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Target delivery of doxorubicin tethered with PVP stabilized gold nanoparticles for effective treatment of lung cancer

Development of drug delivery system conjugated with doxorubicin (dox) on the surface of AuNPs with polyvinylpyrrolidone (Dox@PVP-AuNPs), we have demonstrated that human lung cancer cells can significantly overcome by the combination of highly effective cellular entry and responsive intracellular rel...

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Autores principales: Ramalingam, Vaikundamoorthy, Varunkumar, Krishnamoorthy, Ravikumar, Vilwanathan, Rajaram, Rajendran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5830607/
https://www.ncbi.nlm.nih.gov/pubmed/29491463
http://dx.doi.org/10.1038/s41598-018-22172-5
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author Ramalingam, Vaikundamoorthy
Varunkumar, Krishnamoorthy
Ravikumar, Vilwanathan
Rajaram, Rajendran
author_facet Ramalingam, Vaikundamoorthy
Varunkumar, Krishnamoorthy
Ravikumar, Vilwanathan
Rajaram, Rajendran
author_sort Ramalingam, Vaikundamoorthy
collection PubMed
description Development of drug delivery system conjugated with doxorubicin (dox) on the surface of AuNPs with polyvinylpyrrolidone (Dox@PVP-AuNPs), we have demonstrated that human lung cancer cells can significantly overcome by the combination of highly effective cellular entry and responsive intracellular release of doxorubicin from Dox@PVP-AuNPs complex. Previously drug release from doxorubicin-conjugated AuNPs was confirmed by the recovered fluorescence of doxorubicin from quenching due to the nanosurface energy transfer between doxorubicinyl groups and AuNPs. Dox@PVP-AuNPs achieved enhanced inhibition of lung cancer cells growth than free Doxorubicin and PVP-AuNPs. The in vitro cytotoxic effect of PVP-AuNPs, free Dox and Dox@PVP-AuNPs inhibited the proliferation of human lung cancer cells with IC(50) concentration. Compared with control cells, PVP-AuNPs and free Dox, Dox@PVP-AuNPs can increases ROS generation, sensitize mitochondrial membrane potential and induces both early and late apoptosis in lung cancer cells. Moreover, Dox@PVP-AuNPs highly upregulates the expression of tumor suppressor genes than free Dox and PVP-AuNPs and induces intrinsic apoptosis in lung cancer cells. From the results, Dox@PVP-AuNPs can be considered as an potential drug delivery system for effective treatment of human lung cancer.
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spelling pubmed-58306072018-03-05 Target delivery of doxorubicin tethered with PVP stabilized gold nanoparticles for effective treatment of lung cancer Ramalingam, Vaikundamoorthy Varunkumar, Krishnamoorthy Ravikumar, Vilwanathan Rajaram, Rajendran Sci Rep Article Development of drug delivery system conjugated with doxorubicin (dox) on the surface of AuNPs with polyvinylpyrrolidone (Dox@PVP-AuNPs), we have demonstrated that human lung cancer cells can significantly overcome by the combination of highly effective cellular entry and responsive intracellular release of doxorubicin from Dox@PVP-AuNPs complex. Previously drug release from doxorubicin-conjugated AuNPs was confirmed by the recovered fluorescence of doxorubicin from quenching due to the nanosurface energy transfer between doxorubicinyl groups and AuNPs. Dox@PVP-AuNPs achieved enhanced inhibition of lung cancer cells growth than free Doxorubicin and PVP-AuNPs. The in vitro cytotoxic effect of PVP-AuNPs, free Dox and Dox@PVP-AuNPs inhibited the proliferation of human lung cancer cells with IC(50) concentration. Compared with control cells, PVP-AuNPs and free Dox, Dox@PVP-AuNPs can increases ROS generation, sensitize mitochondrial membrane potential and induces both early and late apoptosis in lung cancer cells. Moreover, Dox@PVP-AuNPs highly upregulates the expression of tumor suppressor genes than free Dox and PVP-AuNPs and induces intrinsic apoptosis in lung cancer cells. From the results, Dox@PVP-AuNPs can be considered as an potential drug delivery system for effective treatment of human lung cancer. Nature Publishing Group UK 2018-02-28 /pmc/articles/PMC5830607/ /pubmed/29491463 http://dx.doi.org/10.1038/s41598-018-22172-5 Text en © The Author(s) 2018 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Ramalingam, Vaikundamoorthy
Varunkumar, Krishnamoorthy
Ravikumar, Vilwanathan
Rajaram, Rajendran
Target delivery of doxorubicin tethered with PVP stabilized gold nanoparticles for effective treatment of lung cancer
title Target delivery of doxorubicin tethered with PVP stabilized gold nanoparticles for effective treatment of lung cancer
title_full Target delivery of doxorubicin tethered with PVP stabilized gold nanoparticles for effective treatment of lung cancer
title_fullStr Target delivery of doxorubicin tethered with PVP stabilized gold nanoparticles for effective treatment of lung cancer
title_full_unstemmed Target delivery of doxorubicin tethered with PVP stabilized gold nanoparticles for effective treatment of lung cancer
title_short Target delivery of doxorubicin tethered with PVP stabilized gold nanoparticles for effective treatment of lung cancer
title_sort target delivery of doxorubicin tethered with pvp stabilized gold nanoparticles for effective treatment of lung cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5830607/
https://www.ncbi.nlm.nih.gov/pubmed/29491463
http://dx.doi.org/10.1038/s41598-018-22172-5
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