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Metallo-Curcumin-Conjugated DNA Complexes Induces Preferential Prostate Cancer Cells Cytotoxicity and Pause Growth of Bacterial Cells
DNA nanotechnology can be used to create intricate DNA structures due to the ability to direct the molecular assembly of nanostructures through a bottom-up approach. Here, we propose nanocarriers composed of both synthetic and natural DNA for drug delivery. The topological, optical characteristics,...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6175843/ https://www.ncbi.nlm.nih.gov/pubmed/30297802 http://dx.doi.org/10.1038/s41598-018-33369-z |
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author | Vellampatti, Srivithya Chandrasekaran, Gopalakrishnan Mitta, Sekhar Babu Lakshmanan, Vinoth-Kumar Park, Sung Ha |
author_facet | Vellampatti, Srivithya Chandrasekaran, Gopalakrishnan Mitta, Sekhar Babu Lakshmanan, Vinoth-Kumar Park, Sung Ha |
author_sort | Vellampatti, Srivithya |
collection | PubMed |
description | DNA nanotechnology can be used to create intricate DNA structures due to the ability to direct the molecular assembly of nanostructures through a bottom-up approach. Here, we propose nanocarriers composed of both synthetic and natural DNA for drug delivery. The topological, optical characteristics, and interaction studies of Cu(2+)/Ni(2+)/Zn(2+)-curcumin-conjugated DNA complexes were studied using atomic force microscopy (AFM), UV-vis spectroscopy, Fourier transform infrared and mass spectroscopy. The maximum release of metallo-curcumin conjugates from the DNA complexes, triggered by switching the pH, was found in an acidic medium. The bacterial growth curves of E. coli and B. subtilis displayed a prolonged lag phase when tested with the metallo-curcumin-conjugated DNA complexes. We also tested the in vitro cytotoxicity of the metallo-curcumin-conjugated DNA complexes to prostate cancer cells using an MTS assay, which indicated potent growth inhibition of the cells. Finally, we studied the cellular uptake of the complexes, revealing that DNA complexes with Cu(2+)/Ni(2+)-curcumin exhibited brighter fluorescence than those with Zn(2+)-curcumin. |
format | Online Article Text |
id | pubmed-6175843 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-61758432018-10-12 Metallo-Curcumin-Conjugated DNA Complexes Induces Preferential Prostate Cancer Cells Cytotoxicity and Pause Growth of Bacterial Cells Vellampatti, Srivithya Chandrasekaran, Gopalakrishnan Mitta, Sekhar Babu Lakshmanan, Vinoth-Kumar Park, Sung Ha Sci Rep Article DNA nanotechnology can be used to create intricate DNA structures due to the ability to direct the molecular assembly of nanostructures through a bottom-up approach. Here, we propose nanocarriers composed of both synthetic and natural DNA for drug delivery. The topological, optical characteristics, and interaction studies of Cu(2+)/Ni(2+)/Zn(2+)-curcumin-conjugated DNA complexes were studied using atomic force microscopy (AFM), UV-vis spectroscopy, Fourier transform infrared and mass spectroscopy. The maximum release of metallo-curcumin conjugates from the DNA complexes, triggered by switching the pH, was found in an acidic medium. The bacterial growth curves of E. coli and B. subtilis displayed a prolonged lag phase when tested with the metallo-curcumin-conjugated DNA complexes. We also tested the in vitro cytotoxicity of the metallo-curcumin-conjugated DNA complexes to prostate cancer cells using an MTS assay, which indicated potent growth inhibition of the cells. Finally, we studied the cellular uptake of the complexes, revealing that DNA complexes with Cu(2+)/Ni(2+)-curcumin exhibited brighter fluorescence than those with Zn(2+)-curcumin. Nature Publishing Group UK 2018-10-08 /pmc/articles/PMC6175843/ /pubmed/30297802 http://dx.doi.org/10.1038/s41598-018-33369-z 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 Vellampatti, Srivithya Chandrasekaran, Gopalakrishnan Mitta, Sekhar Babu Lakshmanan, Vinoth-Kumar Park, Sung Ha Metallo-Curcumin-Conjugated DNA Complexes Induces Preferential Prostate Cancer Cells Cytotoxicity and Pause Growth of Bacterial Cells |
title | Metallo-Curcumin-Conjugated DNA Complexes Induces Preferential Prostate Cancer Cells Cytotoxicity and Pause Growth of Bacterial Cells |
title_full | Metallo-Curcumin-Conjugated DNA Complexes Induces Preferential Prostate Cancer Cells Cytotoxicity and Pause Growth of Bacterial Cells |
title_fullStr | Metallo-Curcumin-Conjugated DNA Complexes Induces Preferential Prostate Cancer Cells Cytotoxicity and Pause Growth of Bacterial Cells |
title_full_unstemmed | Metallo-Curcumin-Conjugated DNA Complexes Induces Preferential Prostate Cancer Cells Cytotoxicity and Pause Growth of Bacterial Cells |
title_short | Metallo-Curcumin-Conjugated DNA Complexes Induces Preferential Prostate Cancer Cells Cytotoxicity and Pause Growth of Bacterial Cells |
title_sort | metallo-curcumin-conjugated dna complexes induces preferential prostate cancer cells cytotoxicity and pause growth of bacterial cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6175843/ https://www.ncbi.nlm.nih.gov/pubmed/30297802 http://dx.doi.org/10.1038/s41598-018-33369-z |
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