A supersaturating delivery system of silibinin exhibiting high payload achieved by amorphous nano-complexation with chitosan

The therapeutic potentials of silibinin – a phytochemical isolated from milk thistle plants – have not been fully realized due to its poor oral bioavailability caused by the low aqueous solubility. Existing solubility enhancement strategies of silibinin by nanonization were limited by their low payl...

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Main Authors: Nguyen, Minh-Hiep, Yu, Hong, Dong, Bingxue, Hadinoto, Kunn
Other Authors: School of Chemical and Biomedical Engineering
Format: Article
Language:English
Published: 2016
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Online Access:https://hdl.handle.net/10356/84608
http://hdl.handle.net/10220/41896
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-846082023-12-29T06:49:31Z A supersaturating delivery system of silibinin exhibiting high payload achieved by amorphous nano-complexation with chitosan Nguyen, Minh-Hiep Yu, Hong Dong, Bingxue Hadinoto, Kunn School of Chemical and Biomedical Engineering Silymarin Silybin The therapeutic potentials of silibinin – a phytochemical isolated from milk thistle plants – have not been fully realized due to its poor oral bioavailability caused by the low aqueous solubility. Existing solubility enhancement strategies of silibinin by nanonization were limited by their low payload. Herein we developed a supersaturating delivery system of silibinin exhibiting a high payload (≈ 76%) in the form of amorphous silibinin–chitosan nanoparticle complex (or silibinin nanoplex in short) prepared by self-assembly drug-polysaccharide complexation. The effects of (1) pH and (2) charge ratio of chitosan to silibinin on the nanoplex's physical characteristics (i.e. size, zeta potential, and payload) and preparation efficiency (i.e. silibinin utilization, overall yield) were investigated. The formation of nanoplex (≈ 240 nm) was feasible only in a narrow pH range (5.1–5.8) and favored charge ratio below unity. At the optimal condition (pH 5.8 and charge ratio of 0.30), the nanoplex preparation exhibited 87% silibinin utilization rate and 63% yield signifying its high efficiency. The amorphous state and colloidal stabilities of the nanoplex during storage, and prolonged supersaturation generation (3 h) at more than 10 × of the saturation solubility were successfully demonstrated. Accepted version 2016-12-20T09:07:06Z 2019-12-06T15:48:15Z 2016-12-20T09:07:06Z 2019-12-06T15:48:15Z 2016 Journal Article Nguyen, M. -H., Yu, H., Dong, B., & Hadinoto, K. (2016). A supersaturating delivery system of silibinin exhibiting high payload achieved by amorphous nano-complexation with chitosan. European Journal of Pharmaceutical Sciences, 89, 163-171. 0928-0987 https://hdl.handle.net/10356/84608 http://hdl.handle.net/10220/41896 10.1016/j.ejps.2016.04.036 en European Journal of Pharmaceutical Sciences © 2016 Elsevier B. V. This is the author created version of a work that has been peer reviewed and accepted for publication by European Journal of Pharmaceutical Sciences, Elsevier. It incorporates referee’s comments but changes resulting from the publishing process, such as copyediting, structural formatting, may not be reflected in this document. The published version is available at: [http://dx.doi.org/10.1016/j.ejps.2016.04.036]. 35 p. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Silymarin
Silybin
spellingShingle Silymarin
Silybin
Nguyen, Minh-Hiep
Yu, Hong
Dong, Bingxue
Hadinoto, Kunn
A supersaturating delivery system of silibinin exhibiting high payload achieved by amorphous nano-complexation with chitosan
description The therapeutic potentials of silibinin – a phytochemical isolated from milk thistle plants – have not been fully realized due to its poor oral bioavailability caused by the low aqueous solubility. Existing solubility enhancement strategies of silibinin by nanonization were limited by their low payload. Herein we developed a supersaturating delivery system of silibinin exhibiting a high payload (≈ 76%) in the form of amorphous silibinin–chitosan nanoparticle complex (or silibinin nanoplex in short) prepared by self-assembly drug-polysaccharide complexation. The effects of (1) pH and (2) charge ratio of chitosan to silibinin on the nanoplex's physical characteristics (i.e. size, zeta potential, and payload) and preparation efficiency (i.e. silibinin utilization, overall yield) were investigated. The formation of nanoplex (≈ 240 nm) was feasible only in a narrow pH range (5.1–5.8) and favored charge ratio below unity. At the optimal condition (pH 5.8 and charge ratio of 0.30), the nanoplex preparation exhibited 87% silibinin utilization rate and 63% yield signifying its high efficiency. The amorphous state and colloidal stabilities of the nanoplex during storage, and prolonged supersaturation generation (3 h) at more than 10 × of the saturation solubility were successfully demonstrated.
author2 School of Chemical and Biomedical Engineering
author_facet School of Chemical and Biomedical Engineering
Nguyen, Minh-Hiep
Yu, Hong
Dong, Bingxue
Hadinoto, Kunn
format Article
author Nguyen, Minh-Hiep
Yu, Hong
Dong, Bingxue
Hadinoto, Kunn
author_sort Nguyen, Minh-Hiep
title A supersaturating delivery system of silibinin exhibiting high payload achieved by amorphous nano-complexation with chitosan
title_short A supersaturating delivery system of silibinin exhibiting high payload achieved by amorphous nano-complexation with chitosan
title_full A supersaturating delivery system of silibinin exhibiting high payload achieved by amorphous nano-complexation with chitosan
title_fullStr A supersaturating delivery system of silibinin exhibiting high payload achieved by amorphous nano-complexation with chitosan
title_full_unstemmed A supersaturating delivery system of silibinin exhibiting high payload achieved by amorphous nano-complexation with chitosan
title_sort supersaturating delivery system of silibinin exhibiting high payload achieved by amorphous nano-complexation with chitosan
publishDate 2016
url https://hdl.handle.net/10356/84608
http://hdl.handle.net/10220/41896
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