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Hydrophilic and Hydrophobic Mesoporous Silica Derived from Rice Husk Ash as a Potential Drug Carrier

This work describes the preparation of mesoporous silica by the green reaction of rice husk ash (RHA) with glycerol, followed by the modification and the potential use as a drug carrier. The reaction was carried out at 215 °C for 2 h. The solution was further hydrolyzed with deionized water and aged...

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Autores principales: Suttiruengwong, Supakij, Pivsa-Art, Sommai, Chareonpanich, Metta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6073255/
https://www.ncbi.nlm.nih.gov/pubmed/29976886
http://dx.doi.org/10.3390/ma11071142
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author Suttiruengwong, Supakij
Pivsa-Art, Sommai
Chareonpanich, Metta
author_facet Suttiruengwong, Supakij
Pivsa-Art, Sommai
Chareonpanich, Metta
author_sort Suttiruengwong, Supakij
collection PubMed
description This work describes the preparation of mesoporous silica by the green reaction of rice husk ash (RHA) with glycerol, followed by the modification and the potential use as a drug carrier. The reaction was carried out at 215 °C for 2 h. The solution was further hydrolyzed with deionized water and aged for various times (24, 48, 120, 360, 528 and 672 h) before calcinations at 500 °C for 24 h. Further treatment of prepared mesoporous silica was performed using trimethylmethoxysilane (TMMS) to obtain hydrophobic Mesoporous silica. For all synthesized silicas, silica contents were as high as 95 wt %, whereas organic residues were less than 3 wt %. RHA-glycerol showed the highest specific surface area with smallest pore diameter (205.70 m(2)/g, 7.46 nm) when aged for 48 h. The optimal hydrolysis-ageing period of 120 h resulted in 500.7 m(2)/g specific surface area, 0.655 cm(3)/g pore volume and 5.23 nm pore diameter. The surface modification of RHA-glycerol occurred through the reaction with TMMS as confirmed by FTIR (Fourier-transform infrared spectroscopy). Ibuprofen was selected as a model drug for the adsorption experiments. The adsorption under supercritical CO(2) was carried out at isothermal temperature of 40 °C and 100 bar; % ibuprofen loading of TMMS modified mesoporous silica (TMMS-g-MS) was 6 times less than that of mesoporous silica aged for 24 h (MS-24h) due to the hydrophobic nature of modified mesoporous silica, not surface and pore characteristics. The release kinetics of ibuprofen-loaded mesoporous silicas were also investigated in vitro. The release rate of ibuprofen-loaded MS-24h was much faster than that of ibuprofen-loaded TMMS-g-MS, but comparable to the crystalline ibuprofen. The slower release rate was attributed to the diffusion control and the stability of hydrophobic nature of modified silica. This would allow the design of a controlled release drug delivery system.
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spelling pubmed-60732552018-08-13 Hydrophilic and Hydrophobic Mesoporous Silica Derived from Rice Husk Ash as a Potential Drug Carrier Suttiruengwong, Supakij Pivsa-Art, Sommai Chareonpanich, Metta Materials (Basel) Article This work describes the preparation of mesoporous silica by the green reaction of rice husk ash (RHA) with glycerol, followed by the modification and the potential use as a drug carrier. The reaction was carried out at 215 °C for 2 h. The solution was further hydrolyzed with deionized water and aged for various times (24, 48, 120, 360, 528 and 672 h) before calcinations at 500 °C for 24 h. Further treatment of prepared mesoporous silica was performed using trimethylmethoxysilane (TMMS) to obtain hydrophobic Mesoporous silica. For all synthesized silicas, silica contents were as high as 95 wt %, whereas organic residues were less than 3 wt %. RHA-glycerol showed the highest specific surface area with smallest pore diameter (205.70 m(2)/g, 7.46 nm) when aged for 48 h. The optimal hydrolysis-ageing period of 120 h resulted in 500.7 m(2)/g specific surface area, 0.655 cm(3)/g pore volume and 5.23 nm pore diameter. The surface modification of RHA-glycerol occurred through the reaction with TMMS as confirmed by FTIR (Fourier-transform infrared spectroscopy). Ibuprofen was selected as a model drug for the adsorption experiments. The adsorption under supercritical CO(2) was carried out at isothermal temperature of 40 °C and 100 bar; % ibuprofen loading of TMMS modified mesoporous silica (TMMS-g-MS) was 6 times less than that of mesoporous silica aged for 24 h (MS-24h) due to the hydrophobic nature of modified mesoporous silica, not surface and pore characteristics. The release kinetics of ibuprofen-loaded mesoporous silicas were also investigated in vitro. The release rate of ibuprofen-loaded MS-24h was much faster than that of ibuprofen-loaded TMMS-g-MS, but comparable to the crystalline ibuprofen. The slower release rate was attributed to the diffusion control and the stability of hydrophobic nature of modified silica. This would allow the design of a controlled release drug delivery system. MDPI 2018-07-05 /pmc/articles/PMC6073255/ /pubmed/29976886 http://dx.doi.org/10.3390/ma11071142 Text en © 2018 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
Suttiruengwong, Supakij
Pivsa-Art, Sommai
Chareonpanich, Metta
Hydrophilic and Hydrophobic Mesoporous Silica Derived from Rice Husk Ash as a Potential Drug Carrier
title Hydrophilic and Hydrophobic Mesoporous Silica Derived from Rice Husk Ash as a Potential Drug Carrier
title_full Hydrophilic and Hydrophobic Mesoporous Silica Derived from Rice Husk Ash as a Potential Drug Carrier
title_fullStr Hydrophilic and Hydrophobic Mesoporous Silica Derived from Rice Husk Ash as a Potential Drug Carrier
title_full_unstemmed Hydrophilic and Hydrophobic Mesoporous Silica Derived from Rice Husk Ash as a Potential Drug Carrier
title_short Hydrophilic and Hydrophobic Mesoporous Silica Derived from Rice Husk Ash as a Potential Drug Carrier
title_sort hydrophilic and hydrophobic mesoporous silica derived from rice husk ash as a potential drug carrier
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6073255/
https://www.ncbi.nlm.nih.gov/pubmed/29976886
http://dx.doi.org/10.3390/ma11071142
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