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Molecular Design of Conjugated Small Molecule Nanoparticles for Synergistically Enhanced PTT/PDT

Simultaneous photothermal therapy (PTT) and photodynamic therapy (PDT) is beneficial for enhanced cancer therapy due to the synergistic effect. Conventional materials developed for synergistic PTT/PDT are generally multicomponent agents that need complicated preparation procedures and be activated b...

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Autores principales: Shao, Wei, Yang, Chuang, Li, Fangyuan, Wu, Jiahe, Wang, Nan, Ding, Qiang, Gao, Jianqing, Ling, Daishun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Singapore 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7770699/
https://www.ncbi.nlm.nih.gov/pubmed/34138129
http://dx.doi.org/10.1007/s40820-020-00474-6
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author Shao, Wei
Yang, Chuang
Li, Fangyuan
Wu, Jiahe
Wang, Nan
Ding, Qiang
Gao, Jianqing
Ling, Daishun
author_facet Shao, Wei
Yang, Chuang
Li, Fangyuan
Wu, Jiahe
Wang, Nan
Ding, Qiang
Gao, Jianqing
Ling, Daishun
author_sort Shao, Wei
collection PubMed
description Simultaneous photothermal therapy (PTT) and photodynamic therapy (PDT) is beneficial for enhanced cancer therapy due to the synergistic effect. Conventional materials developed for synergistic PTT/PDT are generally multicomponent agents that need complicated preparation procedures and be activated by multiple laser sources. The emerging monocomponent diketopyrrolopyrrole (DPP)-based conjugated small molecular agents enable dual PTT/PDT under a single laser irradiation, but suffer from low singlet oxygen quantum yield, which severely restricts the therapeutic efficacy. Herein, we report acceptor-oriented molecular design of a donor–acceptor–donor (D–A–D) conjugated small molecule (IID-ThTPA)-based phototheranostic agent, with isoindigo (IID) as selective acceptor and triphenylamine (TPA) as donor. The strong D–A strength and narrow singlet–triplet energy gap endow IID-ThTPA nanoparticles (IID-ThTPA NPs) high mass extinction coefficient (18.2 L g(−1) cm(−1)), competitive photothermal conversion efficiency (35.4%), and a dramatically enhanced singlet oxygen quantum yield (84.0%) comparing with previously reported monocomponent PTT/PDT agents. Such a high PTT/PDT performance of IID-ThTPA NPs achieved superior tumor cooperative eradicating capability in vitro and in vivo. [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s40820-020-00474-6) contains supplementary material, which is available to authorized users.
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spelling pubmed-77706992021-06-14 Molecular Design of Conjugated Small Molecule Nanoparticles for Synergistically Enhanced PTT/PDT Shao, Wei Yang, Chuang Li, Fangyuan Wu, Jiahe Wang, Nan Ding, Qiang Gao, Jianqing Ling, Daishun Nanomicro Lett Article Simultaneous photothermal therapy (PTT) and photodynamic therapy (PDT) is beneficial for enhanced cancer therapy due to the synergistic effect. Conventional materials developed for synergistic PTT/PDT are generally multicomponent agents that need complicated preparation procedures and be activated by multiple laser sources. The emerging monocomponent diketopyrrolopyrrole (DPP)-based conjugated small molecular agents enable dual PTT/PDT under a single laser irradiation, but suffer from low singlet oxygen quantum yield, which severely restricts the therapeutic efficacy. Herein, we report acceptor-oriented molecular design of a donor–acceptor–donor (D–A–D) conjugated small molecule (IID-ThTPA)-based phototheranostic agent, with isoindigo (IID) as selective acceptor and triphenylamine (TPA) as donor. The strong D–A strength and narrow singlet–triplet energy gap endow IID-ThTPA nanoparticles (IID-ThTPA NPs) high mass extinction coefficient (18.2 L g(−1) cm(−1)), competitive photothermal conversion efficiency (35.4%), and a dramatically enhanced singlet oxygen quantum yield (84.0%) comparing with previously reported monocomponent PTT/PDT agents. Such a high PTT/PDT performance of IID-ThTPA NPs achieved superior tumor cooperative eradicating capability in vitro and in vivo. [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s40820-020-00474-6) contains supplementary material, which is available to authorized users. Springer Singapore 2020-07-13 /pmc/articles/PMC7770699/ /pubmed/34138129 http://dx.doi.org/10.1007/s40820-020-00474-6 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Shao, Wei
Yang, Chuang
Li, Fangyuan
Wu, Jiahe
Wang, Nan
Ding, Qiang
Gao, Jianqing
Ling, Daishun
Molecular Design of Conjugated Small Molecule Nanoparticles for Synergistically Enhanced PTT/PDT
title Molecular Design of Conjugated Small Molecule Nanoparticles for Synergistically Enhanced PTT/PDT
title_full Molecular Design of Conjugated Small Molecule Nanoparticles for Synergistically Enhanced PTT/PDT
title_fullStr Molecular Design of Conjugated Small Molecule Nanoparticles for Synergistically Enhanced PTT/PDT
title_full_unstemmed Molecular Design of Conjugated Small Molecule Nanoparticles for Synergistically Enhanced PTT/PDT
title_short Molecular Design of Conjugated Small Molecule Nanoparticles for Synergistically Enhanced PTT/PDT
title_sort molecular design of conjugated small molecule nanoparticles for synergistically enhanced ptt/pdt
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7770699/
https://www.ncbi.nlm.nih.gov/pubmed/34138129
http://dx.doi.org/10.1007/s40820-020-00474-6
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