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Size-Dependent Photodynamic Anticancer Activity of Biocompatible Multifunctional Magnetic Submicron Particles in Prostate Cancer Cells
In this study, newly designed biocompatible multifunctional magnetic submicron particles (CoFe(2)O(4)-HPs-FAs) of well-defined sizes (60, 133, 245, and 335 nm) were fabricated for application as a photosensitizer delivery agent for photodynamic therapy in cancer cells. To provide selective targeting...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273714/ https://www.ncbi.nlm.nih.gov/pubmed/27607999 http://dx.doi.org/10.3390/molecules21091187 |
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author | Choi, Kyong-Hoon Nam, Ki Chang Malkinski, Leszek Choi, Eun Ha Jung, Jin-Seung Park, Bong Joo |
author_facet | Choi, Kyong-Hoon Nam, Ki Chang Malkinski, Leszek Choi, Eun Ha Jung, Jin-Seung Park, Bong Joo |
author_sort | Choi, Kyong-Hoon |
collection | PubMed |
description | In this study, newly designed biocompatible multifunctional magnetic submicron particles (CoFe(2)O(4)-HPs-FAs) of well-defined sizes (60, 133, 245, and 335 nm) were fabricated for application as a photosensitizer delivery agent for photodynamic therapy in cancer cells. To provide selective targeting of cancer cells and destruction of cancer cell functionality, basic cobalt ferrite (CoFe(2)O(4)) particles were covalently bonded with a photosensitizer (PS), which comprises hematoporphyrin (HP), and folic acid (FA) molecules. The magnetic properties of the CoFe(2)O(4) particles were finely adjusted by controlling the size of the primary CoFe(2)O(4) nanograins, and secondary superstructured composite particles were formed by aggregation of the nanograins. The prepared CoFe(2)O(4)-HP-FA exhibited high water solubility, good MR-imaging capacity, and biocompatibility without any in vitro cytotoxicity. In particular, our CoFe(2)O(4)-HP-FA exhibited remarkable photodynamic anticancer efficiency via induction of apoptotic death in PC-3 prostate cancer cells in a particle size- and concentration-dependent manner. This size-dependent effect was determined by the specific surface area of the particles because the number of HP molecules increased with decreasing size and increasing surface area. These results indicate that our CoFe(2)O(4)-HP-FA may be applicable for photodynamic therapy (PDT) as a PS delivery material and a therapeutic agent for MR-imaging based PDT owing to their high saturation value for magnetization and superparamagnetism. |
format | Online Article Text |
id | pubmed-6273714 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62737142018-12-28 Size-Dependent Photodynamic Anticancer Activity of Biocompatible Multifunctional Magnetic Submicron Particles in Prostate Cancer Cells Choi, Kyong-Hoon Nam, Ki Chang Malkinski, Leszek Choi, Eun Ha Jung, Jin-Seung Park, Bong Joo Molecules Article In this study, newly designed biocompatible multifunctional magnetic submicron particles (CoFe(2)O(4)-HPs-FAs) of well-defined sizes (60, 133, 245, and 335 nm) were fabricated for application as a photosensitizer delivery agent for photodynamic therapy in cancer cells. To provide selective targeting of cancer cells and destruction of cancer cell functionality, basic cobalt ferrite (CoFe(2)O(4)) particles were covalently bonded with a photosensitizer (PS), which comprises hematoporphyrin (HP), and folic acid (FA) molecules. The magnetic properties of the CoFe(2)O(4) particles were finely adjusted by controlling the size of the primary CoFe(2)O(4) nanograins, and secondary superstructured composite particles were formed by aggregation of the nanograins. The prepared CoFe(2)O(4)-HP-FA exhibited high water solubility, good MR-imaging capacity, and biocompatibility without any in vitro cytotoxicity. In particular, our CoFe(2)O(4)-HP-FA exhibited remarkable photodynamic anticancer efficiency via induction of apoptotic death in PC-3 prostate cancer cells in a particle size- and concentration-dependent manner. This size-dependent effect was determined by the specific surface area of the particles because the number of HP molecules increased with decreasing size and increasing surface area. These results indicate that our CoFe(2)O(4)-HP-FA may be applicable for photodynamic therapy (PDT) as a PS delivery material and a therapeutic agent for MR-imaging based PDT owing to their high saturation value for magnetization and superparamagnetism. MDPI 2016-09-06 /pmc/articles/PMC6273714/ /pubmed/27607999 http://dx.doi.org/10.3390/molecules21091187 Text en © 2016 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Choi, Kyong-Hoon Nam, Ki Chang Malkinski, Leszek Choi, Eun Ha Jung, Jin-Seung Park, Bong Joo Size-Dependent Photodynamic Anticancer Activity of Biocompatible Multifunctional Magnetic Submicron Particles in Prostate Cancer Cells |
title | Size-Dependent Photodynamic Anticancer Activity of Biocompatible Multifunctional Magnetic Submicron Particles in Prostate Cancer Cells |
title_full | Size-Dependent Photodynamic Anticancer Activity of Biocompatible Multifunctional Magnetic Submicron Particles in Prostate Cancer Cells |
title_fullStr | Size-Dependent Photodynamic Anticancer Activity of Biocompatible Multifunctional Magnetic Submicron Particles in Prostate Cancer Cells |
title_full_unstemmed | Size-Dependent Photodynamic Anticancer Activity of Biocompatible Multifunctional Magnetic Submicron Particles in Prostate Cancer Cells |
title_short | Size-Dependent Photodynamic Anticancer Activity of Biocompatible Multifunctional Magnetic Submicron Particles in Prostate Cancer Cells |
title_sort | size-dependent photodynamic anticancer activity of biocompatible multifunctional magnetic submicron particles in prostate cancer cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273714/ https://www.ncbi.nlm.nih.gov/pubmed/27607999 http://dx.doi.org/10.3390/molecules21091187 |
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