Cargando…

Dual Stimuli-Triggered Nanogels in Response to Temperature and pH Changes for Controlled Drug Release

Poly-N-isopropyl acrylamide (PNIPAM) nanogels have been modified with different acrylic acid (AAc) contents for the efficient control of lower critical solution temperature (LCST). In this study, PNIPAM-co-AAc nanogels nanogels showed two volume phase transitions in comparison with PNIPAM. The trans...

Descripción completa

Detalles Bibliográficos
Autores principales: Kim, Yun Kyoung, Kim, Eun-Joong, Lim, Jae Hyun, Cho, Heui Kyoung, Hong, Woo Jin, Jeon, Hyang Hwa, Chung, Bong Geun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6399374/
https://www.ncbi.nlm.nih.gov/pubmed/30830486
http://dx.doi.org/10.1186/s11671-019-2909-y
_version_ 1783399748093345792
author Kim, Yun Kyoung
Kim, Eun-Joong
Lim, Jae Hyun
Cho, Heui Kyoung
Hong, Woo Jin
Jeon, Hyang Hwa
Chung, Bong Geun
author_facet Kim, Yun Kyoung
Kim, Eun-Joong
Lim, Jae Hyun
Cho, Heui Kyoung
Hong, Woo Jin
Jeon, Hyang Hwa
Chung, Bong Geun
author_sort Kim, Yun Kyoung
collection PubMed
description Poly-N-isopropyl acrylamide (PNIPAM) nanogels have been modified with different acrylic acid (AAc) contents for the efficient control of lower critical solution temperature (LCST). In this study, PNIPAM-co-AAc nanogels nanogels showed two volume phase transitions in comparison with PNIPAM. The transition temperature of PNIPAM nanogels was increased with AAc contents. The controlled drug release performance of PNIPAM-co-AAc nanogels loaded with β-lapachone was attributed to the AAc content ratio and was efficiently triggered in response to temperature and pH. Moreover, a colorimetric cell proliferation assay and direct fluorescence-based live/dead staining were used to confirm the concurrence on drug release profiles. Finally, PNIPAM-co-AAc20 showed a relatively low level of drug release in the range of acidic to neutral pH at body temperature, while maximizing drug release at basic pH. Therefore, we demonstrated that the PNIPAM-based nanogel with the temperature- and pH-responsive features could be a promising nanocarrier for potential intestine-specific drug delivery. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s11671-019-2909-y) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-6399374
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Springer US
record_format MEDLINE/PubMed
spelling pubmed-63993742019-03-22 Dual Stimuli-Triggered Nanogels in Response to Temperature and pH Changes for Controlled Drug Release Kim, Yun Kyoung Kim, Eun-Joong Lim, Jae Hyun Cho, Heui Kyoung Hong, Woo Jin Jeon, Hyang Hwa Chung, Bong Geun Nanoscale Res Lett Nano Express Poly-N-isopropyl acrylamide (PNIPAM) nanogels have been modified with different acrylic acid (AAc) contents for the efficient control of lower critical solution temperature (LCST). In this study, PNIPAM-co-AAc nanogels nanogels showed two volume phase transitions in comparison with PNIPAM. The transition temperature of PNIPAM nanogels was increased with AAc contents. The controlled drug release performance of PNIPAM-co-AAc nanogels loaded with β-lapachone was attributed to the AAc content ratio and was efficiently triggered in response to temperature and pH. Moreover, a colorimetric cell proliferation assay and direct fluorescence-based live/dead staining were used to confirm the concurrence on drug release profiles. Finally, PNIPAM-co-AAc20 showed a relatively low level of drug release in the range of acidic to neutral pH at body temperature, while maximizing drug release at basic pH. Therefore, we demonstrated that the PNIPAM-based nanogel with the temperature- and pH-responsive features could be a promising nanocarrier for potential intestine-specific drug delivery. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s11671-019-2909-y) contains supplementary material, which is available to authorized users. Springer US 2019-03-04 /pmc/articles/PMC6399374/ /pubmed/30830486 http://dx.doi.org/10.1186/s11671-019-2909-y Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Nano Express
Kim, Yun Kyoung
Kim, Eun-Joong
Lim, Jae Hyun
Cho, Heui Kyoung
Hong, Woo Jin
Jeon, Hyang Hwa
Chung, Bong Geun
Dual Stimuli-Triggered Nanogels in Response to Temperature and pH Changes for Controlled Drug Release
title Dual Stimuli-Triggered Nanogels in Response to Temperature and pH Changes for Controlled Drug Release
title_full Dual Stimuli-Triggered Nanogels in Response to Temperature and pH Changes for Controlled Drug Release
title_fullStr Dual Stimuli-Triggered Nanogels in Response to Temperature and pH Changes for Controlled Drug Release
title_full_unstemmed Dual Stimuli-Triggered Nanogels in Response to Temperature and pH Changes for Controlled Drug Release
title_short Dual Stimuli-Triggered Nanogels in Response to Temperature and pH Changes for Controlled Drug Release
title_sort dual stimuli-triggered nanogels in response to temperature and ph changes for controlled drug release
topic Nano Express
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6399374/
https://www.ncbi.nlm.nih.gov/pubmed/30830486
http://dx.doi.org/10.1186/s11671-019-2909-y
work_keys_str_mv AT kimyunkyoung dualstimulitriggerednanogelsinresponsetotemperatureandphchangesforcontrolleddrugrelease
AT kimeunjoong dualstimulitriggerednanogelsinresponsetotemperatureandphchangesforcontrolleddrugrelease
AT limjaehyun dualstimulitriggerednanogelsinresponsetotemperatureandphchangesforcontrolleddrugrelease
AT choheuikyoung dualstimulitriggerednanogelsinresponsetotemperatureandphchangesforcontrolleddrugrelease
AT hongwoojin dualstimulitriggerednanogelsinresponsetotemperatureandphchangesforcontrolleddrugrelease
AT jeonhyanghwa dualstimulitriggerednanogelsinresponsetotemperatureandphchangesforcontrolleddrugrelease
AT chungbonggeun dualstimulitriggerednanogelsinresponsetotemperatureandphchangesforcontrolleddrugrelease