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Supramolecular assembly affording a ratiometric two-photon fluorescent nanoprobe for quantitative detection and bioimaging

Fluorescence quantitative analyses for vital biomolecules are in great demand in biomedical science owing to their unique detection advantages with rapid, sensitive, non-damaging and specific identification. However, available fluorescence strategies for quantitative detection are usually hard to de...

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Autores principales: Wang, Peng, Zhang, Cheng, Liu, Hong-Wen, Xiong, Mengyi, Yin, Sheng-Yan, Yang, Yue, Hu, Xiao-Xiao, Yin, Xia, Zhang, Xiao-Bing, Tan, Weihong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5855966/
https://www.ncbi.nlm.nih.gov/pubmed/29568469
http://dx.doi.org/10.1039/c7sc03977h
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author Wang, Peng
Zhang, Cheng
Liu, Hong-Wen
Xiong, Mengyi
Yin, Sheng-Yan
Yang, Yue
Hu, Xiao-Xiao
Yin, Xia
Zhang, Xiao-Bing
Tan, Weihong
author_facet Wang, Peng
Zhang, Cheng
Liu, Hong-Wen
Xiong, Mengyi
Yin, Sheng-Yan
Yang, Yue
Hu, Xiao-Xiao
Yin, Xia
Zhang, Xiao-Bing
Tan, Weihong
author_sort Wang, Peng
collection PubMed
description Fluorescence quantitative analyses for vital biomolecules are in great demand in biomedical science owing to their unique detection advantages with rapid, sensitive, non-damaging and specific identification. However, available fluorescence strategies for quantitative detection are usually hard to design and achieve. Inspired by supramolecular chemistry, a two-photon-excited fluorescent supramolecular nanoplatform (TPSNP) was designed for quantitative analysis with three parts: host molecules (β-CD polymers), a guest fluorophore of sensing probes (Np–Ad) and a guest internal reference (NpRh–Ad). In this strategy, the TPSNP possesses the merits of (i) improved water-solubility and biocompatibility; (ii) increased tissue penetration depth for bioimaging by two-photon excitation; (iii) quantitative and tunable assembly of functional guest molecules to obtain optimized detection conditions; (iv) a common approach to avoid the limitation of complicated design by adjustment of sensing probes; and (v) accurate quantitative analysis by virtue of reference molecules. As a proof-of-concept, we utilized the two-photon fluorescent probe NHS–Ad-based TPSNP-1 to realize accurate quantitative analysis of hydrogen sulfide (H(2)S), with high sensitivity and good selectivity in live cells, deep tissues and ex vivo-dissected organs, suggesting that the TPSNP is an ideal quantitative indicator for clinical samples. What’s more, TPSNP will pave the way for designing and preparing advanced supramolecular sensors for biosensing and biomedicine.
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spelling pubmed-58559662018-03-22 Supramolecular assembly affording a ratiometric two-photon fluorescent nanoprobe for quantitative detection and bioimaging Wang, Peng Zhang, Cheng Liu, Hong-Wen Xiong, Mengyi Yin, Sheng-Yan Yang, Yue Hu, Xiao-Xiao Yin, Xia Zhang, Xiao-Bing Tan, Weihong Chem Sci Chemistry Fluorescence quantitative analyses for vital biomolecules are in great demand in biomedical science owing to their unique detection advantages with rapid, sensitive, non-damaging and specific identification. However, available fluorescence strategies for quantitative detection are usually hard to design and achieve. Inspired by supramolecular chemistry, a two-photon-excited fluorescent supramolecular nanoplatform (TPSNP) was designed for quantitative analysis with three parts: host molecules (β-CD polymers), a guest fluorophore of sensing probes (Np–Ad) and a guest internal reference (NpRh–Ad). In this strategy, the TPSNP possesses the merits of (i) improved water-solubility and biocompatibility; (ii) increased tissue penetration depth for bioimaging by two-photon excitation; (iii) quantitative and tunable assembly of functional guest molecules to obtain optimized detection conditions; (iv) a common approach to avoid the limitation of complicated design by adjustment of sensing probes; and (v) accurate quantitative analysis by virtue of reference molecules. As a proof-of-concept, we utilized the two-photon fluorescent probe NHS–Ad-based TPSNP-1 to realize accurate quantitative analysis of hydrogen sulfide (H(2)S), with high sensitivity and good selectivity in live cells, deep tissues and ex vivo-dissected organs, suggesting that the TPSNP is an ideal quantitative indicator for clinical samples. What’s more, TPSNP will pave the way for designing and preparing advanced supramolecular sensors for biosensing and biomedicine. Royal Society of Chemistry 2017-12-01 2017-10-09 /pmc/articles/PMC5855966/ /pubmed/29568469 http://dx.doi.org/10.1039/c7sc03977h Text en This journal is © The Royal Society of Chemistry 2017 http://creativecommons.org/licenses/by-nc/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution Non Commercial 3.0 Unported Licence (CC BY-NC 3.0)
spellingShingle Chemistry
Wang, Peng
Zhang, Cheng
Liu, Hong-Wen
Xiong, Mengyi
Yin, Sheng-Yan
Yang, Yue
Hu, Xiao-Xiao
Yin, Xia
Zhang, Xiao-Bing
Tan, Weihong
Supramolecular assembly affording a ratiometric two-photon fluorescent nanoprobe for quantitative detection and bioimaging
title Supramolecular assembly affording a ratiometric two-photon fluorescent nanoprobe for quantitative detection and bioimaging
title_full Supramolecular assembly affording a ratiometric two-photon fluorescent nanoprobe for quantitative detection and bioimaging
title_fullStr Supramolecular assembly affording a ratiometric two-photon fluorescent nanoprobe for quantitative detection and bioimaging
title_full_unstemmed Supramolecular assembly affording a ratiometric two-photon fluorescent nanoprobe for quantitative detection and bioimaging
title_short Supramolecular assembly affording a ratiometric two-photon fluorescent nanoprobe for quantitative detection and bioimaging
title_sort supramolecular assembly affording a ratiometric two-photon fluorescent nanoprobe for quantitative detection and bioimaging
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5855966/
https://www.ncbi.nlm.nih.gov/pubmed/29568469
http://dx.doi.org/10.1039/c7sc03977h
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