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Synthesis and Characterization of Water-Soluble Polythiophene Derivatives for Cell Imaging
In this work, four water-soluble polythiophene derivatives (PT, PT-DDA, PT-ADA, and PT-ADA-PPR) with different pendant moieties were synthesized via oxidative copolymerization by FeCl(3). By increasing the hydrophobic ability of side chain moieties, there is a gradually blue shift for the maximum ab...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5154596/ https://www.ncbi.nlm.nih.gov/pubmed/25557020 http://dx.doi.org/10.1038/srep07617 |
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author | Wang, Fengyan Li, Meng Wang, Bing Zhang, Jiangyan Cheng, Yongqiang Liu, Libing Lv, Fengting Wang, Shu |
author_facet | Wang, Fengyan Li, Meng Wang, Bing Zhang, Jiangyan Cheng, Yongqiang Liu, Libing Lv, Fengting Wang, Shu |
author_sort | Wang, Fengyan |
collection | PubMed |
description | In this work, four water-soluble polythiophene derivatives (PT, PT-DDA, PT-ADA, and PT-ADA-PPR) with different pendant moieties were synthesized via oxidative copolymerization by FeCl(3). By increasing the hydrophobic ability of side chain moieties, there is a gradually blue shift for the maximum absorption wavelength and red shift for the maximum emission wavelength, a reducing trend for fluorescence quantum yields, a growing trend for Stokes shift, and an increasing trend for the mean sizes in the order of PT, PT-ADA, and PT-DDA. All the synthesized polymers show low toxicity and good photostability and accumulate in the lysosomes of A549 cells. Furthermore, the introduction of porphyrin group to PT-ADA side chain (PT-ADA-PPR) broadens the absorption and emission ranges of PT-ADA. PT-ADA-PPR could be excited at two different excitation wavelengths (488 nm and 559 nm) and exhibits two emission pathways, and dual-color fluorescence images (orange and red) of PT-ADA-PPR accumulated in A549 cells are observed. Thus, PT-ADA-PPR could be used as an excellent dual-color fluorescent and lysosome-specific imaging material. |
format | Online Article Text |
id | pubmed-5154596 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-51545962016-12-20 Synthesis and Characterization of Water-Soluble Polythiophene Derivatives for Cell Imaging Wang, Fengyan Li, Meng Wang, Bing Zhang, Jiangyan Cheng, Yongqiang Liu, Libing Lv, Fengting Wang, Shu Sci Rep Article In this work, four water-soluble polythiophene derivatives (PT, PT-DDA, PT-ADA, and PT-ADA-PPR) with different pendant moieties were synthesized via oxidative copolymerization by FeCl(3). By increasing the hydrophobic ability of side chain moieties, there is a gradually blue shift for the maximum absorption wavelength and red shift for the maximum emission wavelength, a reducing trend for fluorescence quantum yields, a growing trend for Stokes shift, and an increasing trend for the mean sizes in the order of PT, PT-ADA, and PT-DDA. All the synthesized polymers show low toxicity and good photostability and accumulate in the lysosomes of A549 cells. Furthermore, the introduction of porphyrin group to PT-ADA side chain (PT-ADA-PPR) broadens the absorption and emission ranges of PT-ADA. PT-ADA-PPR could be excited at two different excitation wavelengths (488 nm and 559 nm) and exhibits two emission pathways, and dual-color fluorescence images (orange and red) of PT-ADA-PPR accumulated in A549 cells are observed. Thus, PT-ADA-PPR could be used as an excellent dual-color fluorescent and lysosome-specific imaging material. Nature Publishing Group 2015-01-05 /pmc/articles/PMC5154596/ /pubmed/25557020 http://dx.doi.org/10.1038/srep07617 Text en Copyright © 2014, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-sa/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/ |
spellingShingle | Article Wang, Fengyan Li, Meng Wang, Bing Zhang, Jiangyan Cheng, Yongqiang Liu, Libing Lv, Fengting Wang, Shu Synthesis and Characterization of Water-Soluble Polythiophene Derivatives for Cell Imaging |
title | Synthesis and Characterization of Water-Soluble Polythiophene Derivatives for Cell Imaging |
title_full | Synthesis and Characterization of Water-Soluble Polythiophene Derivatives for Cell Imaging |
title_fullStr | Synthesis and Characterization of Water-Soluble Polythiophene Derivatives for Cell Imaging |
title_full_unstemmed | Synthesis and Characterization of Water-Soluble Polythiophene Derivatives for Cell Imaging |
title_short | Synthesis and Characterization of Water-Soluble Polythiophene Derivatives for Cell Imaging |
title_sort | synthesis and characterization of water-soluble polythiophene derivatives for cell imaging |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5154596/ https://www.ncbi.nlm.nih.gov/pubmed/25557020 http://dx.doi.org/10.1038/srep07617 |
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