Light-Regulated Release of Entrapped Drugs from Photoresponsive Gold Nanoparticles
Release of a payload in a spatiotemporal fashion has a substantial impact on increasing therapeutic efficacy. In this work, a novel monolayer of gold nanoparticles (AuNPs) featuring light-responsive ligands was investigated as a potential drug carrier whose drug release can be triggered by UV light....
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Veröffentlicht in: | Journal of nanomaterials 2016-01, Vol.2016 (2016), p.1-7 |
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creator | Chompoosor, Apiwat Moosophon, Panawan Suchaichit, Nattawut Sreejivungsa, Kaniknun |
description | Release of a payload in a spatiotemporal fashion has a substantial impact on increasing therapeutic efficacy. In this work, a novel monolayer of gold nanoparticles (AuNPs) featuring light-responsive ligands was investigated as a potential drug carrier whose drug release can be triggered by UV light. Hydrophobic molecules were noncovalently entrapped in the compartments of its monolayers. Once irradiated with UV light, the dinitrobenzyl linker was cleaved, leading to release of the entrapped agent. AuNPs were characterized using UV spectrophotometry, TEM, and a zetasizer. A naturally occurring compound extracted from Goniothalamus elegans Ast was chosen as a hydrophobic model drug. Entrapment and release of dye were monitored using fluorimetry. The percent encapsulation of dye was of 13.53%. Entrapped dye can be released upon UV irradiation and can be regulated by changing irradiation time. Up to 83.95±2.2% entrapped dye can be released after irradiation for 20 minutes. In the absence of UV light, dye release was only 19.75%. For comparison purposes, AuNPs having no dinitrobenzyl groups showed a minimal release of 12.23% and 11.69% with and without UV light, respectively. This demonstrated an alternative strategy to encapsulate drugs using a noncovalent approach followed by their controlled release upon UV irradiation. |
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In this work, a novel monolayer of gold nanoparticles (AuNPs) featuring light-responsive ligands was investigated as a potential drug carrier whose drug release can be triggered by UV light. Hydrophobic molecules were noncovalently entrapped in the compartments of its monolayers. Once irradiated with UV light, the dinitrobenzyl linker was cleaved, leading to release of the entrapped agent. AuNPs were characterized using UV spectrophotometry, TEM, and a zetasizer. A naturally occurring compound extracted from Goniothalamus elegans Ast was chosen as a hydrophobic model drug. Entrapment and release of dye were monitored using fluorimetry. The percent encapsulation of dye was of 13.53%. Entrapped dye can be released upon UV irradiation and can be regulated by changing irradiation time. Up to 83.95±2.2% entrapped dye can be released after irradiation for 20 minutes. In the absence of UV light, dye release was only 19.75%. For comparison purposes, AuNPs having no dinitrobenzyl groups showed a minimal release of 12.23% and 11.69% with and without UV light, respectively. This demonstrated an alternative strategy to encapsulate drugs using a noncovalent approach followed by their controlled release upon UV irradiation.</description><identifier>ISSN: 1687-4110</identifier><identifier>EISSN: 1687-4129</identifier><identifier>DOI: 10.1155/2016/4964693</identifier><language>eng</language><publisher>Cairo, Egypt: Hindawi Publishing Corporation</publisher><subject>Drug delivery systems ; Drugs ; Dyes ; Encapsulation ; Gold ; Irradiation ; Monolayers ; Nanomaterials ; Nanoparticles ; Nanotechnology</subject><ispartof>Journal of nanomaterials, 2016-01, Vol.2016 (2016), p.1-7</ispartof><rights>Copyright © 2016 Kaniknun Sreejivungsa et al.</rights><rights>Copyright © 2016 Kaniknun Sreejivungsa et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a466t-59407ceec6b62279d091be186e215cedb9636f8cd76bdd94e17d43d5ce482bf33</citedby><cites>FETCH-LOGICAL-a466t-59407ceec6b62279d091be186e215cedb9636f8cd76bdd94e17d43d5ce482bf33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,27928,27929</link.rule.ids></links><search><contributor>Naik, Rajesh R.</contributor><creatorcontrib>Chompoosor, Apiwat</creatorcontrib><creatorcontrib>Moosophon, Panawan</creatorcontrib><creatorcontrib>Suchaichit, Nattawut</creatorcontrib><creatorcontrib>Sreejivungsa, Kaniknun</creatorcontrib><title>Light-Regulated Release of Entrapped Drugs from Photoresponsive Gold Nanoparticles</title><title>Journal of nanomaterials</title><description>Release of a payload in a spatiotemporal fashion has a substantial impact on increasing therapeutic efficacy. 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For comparison purposes, AuNPs having no dinitrobenzyl groups showed a minimal release of 12.23% and 11.69% with and without UV light, respectively. 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subjects | Drug delivery systems Drugs Dyes Encapsulation Gold Irradiation Monolayers Nanomaterials Nanoparticles Nanotechnology |
title | Light-Regulated Release of Entrapped Drugs from Photoresponsive Gold Nanoparticles |
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