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Radiation‐Sensitive Dendrimer‐Based Drug Delivery System

Combination of chemotherapy and radiotherapy is used to enhance local drug delivery while reducing off‐target tissue effects. Anticancer drug doxorubicin (DOX) is loaded into l‐cysteine modified G4.5 dendrimer (GC/DOX) and released at different pH values in the presence and absence of γ‐radiation. P...

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Autores principales: Wu, Szu‐Yuan, Chou, Hsiao‐Ying, Yuh, Chiou‐Hwa, Mekuria, Shewaye Lakew, Kao, Yu‐Chih, Tsai, Hsieh‐Chih
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5827102/
https://www.ncbi.nlm.nih.gov/pubmed/29610720
http://dx.doi.org/10.1002/advs.201700339
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author Wu, Szu‐Yuan
Chou, Hsiao‐Ying
Yuh, Chiou‐Hwa
Mekuria, Shewaye Lakew
Kao, Yu‐Chih
Tsai, Hsieh‐Chih
author_facet Wu, Szu‐Yuan
Chou, Hsiao‐Ying
Yuh, Chiou‐Hwa
Mekuria, Shewaye Lakew
Kao, Yu‐Chih
Tsai, Hsieh‐Chih
author_sort Wu, Szu‐Yuan
collection PubMed
description Combination of chemotherapy and radiotherapy is used to enhance local drug delivery while reducing off‐target tissue effects. Anticancer drug doxorubicin (DOX) is loaded into l‐cysteine modified G4.5 dendrimer (GC/DOX) and released at different pH values in the presence and absence of γ‐radiation. Presence of γ‐radiation significantly improves DOX release from the GC/DOX under acidic pH conditions, suggesting that GC dendrimer is a radiation‐sensitive drug delivery system. GC/DOX is further evaluated by determining cytotoxicity in uterine cervical carcinoma HeLa cells. GC/DOX shows high affinity for cancer cells and effective drug release following an external stimulus (radiation exposure), whereas an in vivo zebrafish study confirms that l‐cysteine acts as a radiosensitizer. GC/DOX treatment combined with radiotherapy synergistically and successfully inhibits cancer cell growth.
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spelling pubmed-58271022018-04-02 Radiation‐Sensitive Dendrimer‐Based Drug Delivery System Wu, Szu‐Yuan Chou, Hsiao‐Ying Yuh, Chiou‐Hwa Mekuria, Shewaye Lakew Kao, Yu‐Chih Tsai, Hsieh‐Chih Adv Sci (Weinh) Full Papers Combination of chemotherapy and radiotherapy is used to enhance local drug delivery while reducing off‐target tissue effects. Anticancer drug doxorubicin (DOX) is loaded into l‐cysteine modified G4.5 dendrimer (GC/DOX) and released at different pH values in the presence and absence of γ‐radiation. Presence of γ‐radiation significantly improves DOX release from the GC/DOX under acidic pH conditions, suggesting that GC dendrimer is a radiation‐sensitive drug delivery system. GC/DOX is further evaluated by determining cytotoxicity in uterine cervical carcinoma HeLa cells. GC/DOX shows high affinity for cancer cells and effective drug release following an external stimulus (radiation exposure), whereas an in vivo zebrafish study confirms that l‐cysteine acts as a radiosensitizer. GC/DOX treatment combined with radiotherapy synergistically and successfully inhibits cancer cell growth. John Wiley and Sons Inc. 2017-12-05 /pmc/articles/PMC5827102/ /pubmed/29610720 http://dx.doi.org/10.1002/advs.201700339 Text en © 2017 The Authors. Published by WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Full Papers
Wu, Szu‐Yuan
Chou, Hsiao‐Ying
Yuh, Chiou‐Hwa
Mekuria, Shewaye Lakew
Kao, Yu‐Chih
Tsai, Hsieh‐Chih
Radiation‐Sensitive Dendrimer‐Based Drug Delivery System
title Radiation‐Sensitive Dendrimer‐Based Drug Delivery System
title_full Radiation‐Sensitive Dendrimer‐Based Drug Delivery System
title_fullStr Radiation‐Sensitive Dendrimer‐Based Drug Delivery System
title_full_unstemmed Radiation‐Sensitive Dendrimer‐Based Drug Delivery System
title_short Radiation‐Sensitive Dendrimer‐Based Drug Delivery System
title_sort radiation‐sensitive dendrimer‐based drug delivery system
topic Full Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5827102/
https://www.ncbi.nlm.nih.gov/pubmed/29610720
http://dx.doi.org/10.1002/advs.201700339
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