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Enhanced cytotoxic effect of doxorubicin conjugated gold nanoparticles on breast cancer model
BACKGROUND: The difficulty of achieving targeted drug delivery following administration of presently marketed anticancer therapeutics is still a concern. Metallic nanoparticles (NPs) appear to be promising in this regard. The present study focused on the use of gold nanoparticles (AuNPs) as a drug c...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9648023/ https://www.ncbi.nlm.nih.gov/pubmed/36352463 http://dx.doi.org/10.1186/s13065-022-00889-9 |
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author | Faid, Amna H. Shouman, Samia A. Badr, Yehia A. Sharaky, Marwa |
author_facet | Faid, Amna H. Shouman, Samia A. Badr, Yehia A. Sharaky, Marwa |
author_sort | Faid, Amna H. |
collection | PubMed |
description | BACKGROUND: The difficulty of achieving targeted drug delivery following administration of presently marketed anticancer therapeutics is still a concern. Metallic nanoparticles (NPs) appear to be promising in this regard. The present study focused on the use of gold nanoparticles (AuNPs) as a drug carrier for anticancer Doxorubicin (DOX) forming DOX–AuNPs nanocomposite. The anticancer effect of the prepared nanocomposite was evaluated using SRP essay on breast cancer cell line (MCF7) for different incubation times (24 h,48, and72hr). The prepared DOX–AuNPs nanocomposite was investigated by UV–visible spectroscopy, TEM, fluorescence spectroscopy, and FTIR spectroscopy. RESULTS: Our results showed that the prepared AuNPs and DOX–AuNPs nanocomposite have spherical and small size10 ± 2 nm and 12 ± 2 nm respectively. The potential cytotoxicity of the DOX-AuNPs nanocomposite on the MCF7 cell line was significantly increased compared to free DOX. The 20 µM DOX- AuNPs nanocomposite produced a similar decrease in cell survival as 80 µM free DOX. CONCLUSION: Future work is in progress to investigate the positive effects of the prepared nanocomposite for chemo-photothermal combination treatment. |
format | Online Article Text |
id | pubmed-9648023 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-96480232022-11-15 Enhanced cytotoxic effect of doxorubicin conjugated gold nanoparticles on breast cancer model Faid, Amna H. Shouman, Samia A. Badr, Yehia A. Sharaky, Marwa BMC Chem Research BACKGROUND: The difficulty of achieving targeted drug delivery following administration of presently marketed anticancer therapeutics is still a concern. Metallic nanoparticles (NPs) appear to be promising in this regard. The present study focused on the use of gold nanoparticles (AuNPs) as a drug carrier for anticancer Doxorubicin (DOX) forming DOX–AuNPs nanocomposite. The anticancer effect of the prepared nanocomposite was evaluated using SRP essay on breast cancer cell line (MCF7) for different incubation times (24 h,48, and72hr). The prepared DOX–AuNPs nanocomposite was investigated by UV–visible spectroscopy, TEM, fluorescence spectroscopy, and FTIR spectroscopy. RESULTS: Our results showed that the prepared AuNPs and DOX–AuNPs nanocomposite have spherical and small size10 ± 2 nm and 12 ± 2 nm respectively. The potential cytotoxicity of the DOX-AuNPs nanocomposite on the MCF7 cell line was significantly increased compared to free DOX. The 20 µM DOX- AuNPs nanocomposite produced a similar decrease in cell survival as 80 µM free DOX. CONCLUSION: Future work is in progress to investigate the positive effects of the prepared nanocomposite for chemo-photothermal combination treatment. Springer International Publishing 2022-11-09 /pmc/articles/PMC9648023/ /pubmed/36352463 http://dx.doi.org/10.1186/s13065-022-00889-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Faid, Amna H. Shouman, Samia A. Badr, Yehia A. Sharaky, Marwa Enhanced cytotoxic effect of doxorubicin conjugated gold nanoparticles on breast cancer model |
title | Enhanced cytotoxic effect of doxorubicin conjugated gold nanoparticles on breast cancer model |
title_full | Enhanced cytotoxic effect of doxorubicin conjugated gold nanoparticles on breast cancer model |
title_fullStr | Enhanced cytotoxic effect of doxorubicin conjugated gold nanoparticles on breast cancer model |
title_full_unstemmed | Enhanced cytotoxic effect of doxorubicin conjugated gold nanoparticles on breast cancer model |
title_short | Enhanced cytotoxic effect of doxorubicin conjugated gold nanoparticles on breast cancer model |
title_sort | enhanced cytotoxic effect of doxorubicin conjugated gold nanoparticles on breast cancer model |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9648023/ https://www.ncbi.nlm.nih.gov/pubmed/36352463 http://dx.doi.org/10.1186/s13065-022-00889-9 |
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