security in the future.
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spelling pubmed-34153232012-08-10 Enhanced absorption of hydroxysafflor yellow A using a self-double-emulsifying drug delivery system: in vitro and in vivo studies Lv, Liang-Zhong Tong, Chen-Qi Lv, Qing Tang, Xin-Jiang Li, Li-Ming Fang, Qing-Xia Yu, Jia Han, Min Gao, Jian-Qing Int J Nanomedicine Original Research Hydroxysafflor yellow A (HSYA), the main active ingredient of the safflower plant (Carthamus tinctorius L.), is a hydrophilic drug with low oral bioavailability. Water-in-oil-in-water (w/o/w) double emulsions may enhance the oral absorption of HSYA. In this study, we prepared a self-double-emulsifying drug delivery system (SDEDDS) to improve the absorption of HSYA. SDEDDS consists of water in oil emulsions and hydrophilic surfactants that can self-emulsify into w/o/w double emulsions in the aqueous gastrointestinal environment. Confocal laser scanning micrographs showed that spherical droplets were uniformly distributed in the dispersion medium with narrow particle size distribution and could form fine w/o/w double emulsions upon dilution in dispersion medium with gentle stirring. The dispersed oil droplets contained small dispersed aqueous droplets consistent with the characteristics of double emulsions. Furthermore, in vitro cellular experiments were performed to study the mechanism of the absorption promoting effect of SDEDDS. The accumulation of rhodamine-123 in Caco-2 cells was used to evaluate the efflux transport of p-glycoprotein inhibitor. Histopathologic studies on the rat intestine showed that SDEDDS can cause mucosal damage to a certain degree of toxicity, however this was not serious. These results suggest that SDEDDS can greatly improve the oral absorption of HSYA. Given the toxicity demonstrated to the small intestine, the formulation prescription should be improved to enhance security in the future. Dove Medical Press 2012 2012-07-30 /pmc/articles/PMC3415323/ /pubmed/22888246 http://dx.doi.org/10.2147/IJN.S33398 Text en © 2012 Lv et al, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Original Research
Lv, Liang-Zhong
Tong, Chen-Qi
Lv, Qing
Tang, Xin-Jiang
Li, Li-Ming
Fang, Qing-Xia
Yu, Jia
Han, Min
Gao, Jian-Qing
Enhanced absorption of hydroxysafflor yellow A using a self-double-emulsifying drug delivery system: in vitro and in vivo studies
title Enhanced absorption of hydroxysafflor yellow A using a self-double-emulsifying drug delivery system: in vitro and in vivo studies
title_full Enhanced absorption of hydroxysafflor yellow A using a self-double-emulsifying drug delivery system: in vitro and in vivo studies
title_fullStr Enhanced absorption of hydroxysafflor yellow A using a self-double-emulsifying drug delivery system: in vitro and in vivo studies
title_full_unstemmed Enhanced absorption of hydroxysafflor yellow A using a self-double-emulsifying drug delivery system: in vitro and in vivo studies
title_short Enhanced absorption of hydroxysafflor yellow A using a self-double-emulsifying drug delivery system: in vitro and in vivo studies
title_sort enhanced absorption of hydroxysafflor yellow a using a self-double-emulsifying drug delivery system: in vitro and in vivo studies
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3415323/
https://www.ncbi.nlm.nih.gov/pubmed/22888246
http://dx.doi.org/10.2147/IJN.S33398
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