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Biomimetic Theranostic Agents with Superior NIR-II Photoacoustic and Magnetic Resonance Imaging Performance for Targeted Photothermal Therapy of Prostate Cancer

The accurate diagnosis and treatment of prostate cancer at an early stage is crucial to reduce mortality rates. However, the limited availability of theranostic agents with active tumor-targeting abilities hinders imaging sensitivity and therapeutic efficiency. To address this challenge, we have dev...

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Autores principales: Liu, Ling, Yang, Shangpo, Zheng, Ziliang, Li, Qingshuang, Liu, Chenchen, Hu, Dehong, Liu, Zhou, Zhang, Xiaoping, Zhang, Ruiping, Gao, Duyang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10305050/
https://www.ncbi.nlm.nih.gov/pubmed/37376066
http://dx.doi.org/10.3390/pharmaceutics15061617
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author Liu, Ling
Yang, Shangpo
Zheng, Ziliang
Li, Qingshuang
Liu, Chenchen
Hu, Dehong
Liu, Zhou
Zhang, Xiaoping
Zhang, Ruiping
Gao, Duyang
author_facet Liu, Ling
Yang, Shangpo
Zheng, Ziliang
Li, Qingshuang
Liu, Chenchen
Hu, Dehong
Liu, Zhou
Zhang, Xiaoping
Zhang, Ruiping
Gao, Duyang
author_sort Liu, Ling
collection PubMed
description The accurate diagnosis and treatment of prostate cancer at an early stage is crucial to reduce mortality rates. However, the limited availability of theranostic agents with active tumor-targeting abilities hinders imaging sensitivity and therapeutic efficiency. To address this challenge, we have developed biomimetic cell membrane-modified Fe(2)O(3) nanoclusters implanted in polypyrrole (CM-LFPP), achieving photoacoustic/magnetic resonance dual-modal imaging-guided photothermal therapy of prostate cancer. The CM-LFPP exhibits strong absorption in the second near-infrared window (NIR-II, 1000–1700 nm), showing high photothermal conversion efficiency of up to 78.7% under 1064 nm laser irradiation, excellent photoacoustic imaging capabilities, and good magnetic resonance imaging ability with a T2 relaxivity of up to 48.7 s(−1) mM(−1). Furthermore, the lipid encapsulation and biomimetic cell membrane modification enable CM-LFPP to actively target tumors, leading to a high signal-to-background ratio of ~30.2 for NIR-II photoacoustic imaging. Moreover, the biocompatible CM-LFPP enables low-dose (0.6 W cm(−2)) photothermal therapy of tumors under 1064 nm laser irradiation. This technology offers a promising theranostic agent with remarkable photothermal conversion efficiency in the NIR-II window, providing highly sensitive photoacoustic/magnetic resonance imaging-guided prostate cancer therapy.
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spelling pubmed-103050502023-06-29 Biomimetic Theranostic Agents with Superior NIR-II Photoacoustic and Magnetic Resonance Imaging Performance for Targeted Photothermal Therapy of Prostate Cancer Liu, Ling Yang, Shangpo Zheng, Ziliang Li, Qingshuang Liu, Chenchen Hu, Dehong Liu, Zhou Zhang, Xiaoping Zhang, Ruiping Gao, Duyang Pharmaceutics Article The accurate diagnosis and treatment of prostate cancer at an early stage is crucial to reduce mortality rates. However, the limited availability of theranostic agents with active tumor-targeting abilities hinders imaging sensitivity and therapeutic efficiency. To address this challenge, we have developed biomimetic cell membrane-modified Fe(2)O(3) nanoclusters implanted in polypyrrole (CM-LFPP), achieving photoacoustic/magnetic resonance dual-modal imaging-guided photothermal therapy of prostate cancer. The CM-LFPP exhibits strong absorption in the second near-infrared window (NIR-II, 1000–1700 nm), showing high photothermal conversion efficiency of up to 78.7% under 1064 nm laser irradiation, excellent photoacoustic imaging capabilities, and good magnetic resonance imaging ability with a T2 relaxivity of up to 48.7 s(−1) mM(−1). Furthermore, the lipid encapsulation and biomimetic cell membrane modification enable CM-LFPP to actively target tumors, leading to a high signal-to-background ratio of ~30.2 for NIR-II photoacoustic imaging. Moreover, the biocompatible CM-LFPP enables low-dose (0.6 W cm(−2)) photothermal therapy of tumors under 1064 nm laser irradiation. This technology offers a promising theranostic agent with remarkable photothermal conversion efficiency in the NIR-II window, providing highly sensitive photoacoustic/magnetic resonance imaging-guided prostate cancer therapy. MDPI 2023-05-30 /pmc/articles/PMC10305050/ /pubmed/37376066 http://dx.doi.org/10.3390/pharmaceutics15061617 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Liu, Ling
Yang, Shangpo
Zheng, Ziliang
Li, Qingshuang
Liu, Chenchen
Hu, Dehong
Liu, Zhou
Zhang, Xiaoping
Zhang, Ruiping
Gao, Duyang
Biomimetic Theranostic Agents with Superior NIR-II Photoacoustic and Magnetic Resonance Imaging Performance for Targeted Photothermal Therapy of Prostate Cancer
title Biomimetic Theranostic Agents with Superior NIR-II Photoacoustic and Magnetic Resonance Imaging Performance for Targeted Photothermal Therapy of Prostate Cancer
title_full Biomimetic Theranostic Agents with Superior NIR-II Photoacoustic and Magnetic Resonance Imaging Performance for Targeted Photothermal Therapy of Prostate Cancer
title_fullStr Biomimetic Theranostic Agents with Superior NIR-II Photoacoustic and Magnetic Resonance Imaging Performance for Targeted Photothermal Therapy of Prostate Cancer
title_full_unstemmed Biomimetic Theranostic Agents with Superior NIR-II Photoacoustic and Magnetic Resonance Imaging Performance for Targeted Photothermal Therapy of Prostate Cancer
title_short Biomimetic Theranostic Agents with Superior NIR-II Photoacoustic and Magnetic Resonance Imaging Performance for Targeted Photothermal Therapy of Prostate Cancer
title_sort biomimetic theranostic agents with superior nir-ii photoacoustic and magnetic resonance imaging performance for targeted photothermal therapy of prostate cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10305050/
https://www.ncbi.nlm.nih.gov/pubmed/37376066
http://dx.doi.org/10.3390/pharmaceutics15061617
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