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Doxorubicin-loaded gold nanorods: a multifunctional chemo-photothermal nanoplatform for cancer management
Two of the limitations associated with cancer treatment are the low efficacy and the high dose-related side effects of anticancer drugs. The purpose of the current study was to fabricate biocompatible multifunctional drug-loaded nanoscale moieties for co-therapy (chemo-photothermal therapy) with max...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Beilstein-Institut
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8022204/ https://www.ncbi.nlm.nih.gov/pubmed/34012759 http://dx.doi.org/10.3762/bjnano.12.24 |
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author | Awan, Uzma Azeem Raza, Abida Ali, Shaukat Saeed, Rida Fatima Akhtar, Nosheen |
author_facet | Awan, Uzma Azeem Raza, Abida Ali, Shaukat Saeed, Rida Fatima Akhtar, Nosheen |
author_sort | Awan, Uzma Azeem |
collection | PubMed |
description | Two of the limitations associated with cancer treatment are the low efficacy and the high dose-related side effects of anticancer drugs. The purpose of the current study was to fabricate biocompatible multifunctional drug-loaded nanoscale moieties for co-therapy (chemo-photothermal therapy) with maximum efficacy and minimum side effects. Herein, we report in vitro anticancerous effects of doxorubicin (DOX) loaded on gold nanorods coated with the polyelectrolyte poly(sodium-4-styrenesulfonate) (PSS-GNRs) with and without NIR laser (808 nm, power density = 1.5 W/cm(2) for 2 min) irradiation. The drug-loading capacity of PSS-GNRs was about 76% with a drug loading content of 3.2 mg DOX/mL. The cumulative DOX release significantly increased after laser exposure compared to non-irradiated samples (p < 0.05). The zeta potential values of GNRs, PSS-GNRs and DOX-PSS-GNRs were measured as 42 ± 0.1 mV, −40 ± 0.3 mV and 39.3 ± 0.6 mV, respectively. PSS-GNRs nanocomplexes were found to be biocompatible and showed higher photothermal stability. The DOX-conjugated nanocomplexes with NIR laser irradiation appear more efficient in cell inhibition (93%) than those without laser exposure (65%) and doxorubicin alone (84%). The IC(50) values of PSS-GNRs-DOX and PSS-GNRs-DOX were measured as 7.99 and 3.12 µg/mL, respectively, with laser irradiation. Thus, a combinatorial approach based on chemotherapy and photothermal strategies appears to be a promising platform in cancer management. |
format | Online Article Text |
id | pubmed-8022204 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-80222042021-05-18 Doxorubicin-loaded gold nanorods: a multifunctional chemo-photothermal nanoplatform for cancer management Awan, Uzma Azeem Raza, Abida Ali, Shaukat Saeed, Rida Fatima Akhtar, Nosheen Beilstein J Nanotechnol Full Research Paper Two of the limitations associated with cancer treatment are the low efficacy and the high dose-related side effects of anticancer drugs. The purpose of the current study was to fabricate biocompatible multifunctional drug-loaded nanoscale moieties for co-therapy (chemo-photothermal therapy) with maximum efficacy and minimum side effects. Herein, we report in vitro anticancerous effects of doxorubicin (DOX) loaded on gold nanorods coated with the polyelectrolyte poly(sodium-4-styrenesulfonate) (PSS-GNRs) with and without NIR laser (808 nm, power density = 1.5 W/cm(2) for 2 min) irradiation. The drug-loading capacity of PSS-GNRs was about 76% with a drug loading content of 3.2 mg DOX/mL. The cumulative DOX release significantly increased after laser exposure compared to non-irradiated samples (p < 0.05). The zeta potential values of GNRs, PSS-GNRs and DOX-PSS-GNRs were measured as 42 ± 0.1 mV, −40 ± 0.3 mV and 39.3 ± 0.6 mV, respectively. PSS-GNRs nanocomplexes were found to be biocompatible and showed higher photothermal stability. The DOX-conjugated nanocomplexes with NIR laser irradiation appear more efficient in cell inhibition (93%) than those without laser exposure (65%) and doxorubicin alone (84%). The IC(50) values of PSS-GNRs-DOX and PSS-GNRs-DOX were measured as 7.99 and 3.12 µg/mL, respectively, with laser irradiation. Thus, a combinatorial approach based on chemotherapy and photothermal strategies appears to be a promising platform in cancer management. Beilstein-Institut 2021-03-31 /pmc/articles/PMC8022204/ /pubmed/34012759 http://dx.doi.org/10.3762/bjnano.12.24 Text en Copyright © 2021, Awan et al. https://creativecommons.org/licenses/by/4.0https://www.beilstein-journals.org/bjnano/terms/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0). Please note that the reuse, redistribution and reproduction in particular requires that the author(s) and source are credited and that individual graphics may be subject to special legal provisions. The license is subject to the Beilstein Journal of Nanotechnology terms and conditions: (https://www.beilstein-journals.org/bjnano/terms/terms) |
spellingShingle | Full Research Paper Awan, Uzma Azeem Raza, Abida Ali, Shaukat Saeed, Rida Fatima Akhtar, Nosheen Doxorubicin-loaded gold nanorods: a multifunctional chemo-photothermal nanoplatform for cancer management |
title | Doxorubicin-loaded gold nanorods: a multifunctional chemo-photothermal nanoplatform for cancer management |
title_full | Doxorubicin-loaded gold nanorods: a multifunctional chemo-photothermal nanoplatform for cancer management |
title_fullStr | Doxorubicin-loaded gold nanorods: a multifunctional chemo-photothermal nanoplatform for cancer management |
title_full_unstemmed | Doxorubicin-loaded gold nanorods: a multifunctional chemo-photothermal nanoplatform for cancer management |
title_short | Doxorubicin-loaded gold nanorods: a multifunctional chemo-photothermal nanoplatform for cancer management |
title_sort | doxorubicin-loaded gold nanorods: a multifunctional chemo-photothermal nanoplatform for cancer management |
topic | Full Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8022204/ https://www.ncbi.nlm.nih.gov/pubmed/34012759 http://dx.doi.org/10.3762/bjnano.12.24 |
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