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Enhanced tumor targeting effects of a novel paclitaxel-loaded polymer: PEG–PCCL-modified magnetic iron oxide nanoparticles
Background: Multifunctional magnetic nanoparticles (MNP) have been newly developed for tumor-targeted drug carriers. To address challenges including biocompatibility, stability, nontoxicity, and targeting efficiency, here we report the novel drug deliverer poly(ethylene glycol) carboxyl–poly(ɛ-capro...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8241137/ https://www.ncbi.nlm.nih.gov/pubmed/28891337 http://dx.doi.org/10.1080/10717544.2017.1373167 |
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author | Li, Xinyi Yang, Yuan Jia, Yiping Pu, Xuan Yang, Ting Wang, Yicheng Ma, Xuefei Chen, Qi Sun, Mengwen Wei, Dapeng Kuang, Yu Li, Yang Liu, Yu |
author_facet | Li, Xinyi Yang, Yuan Jia, Yiping Pu, Xuan Yang, Ting Wang, Yicheng Ma, Xuefei Chen, Qi Sun, Mengwen Wei, Dapeng Kuang, Yu Li, Yang Liu, Yu |
author_sort | Li, Xinyi |
collection | PubMed |
description | Background: Multifunctional magnetic nanoparticles (MNP) have been newly developed for tumor-targeted drug carriers. To address challenges including biocompatibility, stability, nontoxicity, and targeting efficiency, here we report the novel drug deliverer poly(ethylene glycol) carboxyl–poly(ɛ-caprolactone) modified MNP (PEG–PCCL-MNP) suitable for magnetic targeting based on our previous studies. Methods: Their in vitro characterization and cytotoxicity assessments, in vivo cytotoxicity assessments, and antitumor efficacy study were elaborately investigated. Results: The size of PEG–PCCL-MNP was 79.6 ± 0.945 nm. PEG–PCCL-MNP showed little in vitro or in vivo cytotoxicity and good biocompatibility, as well as effective tumor-specific cell targeting for drug delivery with the presence of external magnetic field. Discussion: PEG–PCCL-MNP is a potential candidate of biocompatible and tumor-specific targeting drug vehicle for hydrophobic drugs. |
format | Online Article Text |
id | pubmed-8241137 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-82411372021-07-08 Enhanced tumor targeting effects of a novel paclitaxel-loaded polymer: PEG–PCCL-modified magnetic iron oxide nanoparticles Li, Xinyi Yang, Yuan Jia, Yiping Pu, Xuan Yang, Ting Wang, Yicheng Ma, Xuefei Chen, Qi Sun, Mengwen Wei, Dapeng Kuang, Yu Li, Yang Liu, Yu Drug Deliv Research Article Background: Multifunctional magnetic nanoparticles (MNP) have been newly developed for tumor-targeted drug carriers. To address challenges including biocompatibility, stability, nontoxicity, and targeting efficiency, here we report the novel drug deliverer poly(ethylene glycol) carboxyl–poly(ɛ-caprolactone) modified MNP (PEG–PCCL-MNP) suitable for magnetic targeting based on our previous studies. Methods: Their in vitro characterization and cytotoxicity assessments, in vivo cytotoxicity assessments, and antitumor efficacy study were elaborately investigated. Results: The size of PEG–PCCL-MNP was 79.6 ± 0.945 nm. PEG–PCCL-MNP showed little in vitro or in vivo cytotoxicity and good biocompatibility, as well as effective tumor-specific cell targeting for drug delivery with the presence of external magnetic field. Discussion: PEG–PCCL-MNP is a potential candidate of biocompatible and tumor-specific targeting drug vehicle for hydrophobic drugs. Taylor & Francis 2017-09-11 /pmc/articles/PMC8241137/ /pubmed/28891337 http://dx.doi.org/10.1080/10717544.2017.1373167 Text en © 2017 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Li, Xinyi Yang, Yuan Jia, Yiping Pu, Xuan Yang, Ting Wang, Yicheng Ma, Xuefei Chen, Qi Sun, Mengwen Wei, Dapeng Kuang, Yu Li, Yang Liu, Yu Enhanced tumor targeting effects of a novel paclitaxel-loaded polymer: PEG–PCCL-modified magnetic iron oxide nanoparticles |
title | Enhanced tumor targeting effects of a novel paclitaxel-loaded polymer: PEG–PCCL-modified magnetic iron oxide nanoparticles |
title_full | Enhanced tumor targeting effects of a novel paclitaxel-loaded polymer: PEG–PCCL-modified magnetic iron oxide nanoparticles |
title_fullStr | Enhanced tumor targeting effects of a novel paclitaxel-loaded polymer: PEG–PCCL-modified magnetic iron oxide nanoparticles |
title_full_unstemmed | Enhanced tumor targeting effects of a novel paclitaxel-loaded polymer: PEG–PCCL-modified magnetic iron oxide nanoparticles |
title_short | Enhanced tumor targeting effects of a novel paclitaxel-loaded polymer: PEG–PCCL-modified magnetic iron oxide nanoparticles |
title_sort | enhanced tumor targeting effects of a novel paclitaxel-loaded polymer: peg–pccl-modified magnetic iron oxide nanoparticles |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8241137/ https://www.ncbi.nlm.nih.gov/pubmed/28891337 http://dx.doi.org/10.1080/10717544.2017.1373167 |
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