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Study on combination therapy for lung cancer through pemetrexed‐loaded mesoporous polydopamine nanoparticles
Lung cancer is one of the most commonly diagnosed cancers, and surgical resection is the optimal choice for the primary lung tumor. But for the secondary lung cancer, chemotherapy and combined radiotherapy still are the main strategies. To realize the combined treatment for non‐small cell lung cance...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10087741/ https://www.ncbi.nlm.nih.gov/pubmed/36479812 http://dx.doi.org/10.1002/jbm.a.37436 |
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author | Xu, Jian Xu, Wei Wang, Zhiqiang Jiang, Yuequan |
author_facet | Xu, Jian Xu, Wei Wang, Zhiqiang Jiang, Yuequan |
author_sort | Xu, Jian |
collection | PubMed |
description | Lung cancer is one of the most commonly diagnosed cancers, and surgical resection is the optimal choice for the primary lung tumor. But for the secondary lung cancer, chemotherapy and combined radiotherapy still are the main strategies. To realize the combined treatment for non‐small cell lung cancer (NSCLC), in this work, a nanoplatform based on pemetrexed (PE)‐loaded mesoporous polydopamine (MPDA) nanoparticles were investigated. PE, a special therapeutic drug for NSCLC, was loaded into the MPDA nanoparticles via electrostatic attraction and was encapsulated with polyvinyl pyrrolidone (PVP). The results showed that, when irradiating with 808 nm near‐infrared light, the PE loaded MPDA (MPDA@PE@PVP) nanoparticles have excellent photothermal conversion properties, which would result in increase of ambient temperature and could accelerate the release of PE. In vitro cell experiments proved that MPDA@PE@PVP nanoparticles have excellent killing ability for NSCLC A549 cells by the functions of PE and photothermal ability of MPDA nanoparticles. Meanwhile, the intra‐cellular reactive oxygen species (ROS) levels of A549 cells in the MPDA@PE@PVP nanoparticle‐treated group could be promoted significantly after irradiation, leading to the death of A549 cells. In vivo animal model results showed that MPDA@PE@PVP nanoparticles could gather at the tumor site by enhanced permeability and retention (EPR) effect and have significant inhibition ability for lung tumor by synergistic therapy of chemotherapy, photothermal therapy and photodynamic therapy. |
format | Online Article Text |
id | pubmed-10087741 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-100877412023-04-12 Study on combination therapy for lung cancer through pemetrexed‐loaded mesoporous polydopamine nanoparticles Xu, Jian Xu, Wei Wang, Zhiqiang Jiang, Yuequan J Biomed Mater Res A Research Articles Lung cancer is one of the most commonly diagnosed cancers, and surgical resection is the optimal choice for the primary lung tumor. But for the secondary lung cancer, chemotherapy and combined radiotherapy still are the main strategies. To realize the combined treatment for non‐small cell lung cancer (NSCLC), in this work, a nanoplatform based on pemetrexed (PE)‐loaded mesoporous polydopamine (MPDA) nanoparticles were investigated. PE, a special therapeutic drug for NSCLC, was loaded into the MPDA nanoparticles via electrostatic attraction and was encapsulated with polyvinyl pyrrolidone (PVP). The results showed that, when irradiating with 808 nm near‐infrared light, the PE loaded MPDA (MPDA@PE@PVP) nanoparticles have excellent photothermal conversion properties, which would result in increase of ambient temperature and could accelerate the release of PE. In vitro cell experiments proved that MPDA@PE@PVP nanoparticles have excellent killing ability for NSCLC A549 cells by the functions of PE and photothermal ability of MPDA nanoparticles. Meanwhile, the intra‐cellular reactive oxygen species (ROS) levels of A549 cells in the MPDA@PE@PVP nanoparticle‐treated group could be promoted significantly after irradiation, leading to the death of A549 cells. In vivo animal model results showed that MPDA@PE@PVP nanoparticles could gather at the tumor site by enhanced permeability and retention (EPR) effect and have significant inhibition ability for lung tumor by synergistic therapy of chemotherapy, photothermal therapy and photodynamic therapy. John Wiley & Sons, Inc. 2022-08-10 2023-02 /pmc/articles/PMC10087741/ /pubmed/36479812 http://dx.doi.org/10.1002/jbm.a.37436 Text en © 2022 The Authors. Journal of Biomedical Materials Research Part A published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Research Articles Xu, Jian Xu, Wei Wang, Zhiqiang Jiang, Yuequan Study on combination therapy for lung cancer through pemetrexed‐loaded mesoporous polydopamine nanoparticles |
title | Study on combination therapy for lung cancer through pemetrexed‐loaded mesoporous polydopamine nanoparticles |
title_full | Study on combination therapy for lung cancer through pemetrexed‐loaded mesoporous polydopamine nanoparticles |
title_fullStr | Study on combination therapy for lung cancer through pemetrexed‐loaded mesoporous polydopamine nanoparticles |
title_full_unstemmed | Study on combination therapy for lung cancer through pemetrexed‐loaded mesoporous polydopamine nanoparticles |
title_short | Study on combination therapy for lung cancer through pemetrexed‐loaded mesoporous polydopamine nanoparticles |
title_sort | study on combination therapy for lung cancer through pemetrexed‐loaded mesoporous polydopamine nanoparticles |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10087741/ https://www.ncbi.nlm.nih.gov/pubmed/36479812 http://dx.doi.org/10.1002/jbm.a.37436 |
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