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Doxorubicin-conjugated PLA-PEG-Folate based polymeric micelle for tumor-targeted delivery: Synthesis and in vitro evaluation
BACKGROUND: Selective delivery of anticancer agents to target areas in the body is desirable to minimize the side effects while maximizing the therapeutic efficacy. Anthracycline antibiotics such as doxorubicin (DOX) are widely used for treatment of a wide variety of solid tumors. This study evaluat...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3996029/ https://www.ncbi.nlm.nih.gov/pubmed/24602477 http://dx.doi.org/10.1186/2008-2231-22-30 |
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author | Hami, Zahra Amini, Mohsen Ghazi-Khansari, Mahmoud Rezayat, Seyed Mehdi Gilani, Kambiz |
author_facet | Hami, Zahra Amini, Mohsen Ghazi-Khansari, Mahmoud Rezayat, Seyed Mehdi Gilani, Kambiz |
author_sort | Hami, Zahra |
collection | PubMed |
description | BACKGROUND: Selective delivery of anticancer agents to target areas in the body is desirable to minimize the side effects while maximizing the therapeutic efficacy. Anthracycline antibiotics such as doxorubicin (DOX) are widely used for treatment of a wide variety of solid tumors. This study evaluated the potential of a polymeric micellar formulation of doxorubicin as a nanocarrier system for targeted therapy of a folate-receptor positive human ovarian cancer cell in line. RESULTS: DOX-conjugated targeting and non-targeting micelles prepared by the dialysis method were about 188 and 182 nm in diameter, respectively and their critical micelle concentration was 9.55 μg/ml. The DOX-conjugated micelles exhibited a potent cytotoxicity against SKOV3 human ovarian cancer cells. Moreover, the targeting micelles showed higher cytotoxicity than that of non-targeting ones (IC(50) = 4.65 μg/ml vs 13.51 μg/ml). CONCLUSION: The prepared micelle is expected to increase the efficacy of DOX against cancer cells and reduce its side effects. |
format | Online Article Text |
id | pubmed-3996029 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-39960292014-04-24 Doxorubicin-conjugated PLA-PEG-Folate based polymeric micelle for tumor-targeted delivery: Synthesis and in vitro evaluation Hami, Zahra Amini, Mohsen Ghazi-Khansari, Mahmoud Rezayat, Seyed Mehdi Gilani, Kambiz Daru Research Article BACKGROUND: Selective delivery of anticancer agents to target areas in the body is desirable to minimize the side effects while maximizing the therapeutic efficacy. Anthracycline antibiotics such as doxorubicin (DOX) are widely used for treatment of a wide variety of solid tumors. This study evaluated the potential of a polymeric micellar formulation of doxorubicin as a nanocarrier system for targeted therapy of a folate-receptor positive human ovarian cancer cell in line. RESULTS: DOX-conjugated targeting and non-targeting micelles prepared by the dialysis method were about 188 and 182 nm in diameter, respectively and their critical micelle concentration was 9.55 μg/ml. The DOX-conjugated micelles exhibited a potent cytotoxicity against SKOV3 human ovarian cancer cells. Moreover, the targeting micelles showed higher cytotoxicity than that of non-targeting ones (IC(50) = 4.65 μg/ml vs 13.51 μg/ml). CONCLUSION: The prepared micelle is expected to increase the efficacy of DOX against cancer cells and reduce its side effects. BioMed Central 2014-03-06 /pmc/articles/PMC3996029/ /pubmed/24602477 http://dx.doi.org/10.1186/2008-2231-22-30 Text en Copyright © 2014 Hami et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Hami, Zahra Amini, Mohsen Ghazi-Khansari, Mahmoud Rezayat, Seyed Mehdi Gilani, Kambiz Doxorubicin-conjugated PLA-PEG-Folate based polymeric micelle for tumor-targeted delivery: Synthesis and in vitro evaluation |
title | Doxorubicin-conjugated PLA-PEG-Folate based polymeric micelle for tumor-targeted delivery: Synthesis and in vitro evaluation |
title_full | Doxorubicin-conjugated PLA-PEG-Folate based polymeric micelle for tumor-targeted delivery: Synthesis and in vitro evaluation |
title_fullStr | Doxorubicin-conjugated PLA-PEG-Folate based polymeric micelle for tumor-targeted delivery: Synthesis and in vitro evaluation |
title_full_unstemmed | Doxorubicin-conjugated PLA-PEG-Folate based polymeric micelle for tumor-targeted delivery: Synthesis and in vitro evaluation |
title_short | Doxorubicin-conjugated PLA-PEG-Folate based polymeric micelle for tumor-targeted delivery: Synthesis and in vitro evaluation |
title_sort | doxorubicin-conjugated pla-peg-folate based polymeric micelle for tumor-targeted delivery: synthesis and in vitro evaluation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3996029/ https://www.ncbi.nlm.nih.gov/pubmed/24602477 http://dx.doi.org/10.1186/2008-2231-22-30 |
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