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Tumor Cell Distinguishable Nanomedicine Integrating Chemotherapeutic Sensitization and Protection
Theoretically, with a high enough drug dosage, cancer cells could be eliminated. However, the dosages that can be administered are limited by the therapeutic efficacy and side effects of the given drug. Herein, a nanomedicine integrating chemotherapeutic sensitization and protection was developed to...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8631718/ https://www.ncbi.nlm.nih.gov/pubmed/34858963 http://dx.doi.org/10.3389/fbioe.2021.773021 |
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author | Liu, Sen Shen, Can Qian, Cheng Wang, Jianquan Yang, Zhongmei Wei, Yanchun Quan, Li Pan, Changjiang Hu, Yong Ye, Wei |
author_facet | Liu, Sen Shen, Can Qian, Cheng Wang, Jianquan Yang, Zhongmei Wei, Yanchun Quan, Li Pan, Changjiang Hu, Yong Ye, Wei |
author_sort | Liu, Sen |
collection | PubMed |
description | Theoretically, with a high enough drug dosage, cancer cells could be eliminated. However, the dosages that can be administered are limited by the therapeutic efficacy and side effects of the given drug. Herein, a nanomedicine integrating chemotherapeutic sensitization and protection was developed to relieve the limitation of administration dosage and to improve the efficacy of chemotherapy. The nanomedicine was endowed with the function of synergistically controlled release of CO and drugs under near-infrared (NIR) light irradiation. CO photo-induced release system (COPIRS) was synthesized by constructing an electron excitation–electron transfer group–electron-induced CO release structure and was used as the hydrophobic part, and then hydrophilic polymer (polyethylene glycol; PEG) was introduced by a thermal-responsive groups (DA group), forming a near-infrared-induced burst-release nanocarrier. In vitro and in vivo experiments showed that the nanomedicine can distinguish between tumor and normal cells and regulates the resistance of these different cells through the controlled release of carbonic oxide (CO), simultaneously enhancing the efficacy of chemotherapy drugs on tumor cells and chemotherapeutic protection on normal cells. This strategy could solve the current limitations on dosages due to toxicity and provide a solution for tumor cure by chemotherapy. |
format | Online Article Text |
id | pubmed-8631718 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-86317182021-12-01 Tumor Cell Distinguishable Nanomedicine Integrating Chemotherapeutic Sensitization and Protection Liu, Sen Shen, Can Qian, Cheng Wang, Jianquan Yang, Zhongmei Wei, Yanchun Quan, Li Pan, Changjiang Hu, Yong Ye, Wei Front Bioeng Biotechnol Bioengineering and Biotechnology Theoretically, with a high enough drug dosage, cancer cells could be eliminated. However, the dosages that can be administered are limited by the therapeutic efficacy and side effects of the given drug. Herein, a nanomedicine integrating chemotherapeutic sensitization and protection was developed to relieve the limitation of administration dosage and to improve the efficacy of chemotherapy. The nanomedicine was endowed with the function of synergistically controlled release of CO and drugs under near-infrared (NIR) light irradiation. CO photo-induced release system (COPIRS) was synthesized by constructing an electron excitation–electron transfer group–electron-induced CO release structure and was used as the hydrophobic part, and then hydrophilic polymer (polyethylene glycol; PEG) was introduced by a thermal-responsive groups (DA group), forming a near-infrared-induced burst-release nanocarrier. In vitro and in vivo experiments showed that the nanomedicine can distinguish between tumor and normal cells and regulates the resistance of these different cells through the controlled release of carbonic oxide (CO), simultaneously enhancing the efficacy of chemotherapy drugs on tumor cells and chemotherapeutic protection on normal cells. This strategy could solve the current limitations on dosages due to toxicity and provide a solution for tumor cure by chemotherapy. Frontiers Media S.A. 2021-11-08 /pmc/articles/PMC8631718/ /pubmed/34858963 http://dx.doi.org/10.3389/fbioe.2021.773021 Text en Copyright © 2021 Liu, Shen, Qian, Wang, Yang, Wei, Quan, Pan, Hu and Ye. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Bioengineering and Biotechnology Liu, Sen Shen, Can Qian, Cheng Wang, Jianquan Yang, Zhongmei Wei, Yanchun Quan, Li Pan, Changjiang Hu, Yong Ye, Wei Tumor Cell Distinguishable Nanomedicine Integrating Chemotherapeutic Sensitization and Protection |
title | Tumor Cell Distinguishable Nanomedicine Integrating Chemotherapeutic Sensitization and Protection |
title_full | Tumor Cell Distinguishable Nanomedicine Integrating Chemotherapeutic Sensitization and Protection |
title_fullStr | Tumor Cell Distinguishable Nanomedicine Integrating Chemotherapeutic Sensitization and Protection |
title_full_unstemmed | Tumor Cell Distinguishable Nanomedicine Integrating Chemotherapeutic Sensitization and Protection |
title_short | Tumor Cell Distinguishable Nanomedicine Integrating Chemotherapeutic Sensitization and Protection |
title_sort | tumor cell distinguishable nanomedicine integrating chemotherapeutic sensitization and protection |
topic | Bioengineering and Biotechnology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8631718/ https://www.ncbi.nlm.nih.gov/pubmed/34858963 http://dx.doi.org/10.3389/fbioe.2021.773021 |
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