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Magnetic liposomes for colorectal cancer cells therapy by high-frequency magnetic field treatment

In this study, we developed the cancer treatment through the combination of chemotherapy and thermotherapy using doxorubicin-loaded magnetic liposomes. The citric acid-coated magnetic nanoparticles (CAMNP, ca. 10 nm) and doxorubicin were encapsulated into the liposome (HSPC/DSPE/cholesterol = 12.5:1...

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Autores principales: Hardiansyah, Andri, Huang, Li-Ying, Yang, Ming-Chien, Liu, Ting-Yu, Tsai, Sung-Chen, Yang, Chih-Yung, Kuo, Chih-Yu, Chan, Tzu-Yi, Zou, Hui-Ming, Lian, Wei-Nan, Lin, Chi-Hung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4169134/
https://www.ncbi.nlm.nih.gov/pubmed/25246875
http://dx.doi.org/10.1186/1556-276X-9-497
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author Hardiansyah, Andri
Huang, Li-Ying
Yang, Ming-Chien
Liu, Ting-Yu
Tsai, Sung-Chen
Yang, Chih-Yung
Kuo, Chih-Yu
Chan, Tzu-Yi
Zou, Hui-Ming
Lian, Wei-Nan
Lin, Chi-Hung
author_facet Hardiansyah, Andri
Huang, Li-Ying
Yang, Ming-Chien
Liu, Ting-Yu
Tsai, Sung-Chen
Yang, Chih-Yung
Kuo, Chih-Yu
Chan, Tzu-Yi
Zou, Hui-Ming
Lian, Wei-Nan
Lin, Chi-Hung
author_sort Hardiansyah, Andri
collection PubMed
description In this study, we developed the cancer treatment through the combination of chemotherapy and thermotherapy using doxorubicin-loaded magnetic liposomes. The citric acid-coated magnetic nanoparticles (CAMNP, ca. 10 nm) and doxorubicin were encapsulated into the liposome (HSPC/DSPE/cholesterol = 12.5:1:8.25) by rotary evaporation and ultrasonication process. The resultant magnetic liposomes (ca. 90 to 130 nm) were subject to characterization including transmission electron microscopy (TEM), dynamic light scattering (DLS), X-ray diffraction (XRD), zeta potential, Fourier transform infrared (FTIR) spectrophotometer, and fluorescence microscope. In vitro cytotoxicity of the drug carrier platform was investigated through 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay using L-929 cells, as the mammalian cell model. In vitro cytotoxicity and hyperthermia (inductive heating) studies were evaluated against colorectal cancer (CT-26 cells) with high-frequency magnetic field (HFMF) exposure. MTT assay revealed that these drug carriers exhibited no cytotoxicity against L-929 cells, suggesting excellent biocompatibility. When the magnetic liposomes with 1 μM doxorubicin was used to treat CT-26 cells in combination with HFMF exposure, approximately 56% cells were killed and found to be more effective than either hyperthermia or chemotherapy treatment individually. Therefore, these results show that the synergistic effects between chemotherapy (drug-controlled release) and hyperthermia increase the capability to kill cancer cells.
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spelling pubmed-41691342014-09-22 Magnetic liposomes for colorectal cancer cells therapy by high-frequency magnetic field treatment Hardiansyah, Andri Huang, Li-Ying Yang, Ming-Chien Liu, Ting-Yu Tsai, Sung-Chen Yang, Chih-Yung Kuo, Chih-Yu Chan, Tzu-Yi Zou, Hui-Ming Lian, Wei-Nan Lin, Chi-Hung Nanoscale Res Lett Nano Express In this study, we developed the cancer treatment through the combination of chemotherapy and thermotherapy using doxorubicin-loaded magnetic liposomes. The citric acid-coated magnetic nanoparticles (CAMNP, ca. 10 nm) and doxorubicin were encapsulated into the liposome (HSPC/DSPE/cholesterol = 12.5:1:8.25) by rotary evaporation and ultrasonication process. The resultant magnetic liposomes (ca. 90 to 130 nm) were subject to characterization including transmission electron microscopy (TEM), dynamic light scattering (DLS), X-ray diffraction (XRD), zeta potential, Fourier transform infrared (FTIR) spectrophotometer, and fluorescence microscope. In vitro cytotoxicity of the drug carrier platform was investigated through 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay using L-929 cells, as the mammalian cell model. In vitro cytotoxicity and hyperthermia (inductive heating) studies were evaluated against colorectal cancer (CT-26 cells) with high-frequency magnetic field (HFMF) exposure. MTT assay revealed that these drug carriers exhibited no cytotoxicity against L-929 cells, suggesting excellent biocompatibility. When the magnetic liposomes with 1 μM doxorubicin was used to treat CT-26 cells in combination with HFMF exposure, approximately 56% cells were killed and found to be more effective than either hyperthermia or chemotherapy treatment individually. Therefore, these results show that the synergistic effects between chemotherapy (drug-controlled release) and hyperthermia increase the capability to kill cancer cells. Springer 2014-09-15 /pmc/articles/PMC4169134/ /pubmed/25246875 http://dx.doi.org/10.1186/1556-276X-9-497 Text en Copyright © 2014 Hardiansyah et al.; licensee Springer. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited.
spellingShingle Nano Express
Hardiansyah, Andri
Huang, Li-Ying
Yang, Ming-Chien
Liu, Ting-Yu
Tsai, Sung-Chen
Yang, Chih-Yung
Kuo, Chih-Yu
Chan, Tzu-Yi
Zou, Hui-Ming
Lian, Wei-Nan
Lin, Chi-Hung
Magnetic liposomes for colorectal cancer cells therapy by high-frequency magnetic field treatment
title Magnetic liposomes for colorectal cancer cells therapy by high-frequency magnetic field treatment
title_full Magnetic liposomes for colorectal cancer cells therapy by high-frequency magnetic field treatment
title_fullStr Magnetic liposomes for colorectal cancer cells therapy by high-frequency magnetic field treatment
title_full_unstemmed Magnetic liposomes for colorectal cancer cells therapy by high-frequency magnetic field treatment
title_short Magnetic liposomes for colorectal cancer cells therapy by high-frequency magnetic field treatment
title_sort magnetic liposomes for colorectal cancer cells therapy by high-frequency magnetic field treatment
topic Nano Express
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4169134/
https://www.ncbi.nlm.nih.gov/pubmed/25246875
http://dx.doi.org/10.1186/1556-276X-9-497
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