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Graphene oxide loaded with tumor-targeted peptide and anti-cancer drugs for cancer target therapy
In the present work, we constructed nanoscale graphene oxide (NGO) as a drug nanocarrier to improve the process of tumor-targeted drug releases, promote cellular uptake and accumulation of chemotherapy drugs in tumor tissues, and reduce the toxic effects of chemotherapy drugs on normal cells. Hence,...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7813822/ https://www.ncbi.nlm.nih.gov/pubmed/33462277 http://dx.doi.org/10.1038/s41598-021-81218-3 |
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author | Li, Ran Wang, Yimei Du, Jie Wang, Xiangyu Duan, Ailin Gao, Ruifang Liu, Junyu Li, Bing |
author_facet | Li, Ran Wang, Yimei Du, Jie Wang, Xiangyu Duan, Ailin Gao, Ruifang Liu, Junyu Li, Bing |
author_sort | Li, Ran |
collection | PubMed |
description | In the present work, we constructed nanoscale graphene oxide (NGO) as a drug nanocarrier to improve the process of tumor-targeted drug releases, promote cellular uptake and accumulation of chemotherapy drugs in tumor tissues, and reduce the toxic effects of chemotherapy drugs on normal cells. Hence, great stability was obtained in the biological solution. Moreover, we designed an effective nanoparticle system for the doxorubicin (DOX) delivery targeting the oral squamous cell carcinoma (OSCC) by mediating the HN-1 (TSPLNIHNGQKL) through hydrogen and π–π bonds. DOX@NGO-PEG-HN-1 showed significantly higher cellular uptakes and cytotoxicity in OSCC cells (CAL-27 and SCC-25), compared to free DOX. Moreover, HN-1 showed considerable tumor-targeting and competition inhibition phenomenon. As we expected, the nanocarrier showed pH-responsive drug release. In total, our study represented a good technique to construct OSCC-targeted delivery of nanoparticles and improve the anticancer medicines’ efficiency. |
format | Online Article Text |
id | pubmed-7813822 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-78138222021-01-21 Graphene oxide loaded with tumor-targeted peptide and anti-cancer drugs for cancer target therapy Li, Ran Wang, Yimei Du, Jie Wang, Xiangyu Duan, Ailin Gao, Ruifang Liu, Junyu Li, Bing Sci Rep Article In the present work, we constructed nanoscale graphene oxide (NGO) as a drug nanocarrier to improve the process of tumor-targeted drug releases, promote cellular uptake and accumulation of chemotherapy drugs in tumor tissues, and reduce the toxic effects of chemotherapy drugs on normal cells. Hence, great stability was obtained in the biological solution. Moreover, we designed an effective nanoparticle system for the doxorubicin (DOX) delivery targeting the oral squamous cell carcinoma (OSCC) by mediating the HN-1 (TSPLNIHNGQKL) through hydrogen and π–π bonds. DOX@NGO-PEG-HN-1 showed significantly higher cellular uptakes and cytotoxicity in OSCC cells (CAL-27 and SCC-25), compared to free DOX. Moreover, HN-1 showed considerable tumor-targeting and competition inhibition phenomenon. As we expected, the nanocarrier showed pH-responsive drug release. In total, our study represented a good technique to construct OSCC-targeted delivery of nanoparticles and improve the anticancer medicines’ efficiency. Nature Publishing Group UK 2021-01-18 /pmc/articles/PMC7813822/ /pubmed/33462277 http://dx.doi.org/10.1038/s41598-021-81218-3 Text en © The Author(s) 2021 Open Access This 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 Li, Ran Wang, Yimei Du, Jie Wang, Xiangyu Duan, Ailin Gao, Ruifang Liu, Junyu Li, Bing Graphene oxide loaded with tumor-targeted peptide and anti-cancer drugs for cancer target therapy |
title | Graphene oxide loaded with tumor-targeted peptide and anti-cancer drugs for cancer target therapy |
title_full | Graphene oxide loaded with tumor-targeted peptide and anti-cancer drugs for cancer target therapy |
title_fullStr | Graphene oxide loaded with tumor-targeted peptide and anti-cancer drugs for cancer target therapy |
title_full_unstemmed | Graphene oxide loaded with tumor-targeted peptide and anti-cancer drugs for cancer target therapy |
title_short | Graphene oxide loaded with tumor-targeted peptide and anti-cancer drugs for cancer target therapy |
title_sort | graphene oxide loaded with tumor-targeted peptide and anti-cancer drugs for cancer target therapy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7813822/ https://www.ncbi.nlm.nih.gov/pubmed/33462277 http://dx.doi.org/10.1038/s41598-021-81218-3 |
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