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Dual‐Triggered Near‐Infrared Persistent Luminescence Nanoprobe for Autofluorescence‐Free Imaging‐Guided Precise Therapy of Rheumatoid Arthritis
Rheumatoid arthritis (RA) is a common, chronic, and highly disabling autoimmune disease characterized by difficult treatment, long disease duration, and easy recurrence. The development and application of high‐sensitivity theranostic probes for RA that will facilitate precise monitoring of disease p...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9896051/ https://www.ncbi.nlm.nih.gov/pubmed/36461720 http://dx.doi.org/10.1002/advs.202205320 |
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author | Wang, Ruoping Shi, Junpeng Zhang, Qian Peng, Qiang Sun, Xia Song, Liang Zhang, Yun |
author_facet | Wang, Ruoping Shi, Junpeng Zhang, Qian Peng, Qiang Sun, Xia Song, Liang Zhang, Yun |
author_sort | Wang, Ruoping |
collection | PubMed |
description | Rheumatoid arthritis (RA) is a common, chronic, and highly disabling autoimmune disease characterized by difficult treatment, long disease duration, and easy recurrence. The development and application of high‐sensitivity theranostic probes for RA that will facilitate precise monitoring of disease progression and enable effective treatment are currently hotspots in the field of RA theranostics. In this study, mZMI@HA, a dual‐triggered theranostics nanoprobe, is constructed based on near‐infrared persistent luminescence nanoparticles (NIR‐PLNPs) for precise RA treatment and therapeutic evaluation. This is the first reported use of high‐sensitivity autofluorescence‐free imaging based on NIR‐PLNPs for precise RA treatment and therapeutic evaluation. Compared with the NIR fluorescence imaging probe‐indocyanine green, the signal‐to‐background ratio of persistent luminescence (PersL) imaging is improved nearly 14‐fold. Using PersL imaging to guide photothermal therapy and controllable drug release through NIR/pH‐responsiveness, the progress of collagen‐induced RA is relieved. Additionally, the therapeutic evaluation of RA by PersL imaging is consistent with clinical micro‐computed tomography and histological analyses. This study demonstrates the potential of NIR‐PLNPs for high‐sensitivity imaging‐guided RA treatment, providing a new strategy for RA precise theranostics. |
format | Online Article Text |
id | pubmed-9896051 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98960512023-02-08 Dual‐Triggered Near‐Infrared Persistent Luminescence Nanoprobe for Autofluorescence‐Free Imaging‐Guided Precise Therapy of Rheumatoid Arthritis Wang, Ruoping Shi, Junpeng Zhang, Qian Peng, Qiang Sun, Xia Song, Liang Zhang, Yun Adv Sci (Weinh) Research Articles Rheumatoid arthritis (RA) is a common, chronic, and highly disabling autoimmune disease characterized by difficult treatment, long disease duration, and easy recurrence. The development and application of high‐sensitivity theranostic probes for RA that will facilitate precise monitoring of disease progression and enable effective treatment are currently hotspots in the field of RA theranostics. In this study, mZMI@HA, a dual‐triggered theranostics nanoprobe, is constructed based on near‐infrared persistent luminescence nanoparticles (NIR‐PLNPs) for precise RA treatment and therapeutic evaluation. This is the first reported use of high‐sensitivity autofluorescence‐free imaging based on NIR‐PLNPs for precise RA treatment and therapeutic evaluation. Compared with the NIR fluorescence imaging probe‐indocyanine green, the signal‐to‐background ratio of persistent luminescence (PersL) imaging is improved nearly 14‐fold. Using PersL imaging to guide photothermal therapy and controllable drug release through NIR/pH‐responsiveness, the progress of collagen‐induced RA is relieved. Additionally, the therapeutic evaluation of RA by PersL imaging is consistent with clinical micro‐computed tomography and histological analyses. This study demonstrates the potential of NIR‐PLNPs for high‐sensitivity imaging‐guided RA treatment, providing a new strategy for RA precise theranostics. John Wiley and Sons Inc. 2022-12-03 /pmc/articles/PMC9896051/ /pubmed/36461720 http://dx.doi.org/10.1002/advs.202205320 Text en © 2022 The Authors. Advanced Science published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Wang, Ruoping Shi, Junpeng Zhang, Qian Peng, Qiang Sun, Xia Song, Liang Zhang, Yun Dual‐Triggered Near‐Infrared Persistent Luminescence Nanoprobe for Autofluorescence‐Free Imaging‐Guided Precise Therapy of Rheumatoid Arthritis |
title | Dual‐Triggered Near‐Infrared Persistent Luminescence Nanoprobe for Autofluorescence‐Free Imaging‐Guided Precise Therapy of Rheumatoid Arthritis |
title_full | Dual‐Triggered Near‐Infrared Persistent Luminescence Nanoprobe for Autofluorescence‐Free Imaging‐Guided Precise Therapy of Rheumatoid Arthritis |
title_fullStr | Dual‐Triggered Near‐Infrared Persistent Luminescence Nanoprobe for Autofluorescence‐Free Imaging‐Guided Precise Therapy of Rheumatoid Arthritis |
title_full_unstemmed | Dual‐Triggered Near‐Infrared Persistent Luminescence Nanoprobe for Autofluorescence‐Free Imaging‐Guided Precise Therapy of Rheumatoid Arthritis |
title_short | Dual‐Triggered Near‐Infrared Persistent Luminescence Nanoprobe for Autofluorescence‐Free Imaging‐Guided Precise Therapy of Rheumatoid Arthritis |
title_sort | dual‐triggered near‐infrared persistent luminescence nanoprobe for autofluorescence‐free imaging‐guided precise therapy of rheumatoid arthritis |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9896051/ https://www.ncbi.nlm.nih.gov/pubmed/36461720 http://dx.doi.org/10.1002/advs.202205320 |
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