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Development and Characterization of Novel LipoCEST Agents Based on Thermosensitive Liposomes
PURPOSE: To develop a novel probe for chemical exchange saturation transfer magnetic resonance imaging (CEST MRI) based on thermosensitive liposomes (lipoCEST) for theranostics, in which diagnostics and therapy are integrated into a single platform. METHODS: We developed two kinds of lipoCEST agents...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Japanese Society for Magnetic Resonance in Medicine
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5608129/ https://www.ncbi.nlm.nih.gov/pubmed/26841852 http://dx.doi.org/10.2463/mrms.mp.2015-0039 |
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author | MARUYAMA, Shuki UEDA, Junpei KIMURA, Atsuomi MURASE, Kenya |
author_facet | MARUYAMA, Shuki UEDA, Junpei KIMURA, Atsuomi MURASE, Kenya |
author_sort | MARUYAMA, Shuki |
collection | PubMed |
description | PURPOSE: To develop a novel probe for chemical exchange saturation transfer magnetic resonance imaging (CEST MRI) based on thermosensitive liposomes (lipoCEST) for theranostics, in which diagnostics and therapy are integrated into a single platform. METHODS: We developed two kinds of lipoCEST agents. The first kind encapsulated dysprosium (Dy)-1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid (DOTA)-Na·3NaCl, terbium-DOTA-Na·3NaCl, or thulium-DOTA-Na·3NaCl into the inner cavity of thermosensitive liposomes, while the second kind encapsulated Dy-DOTA-Na and incorporated amphiphilic metal complex [thulium-diethylenetriamine pentaacetic acid-bis (stearylamide) (Tm-DTPA-BSA)] as a membrane constituent. The nuclear magnetic resonance (NMR)- and Z-spectra of these lipoCEST agents were acquired at various temperatures on a 9.4T MRI scanner. To investigate their applicability to the drug release induced by hyperthermia, we also encapsulated a fluorescent dye (calcein) into the inner cavity of liposomes and measured calcein release after warming them. RESULTS: The intra- and extraliposomal water signals could be differentiated in all agents from their NMR- and Z-spectra. The agent incorporating Tm-DTPA-BSA showed the largest chemical shift (approximately 15 ppm) derived from the intraliposomal water protons. The calcein retained in this agent was successfully released at 44°C. The agent incorporating 30 mol% of Tm-DTPA-BSA in its membrane released more calcein at 42–44°C than that of the agent incorporating 10 mol%. CONCLUSION: We developed novel thermosensitive lipoCEST agents and characterized them. Our preliminary results suggest that they are useful and can be applied to theranostics. |
format | Online Article Text |
id | pubmed-5608129 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Japanese Society for Magnetic Resonance in Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-56081292017-10-23 Development and Characterization of Novel LipoCEST Agents Based on Thermosensitive Liposomes MARUYAMA, Shuki UEDA, Junpei KIMURA, Atsuomi MURASE, Kenya Magn Reson Med Sci Major Paper PURPOSE: To develop a novel probe for chemical exchange saturation transfer magnetic resonance imaging (CEST MRI) based on thermosensitive liposomes (lipoCEST) for theranostics, in which diagnostics and therapy are integrated into a single platform. METHODS: We developed two kinds of lipoCEST agents. The first kind encapsulated dysprosium (Dy)-1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid (DOTA)-Na·3NaCl, terbium-DOTA-Na·3NaCl, or thulium-DOTA-Na·3NaCl into the inner cavity of thermosensitive liposomes, while the second kind encapsulated Dy-DOTA-Na and incorporated amphiphilic metal complex [thulium-diethylenetriamine pentaacetic acid-bis (stearylamide) (Tm-DTPA-BSA)] as a membrane constituent. The nuclear magnetic resonance (NMR)- and Z-spectra of these lipoCEST agents were acquired at various temperatures on a 9.4T MRI scanner. To investigate their applicability to the drug release induced by hyperthermia, we also encapsulated a fluorescent dye (calcein) into the inner cavity of liposomes and measured calcein release after warming them. RESULTS: The intra- and extraliposomal water signals could be differentiated in all agents from their NMR- and Z-spectra. The agent incorporating Tm-DTPA-BSA showed the largest chemical shift (approximately 15 ppm) derived from the intraliposomal water protons. The calcein retained in this agent was successfully released at 44°C. The agent incorporating 30 mol% of Tm-DTPA-BSA in its membrane released more calcein at 42–44°C than that of the agent incorporating 10 mol%. CONCLUSION: We developed novel thermosensitive lipoCEST agents and characterized them. Our preliminary results suggest that they are useful and can be applied to theranostics. Japanese Society for Magnetic Resonance in Medicine 2016-02-03 /pmc/articles/PMC5608129/ /pubmed/26841852 http://dx.doi.org/10.2463/mrms.mp.2015-0039 Text en © 2016 Japanese Society for Magnetic Resonance in Medicine http://creativecommons.org/licenses/by/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives International License. |
spellingShingle | Major Paper MARUYAMA, Shuki UEDA, Junpei KIMURA, Atsuomi MURASE, Kenya Development and Characterization of Novel LipoCEST Agents Based on Thermosensitive Liposomes |
title | Development and Characterization of Novel LipoCEST Agents Based on Thermosensitive Liposomes |
title_full | Development and Characterization of Novel LipoCEST Agents Based on Thermosensitive Liposomes |
title_fullStr | Development and Characterization of Novel LipoCEST Agents Based on Thermosensitive Liposomes |
title_full_unstemmed | Development and Characterization of Novel LipoCEST Agents Based on Thermosensitive Liposomes |
title_short | Development and Characterization of Novel LipoCEST Agents Based on Thermosensitive Liposomes |
title_sort | development and characterization of novel lipocest agents based on thermosensitive liposomes |
topic | Major Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5608129/ https://www.ncbi.nlm.nih.gov/pubmed/26841852 http://dx.doi.org/10.2463/mrms.mp.2015-0039 |
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