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In situ self-assembly of amphiphilic dextran micelles and superparamagnetic iron oxide nanoparticle-loading as magnetic resonance imaging contrast agents
Polymeric micelles have long been considered as promising nanocarrier for hydrophobic drugs and imaging probes, due to their nanoscale particle size, biocompatibility and ability to loading reasonable amount of cargoes. Herein, a facile method for dextran micelles preparation was developed and their...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9847518/ https://www.ncbi.nlm.nih.gov/pubmed/36683738 http://dx.doi.org/10.1093/rb/rbac096 |
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author | Jiang, Linrui Zheng, Rong Zeng, Ni Wu, Changqiang Su, Hongying |
author_facet | Jiang, Linrui Zheng, Rong Zeng, Ni Wu, Changqiang Su, Hongying |
author_sort | Jiang, Linrui |
collection | PubMed |
description | Polymeric micelles have long been considered as promising nanocarrier for hydrophobic drugs and imaging probes, due to their nanoscale particle size, biocompatibility and ability to loading reasonable amount of cargoes. Herein, a facile method for dextran micelles preparation was developed and their performance as carriers of superparamagnetic iron oxide (SPIO) nanocrystals was evaluated. Amphiphilic dextran (Dex-g-OA) was synthesized via the Schiff base reactions between oxidized dextran and oleylamine, and self-assembled in situ into nano-size micelles in the reaction systems. The self-assembling behaviors of the amphiphilic dextran were identified using fluorescence resonance energy transfer technique by detection the energy transfer signal between the fluorophore pairs, Cy5 and Cy5.5. Hydrophobic SPIO nanoparticles (Fe(3)O(4) NPs) were successfully loaded into the dextran micelles via the in situ self-assembly process, leading to a series of Fe(3)O(4) NPs-loaded micelle nanocomposites (Fe(3)O(4)@Dex-g-OA) with good biocompatibility, superparamagnetism and strongly enhanced T(2) relaxivity. At the magnetic field of 0.5 T, the Fe(3)O(4)@Dex-g-OA nanocomposite with particle size of 116.2 ± 53.7 nm presented a higher T(2) relaxivity of 327.9 [Formula: see text] ·s(−1). The prepared magnetic nanocomposites hold the promise to be used as contrast agents in magnetic resonance imaging. |
format | Online Article Text |
id | pubmed-9847518 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-98475182023-01-20 In situ self-assembly of amphiphilic dextran micelles and superparamagnetic iron oxide nanoparticle-loading as magnetic resonance imaging contrast agents Jiang, Linrui Zheng, Rong Zeng, Ni Wu, Changqiang Su, Hongying Regen Biomater Research Article Polymeric micelles have long been considered as promising nanocarrier for hydrophobic drugs and imaging probes, due to their nanoscale particle size, biocompatibility and ability to loading reasonable amount of cargoes. Herein, a facile method for dextran micelles preparation was developed and their performance as carriers of superparamagnetic iron oxide (SPIO) nanocrystals was evaluated. Amphiphilic dextran (Dex-g-OA) was synthesized via the Schiff base reactions between oxidized dextran and oleylamine, and self-assembled in situ into nano-size micelles in the reaction systems. The self-assembling behaviors of the amphiphilic dextran were identified using fluorescence resonance energy transfer technique by detection the energy transfer signal between the fluorophore pairs, Cy5 and Cy5.5. Hydrophobic SPIO nanoparticles (Fe(3)O(4) NPs) were successfully loaded into the dextran micelles via the in situ self-assembly process, leading to a series of Fe(3)O(4) NPs-loaded micelle nanocomposites (Fe(3)O(4)@Dex-g-OA) with good biocompatibility, superparamagnetism and strongly enhanced T(2) relaxivity. At the magnetic field of 0.5 T, the Fe(3)O(4)@Dex-g-OA nanocomposite with particle size of 116.2 ± 53.7 nm presented a higher T(2) relaxivity of 327.9 [Formula: see text] ·s(−1). The prepared magnetic nanocomposites hold the promise to be used as contrast agents in magnetic resonance imaging. Oxford University Press 2022-12-05 /pmc/articles/PMC9847518/ /pubmed/36683738 http://dx.doi.org/10.1093/rb/rbac096 Text en © The Author(s) 2022. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Jiang, Linrui Zheng, Rong Zeng, Ni Wu, Changqiang Su, Hongying In situ self-assembly of amphiphilic dextran micelles and superparamagnetic iron oxide nanoparticle-loading as magnetic resonance imaging contrast agents |
title |
In situ self-assembly of amphiphilic dextran micelles and superparamagnetic iron oxide nanoparticle-loading as magnetic resonance imaging contrast agents |
title_full |
In situ self-assembly of amphiphilic dextran micelles and superparamagnetic iron oxide nanoparticle-loading as magnetic resonance imaging contrast agents |
title_fullStr |
In situ self-assembly of amphiphilic dextran micelles and superparamagnetic iron oxide nanoparticle-loading as magnetic resonance imaging contrast agents |
title_full_unstemmed |
In situ self-assembly of amphiphilic dextran micelles and superparamagnetic iron oxide nanoparticle-loading as magnetic resonance imaging contrast agents |
title_short |
In situ self-assembly of amphiphilic dextran micelles and superparamagnetic iron oxide nanoparticle-loading as magnetic resonance imaging contrast agents |
title_sort | in situ self-assembly of amphiphilic dextran micelles and superparamagnetic iron oxide nanoparticle-loading as magnetic resonance imaging contrast agents |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9847518/ https://www.ncbi.nlm.nih.gov/pubmed/36683738 http://dx.doi.org/10.1093/rb/rbac096 |
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