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Folic acid-conjugated gold nanorod@polypyrrole@Fe(3)O(4) nanocomposites for targeted MR/CT/PA multimodal imaging and chemo-photothermal therapy
Integrating multimodal bioimaging and different therapies into one nanoplatform is a promising strategy for biomedical applications, but remains a great challenge. Herein, we have synthesized a biocompatible folic acid (FA) functionalized gold nanorod@polypyrrole@Fe(3)O(4) (GNR@PPy@Fe(3)O(4)-FA) nan...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9065171/ https://www.ncbi.nlm.nih.gov/pubmed/35516886 http://dx.doi.org/10.1039/c9ra00541b |
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author | Cao, Wei Wang, Xuandong Song, Liang Wang, Peiyuan Hou, Xuemei Zhang, Huicong Tian, Xiangdong Liu, Xiaolong Zhang, Yun |
author_facet | Cao, Wei Wang, Xuandong Song, Liang Wang, Peiyuan Hou, Xuemei Zhang, Huicong Tian, Xiangdong Liu, Xiaolong Zhang, Yun |
author_sort | Cao, Wei |
collection | PubMed |
description | Integrating multimodal bioimaging and different therapies into one nanoplatform is a promising strategy for biomedical applications, but remains a great challenge. Herein, we have synthesized a biocompatible folic acid (FA) functionalized gold nanorod@polypyrrole@Fe(3)O(4) (GNR@PPy@Fe(3)O(4)-FA) nanocomposite through a facile method. The conjugated FA has endowed the nanocomposite with the ability to recognize targeted cancer cells. Importantly, the nanocomposite has been successfully utilized for magnetic resonance (MR), computed tomography (CT) and photoacoustic (PA) multimodal imaging. Moreover, the GNR@PPy@Fe(3)O(4)-DOX nanocomposite shows pH-responsive chemotherapy and enables the integration of photothermal therapy and chemotherapy to achieve superior antitumor efficacy. The GNR@PPy@Fe(3)O(4)-DOX nanocomposites have a drug release of 23.64%, and the photothermal efficiency of the GNR@PPy@Fe(3)O(4) nanocomposites reaches 51.46%. Cell viability decreases to 15.83% and 16.47% because of the combination of chemo-photothermal therapy effects. Moreover, the GNR@PPy@Fe(3)O(4)-DOX-FA nanocomposite could target cancer cells via folic acid and under a magnetic field. The in vivo multimodal imaging and chemo-photothermal therapy effects showed that the GNR@PPy@Fe(3)O(4)-DOX-FA nanocomposites are a good contrast and theranostic agent. Thus, this multifunctional nanocomposite could be a promising theranostic platform for cancer diagnosis and therapy. |
format | Online Article Text |
id | pubmed-9065171 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90651712022-05-04 Folic acid-conjugated gold nanorod@polypyrrole@Fe(3)O(4) nanocomposites for targeted MR/CT/PA multimodal imaging and chemo-photothermal therapy Cao, Wei Wang, Xuandong Song, Liang Wang, Peiyuan Hou, Xuemei Zhang, Huicong Tian, Xiangdong Liu, Xiaolong Zhang, Yun RSC Adv Chemistry Integrating multimodal bioimaging and different therapies into one nanoplatform is a promising strategy for biomedical applications, but remains a great challenge. Herein, we have synthesized a biocompatible folic acid (FA) functionalized gold nanorod@polypyrrole@Fe(3)O(4) (GNR@PPy@Fe(3)O(4)-FA) nanocomposite through a facile method. The conjugated FA has endowed the nanocomposite with the ability to recognize targeted cancer cells. Importantly, the nanocomposite has been successfully utilized for magnetic resonance (MR), computed tomography (CT) and photoacoustic (PA) multimodal imaging. Moreover, the GNR@PPy@Fe(3)O(4)-DOX nanocomposite shows pH-responsive chemotherapy and enables the integration of photothermal therapy and chemotherapy to achieve superior antitumor efficacy. The GNR@PPy@Fe(3)O(4)-DOX nanocomposites have a drug release of 23.64%, and the photothermal efficiency of the GNR@PPy@Fe(3)O(4) nanocomposites reaches 51.46%. Cell viability decreases to 15.83% and 16.47% because of the combination of chemo-photothermal therapy effects. Moreover, the GNR@PPy@Fe(3)O(4)-DOX-FA nanocomposite could target cancer cells via folic acid and under a magnetic field. The in vivo multimodal imaging and chemo-photothermal therapy effects showed that the GNR@PPy@Fe(3)O(4)-DOX-FA nanocomposites are a good contrast and theranostic agent. Thus, this multifunctional nanocomposite could be a promising theranostic platform for cancer diagnosis and therapy. The Royal Society of Chemistry 2019-06-17 /pmc/articles/PMC9065171/ /pubmed/35516886 http://dx.doi.org/10.1039/c9ra00541b Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Cao, Wei Wang, Xuandong Song, Liang Wang, Peiyuan Hou, Xuemei Zhang, Huicong Tian, Xiangdong Liu, Xiaolong Zhang, Yun Folic acid-conjugated gold nanorod@polypyrrole@Fe(3)O(4) nanocomposites for targeted MR/CT/PA multimodal imaging and chemo-photothermal therapy |
title | Folic acid-conjugated gold nanorod@polypyrrole@Fe(3)O(4) nanocomposites for targeted MR/CT/PA multimodal imaging and chemo-photothermal therapy |
title_full | Folic acid-conjugated gold nanorod@polypyrrole@Fe(3)O(4) nanocomposites for targeted MR/CT/PA multimodal imaging and chemo-photothermal therapy |
title_fullStr | Folic acid-conjugated gold nanorod@polypyrrole@Fe(3)O(4) nanocomposites for targeted MR/CT/PA multimodal imaging and chemo-photothermal therapy |
title_full_unstemmed | Folic acid-conjugated gold nanorod@polypyrrole@Fe(3)O(4) nanocomposites for targeted MR/CT/PA multimodal imaging and chemo-photothermal therapy |
title_short | Folic acid-conjugated gold nanorod@polypyrrole@Fe(3)O(4) nanocomposites for targeted MR/CT/PA multimodal imaging and chemo-photothermal therapy |
title_sort | folic acid-conjugated gold nanorod@polypyrrole@fe(3)o(4) nanocomposites for targeted mr/ct/pa multimodal imaging and chemo-photothermal therapy |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9065171/ https://www.ncbi.nlm.nih.gov/pubmed/35516886 http://dx.doi.org/10.1039/c9ra00541b |
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