Cargando…

A pH-Responsive System Based on Fluorescence Enhanced Gold Nanoparticles for Renal Targeting Drug Delivery and Fibrosis Therapy

BACKGROUND: Stimuli-responsive gold nano-assemblies have attracted attention as drug delivery systems in the biomedical field. However, there are challenges achieving targeted delivery and controllable drug release for specific diseases. MATERIALS AND METHODS: In this study, a glutathione (GSH)-modi...

Descripción completa

Detalles Bibliográficos
Autores principales: Lai, Xuandi, Geng, Xinran, Tan, Lishan, Hu, Jianqiang, Wang, Shubin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7440925/
https://www.ncbi.nlm.nih.gov/pubmed/32884257
http://dx.doi.org/10.2147/IJN.S260069
_version_ 1783573209245810688
author Lai, Xuandi
Geng, Xinran
Tan, Lishan
Hu, Jianqiang
Wang, Shubin
author_facet Lai, Xuandi
Geng, Xinran
Tan, Lishan
Hu, Jianqiang
Wang, Shubin
author_sort Lai, Xuandi
collection PubMed
description BACKGROUND: Stimuli-responsive gold nano-assemblies have attracted attention as drug delivery systems in the biomedical field. However, there are challenges achieving targeted delivery and controllable drug release for specific diseases. MATERIALS AND METHODS: In this study, a glutathione (GSH)-modified fluorescent gold nanoparticle termed AuLA-GSH was prepared and a Co(2+)-induced self-assembly drug delivery platform termed AuLA-GSH-Co was constructed. Both the pH-responsive character and drug loading behavior of AuLA-GSH-Co were studied in vitro. Kidney-targeting capability was investigated in vitro and in vivo. Finally, the anti-fibrosis efficiency of AuLA-GSH-Co in a mouse model of unilateral ureteral obstruction (UUO) was explored. RESULTS: AuLA-GSH-Co was sensitive to pH changes and released Co(2+) in acidic conditions, allowing it to have controllable drug release abilities. AuLA-GSH-Co was found to improve cellular uptake of Co(2+) ions compared to CoCl(2) in vitro. AuLA-GSH exhibited specific renal targeting and prolonged renal retention time with low non-specific accumulation in vivo. Moreover, the anti-fibrosis efficiency of AuLA-GSH-Co was higher compared to CoCl(2) in a mouse model of unilateral ureteral obstruction (UUO). CONCLUSION: AuLA-GSH-Co could greatly enhance drug delivery efficiency with renal targeting capability and obviously relieve renal fibrosis, providing a promising strategy for renal fibrosis therapy.
format Online
Article
Text
id pubmed-7440925
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Dove
record_format MEDLINE/PubMed
spelling pubmed-74409252020-09-02 A pH-Responsive System Based on Fluorescence Enhanced Gold Nanoparticles for Renal Targeting Drug Delivery and Fibrosis Therapy Lai, Xuandi Geng, Xinran Tan, Lishan Hu, Jianqiang Wang, Shubin Int J Nanomedicine Original Research BACKGROUND: Stimuli-responsive gold nano-assemblies have attracted attention as drug delivery systems in the biomedical field. However, there are challenges achieving targeted delivery and controllable drug release for specific diseases. MATERIALS AND METHODS: In this study, a glutathione (GSH)-modified fluorescent gold nanoparticle termed AuLA-GSH was prepared and a Co(2+)-induced self-assembly drug delivery platform termed AuLA-GSH-Co was constructed. Both the pH-responsive character and drug loading behavior of AuLA-GSH-Co were studied in vitro. Kidney-targeting capability was investigated in vitro and in vivo. Finally, the anti-fibrosis efficiency of AuLA-GSH-Co in a mouse model of unilateral ureteral obstruction (UUO) was explored. RESULTS: AuLA-GSH-Co was sensitive to pH changes and released Co(2+) in acidic conditions, allowing it to have controllable drug release abilities. AuLA-GSH-Co was found to improve cellular uptake of Co(2+) ions compared to CoCl(2) in vitro. AuLA-GSH exhibited specific renal targeting and prolonged renal retention time with low non-specific accumulation in vivo. Moreover, the anti-fibrosis efficiency of AuLA-GSH-Co was higher compared to CoCl(2) in a mouse model of unilateral ureteral obstruction (UUO). CONCLUSION: AuLA-GSH-Co could greatly enhance drug delivery efficiency with renal targeting capability and obviously relieve renal fibrosis, providing a promising strategy for renal fibrosis therapy. Dove 2020-08-06 /pmc/articles/PMC7440925/ /pubmed/32884257 http://dx.doi.org/10.2147/IJN.S260069 Text en © 2020 Lai et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Lai, Xuandi
Geng, Xinran
Tan, Lishan
Hu, Jianqiang
Wang, Shubin
A pH-Responsive System Based on Fluorescence Enhanced Gold Nanoparticles for Renal Targeting Drug Delivery and Fibrosis Therapy
title A pH-Responsive System Based on Fluorescence Enhanced Gold Nanoparticles for Renal Targeting Drug Delivery and Fibrosis Therapy
title_full A pH-Responsive System Based on Fluorescence Enhanced Gold Nanoparticles for Renal Targeting Drug Delivery and Fibrosis Therapy
title_fullStr A pH-Responsive System Based on Fluorescence Enhanced Gold Nanoparticles for Renal Targeting Drug Delivery and Fibrosis Therapy
title_full_unstemmed A pH-Responsive System Based on Fluorescence Enhanced Gold Nanoparticles for Renal Targeting Drug Delivery and Fibrosis Therapy
title_short A pH-Responsive System Based on Fluorescence Enhanced Gold Nanoparticles for Renal Targeting Drug Delivery and Fibrosis Therapy
title_sort ph-responsive system based on fluorescence enhanced gold nanoparticles for renal targeting drug delivery and fibrosis therapy
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7440925/
https://www.ncbi.nlm.nih.gov/pubmed/32884257
http://dx.doi.org/10.2147/IJN.S260069
work_keys_str_mv AT laixuandi aphresponsivesystembasedonfluorescenceenhancedgoldnanoparticlesforrenaltargetingdrugdeliveryandfibrosistherapy
AT gengxinran aphresponsivesystembasedonfluorescenceenhancedgoldnanoparticlesforrenaltargetingdrugdeliveryandfibrosistherapy
AT tanlishan aphresponsivesystembasedonfluorescenceenhancedgoldnanoparticlesforrenaltargetingdrugdeliveryandfibrosistherapy
AT hujianqiang aphresponsivesystembasedonfluorescenceenhancedgoldnanoparticlesforrenaltargetingdrugdeliveryandfibrosistherapy
AT wangshubin aphresponsivesystembasedonfluorescenceenhancedgoldnanoparticlesforrenaltargetingdrugdeliveryandfibrosistherapy
AT laixuandi phresponsivesystembasedonfluorescenceenhancedgoldnanoparticlesforrenaltargetingdrugdeliveryandfibrosistherapy
AT gengxinran phresponsivesystembasedonfluorescenceenhancedgoldnanoparticlesforrenaltargetingdrugdeliveryandfibrosistherapy
AT tanlishan phresponsivesystembasedonfluorescenceenhancedgoldnanoparticlesforrenaltargetingdrugdeliveryandfibrosistherapy
AT hujianqiang phresponsivesystembasedonfluorescenceenhancedgoldnanoparticlesforrenaltargetingdrugdeliveryandfibrosistherapy
AT wangshubin phresponsivesystembasedonfluorescenceenhancedgoldnanoparticlesforrenaltargetingdrugdeliveryandfibrosistherapy