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Utilization of H-bond interaction of nucleobase Uralic with antitumor methotrexate to design drug carrier with ultrahigh loading efficiency and pH-responsive drug release
A novel Uralic (U)-rich linear-hyperbranched mono-methoxy poly (ethylene glycol)-hyperbranched polyglycerol-graft-Uralic (mPEG-HPG-g-U) nanoparticle (NP) was prepared as drug carrier for antitumor methotrexate (MTX). Due to the H-bond interaction of U with MTX and hydrophobic interaction, this NP ex...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4669001/ https://www.ncbi.nlm.nih.gov/pubmed/26816622 http://dx.doi.org/10.1093/rb/rbu010 |
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author | Cai, Teng-Teng Lei, Qi Yang, Bin Jia, Hui-Zhen Cheng, Hong Liu, Li-Han Zeng, Xuan Feng, Jun Zhuo, Ren-Xi Zhang, Xian-Zheng |
author_facet | Cai, Teng-Teng Lei, Qi Yang, Bin Jia, Hui-Zhen Cheng, Hong Liu, Li-Han Zeng, Xuan Feng, Jun Zhuo, Ren-Xi Zhang, Xian-Zheng |
author_sort | Cai, Teng-Teng |
collection | PubMed |
description | A novel Uralic (U)-rich linear-hyperbranched mono-methoxy poly (ethylene glycol)-hyperbranched polyglycerol-graft-Uralic (mPEG-HPG-g-U) nanoparticle (NP) was prepared as drug carrier for antitumor methotrexate (MTX). Due to the H-bond interaction of U with MTX and hydrophobic interaction, this NP exhibited high drug loading efficiency of up to 40%, which was significantly higher than that of traditional NPs based on U-absent copolymers (<15%). In addition, MTX-loaded mPEG-HPG-g-U NPs also demonstrated an acidity-accelerated drug release behavior. |
format | Online Article Text |
id | pubmed-4669001 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-46690012016-01-26 Utilization of H-bond interaction of nucleobase Uralic with antitumor methotrexate to design drug carrier with ultrahigh loading efficiency and pH-responsive drug release Cai, Teng-Teng Lei, Qi Yang, Bin Jia, Hui-Zhen Cheng, Hong Liu, Li-Han Zeng, Xuan Feng, Jun Zhuo, Ren-Xi Zhang, Xian-Zheng Regen Biomater Research Articles A novel Uralic (U)-rich linear-hyperbranched mono-methoxy poly (ethylene glycol)-hyperbranched polyglycerol-graft-Uralic (mPEG-HPG-g-U) nanoparticle (NP) was prepared as drug carrier for antitumor methotrexate (MTX). Due to the H-bond interaction of U with MTX and hydrophobic interaction, this NP exhibited high drug loading efficiency of up to 40%, which was significantly higher than that of traditional NPs based on U-absent copolymers (<15%). In addition, MTX-loaded mPEG-HPG-g-U NPs also demonstrated an acidity-accelerated drug release behavior. Oxford University Press 2014-11 2014-10-20 /pmc/articles/PMC4669001/ /pubmed/26816622 http://dx.doi.org/10.1093/rb/rbu010 Text en © The Author(s) 2014. Published by Oxford University Press. 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 reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Cai, Teng-Teng Lei, Qi Yang, Bin Jia, Hui-Zhen Cheng, Hong Liu, Li-Han Zeng, Xuan Feng, Jun Zhuo, Ren-Xi Zhang, Xian-Zheng Utilization of H-bond interaction of nucleobase Uralic with antitumor methotrexate to design drug carrier with ultrahigh loading efficiency and pH-responsive drug release |
title | Utilization of H-bond interaction of nucleobase Uralic with antitumor methotrexate to design drug carrier with ultrahigh loading efficiency and pH-responsive drug release |
title_full | Utilization of H-bond interaction of nucleobase Uralic with antitumor methotrexate to design drug carrier with ultrahigh loading efficiency and pH-responsive drug release |
title_fullStr | Utilization of H-bond interaction of nucleobase Uralic with antitumor methotrexate to design drug carrier with ultrahigh loading efficiency and pH-responsive drug release |
title_full_unstemmed | Utilization of H-bond interaction of nucleobase Uralic with antitumor methotrexate to design drug carrier with ultrahigh loading efficiency and pH-responsive drug release |
title_short | Utilization of H-bond interaction of nucleobase Uralic with antitumor methotrexate to design drug carrier with ultrahigh loading efficiency and pH-responsive drug release |
title_sort | utilization of h-bond interaction of nucleobase uralic with antitumor methotrexate to design drug carrier with ultrahigh loading efficiency and ph-responsive drug release |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4669001/ https://www.ncbi.nlm.nih.gov/pubmed/26816622 http://dx.doi.org/10.1093/rb/rbu010 |
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