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pH/redox sensitive nanoparticles with platinum(iv) prodrugs and doxorubicin enhance chemotherapy in ovarian cancer

pH/redox sensitive, dual drug loaded nanoparticles were prepared from poly(ethylene glycol)-block-poly(l-lysine) (PEG-b-PLL) for improving cancer therapy. Platinum(iv) and cis-aconitic anhydride-doxorubicin (CAD) were anchored to lysine residual amine groups of PLL to form polymer prodrug conjugates...

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Autores principales: Zhang, Guyu, Zhu, Yimin, Wang, Yushu, Wei, Dengshuai, Wu, Yixin, Zheng, Liuchun, Bai, Huimin, Xiao, Haihua, Zhang, Zhenyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9065746/
https://www.ncbi.nlm.nih.gov/pubmed/35515556
http://dx.doi.org/10.1039/c9ra04034j
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author Zhang, Guyu
Zhu, Yimin
Wang, Yushu
Wei, Dengshuai
Wu, Yixin
Zheng, Liuchun
Bai, Huimin
Xiao, Haihua
Zhang, Zhenyu
author_facet Zhang, Guyu
Zhu, Yimin
Wang, Yushu
Wei, Dengshuai
Wu, Yixin
Zheng, Liuchun
Bai, Huimin
Xiao, Haihua
Zhang, Zhenyu
author_sort Zhang, Guyu
collection PubMed
description pH/redox sensitive, dual drug loaded nanoparticles were prepared from poly(ethylene glycol)-block-poly(l-lysine) (PEG-b-PLL) for improving cancer therapy. Platinum(iv) and cis-aconitic anhydride-doxorubicin (CAD) were anchored to lysine residual amine groups of PLL to form polymer prodrug conjugates, which then self-assembled into nanoparticles with hydrophobic platinum(iv) prodrugs and CAD as the core. The nanoparticles were stable in neutral environments, but once under acidic and reductive conditions, the drugs were rapidly released. The dual-loaded nanoparticles had comparable intracellular toxicity to the regimen of combined application of free cisplatin and doxorubicin.
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spelling pubmed-90657462022-05-04 pH/redox sensitive nanoparticles with platinum(iv) prodrugs and doxorubicin enhance chemotherapy in ovarian cancer Zhang, Guyu Zhu, Yimin Wang, Yushu Wei, Dengshuai Wu, Yixin Zheng, Liuchun Bai, Huimin Xiao, Haihua Zhang, Zhenyu RSC Adv Chemistry pH/redox sensitive, dual drug loaded nanoparticles were prepared from poly(ethylene glycol)-block-poly(l-lysine) (PEG-b-PLL) for improving cancer therapy. Platinum(iv) and cis-aconitic anhydride-doxorubicin (CAD) were anchored to lysine residual amine groups of PLL to form polymer prodrug conjugates, which then self-assembled into nanoparticles with hydrophobic platinum(iv) prodrugs and CAD as the core. The nanoparticles were stable in neutral environments, but once under acidic and reductive conditions, the drugs were rapidly released. The dual-loaded nanoparticles had comparable intracellular toxicity to the regimen of combined application of free cisplatin and doxorubicin. The Royal Society of Chemistry 2019-07-02 /pmc/articles/PMC9065746/ /pubmed/35515556 http://dx.doi.org/10.1039/c9ra04034j Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Zhang, Guyu
Zhu, Yimin
Wang, Yushu
Wei, Dengshuai
Wu, Yixin
Zheng, Liuchun
Bai, Huimin
Xiao, Haihua
Zhang, Zhenyu
pH/redox sensitive nanoparticles with platinum(iv) prodrugs and doxorubicin enhance chemotherapy in ovarian cancer
title pH/redox sensitive nanoparticles with platinum(iv) prodrugs and doxorubicin enhance chemotherapy in ovarian cancer
title_full pH/redox sensitive nanoparticles with platinum(iv) prodrugs and doxorubicin enhance chemotherapy in ovarian cancer
title_fullStr pH/redox sensitive nanoparticles with platinum(iv) prodrugs and doxorubicin enhance chemotherapy in ovarian cancer
title_full_unstemmed pH/redox sensitive nanoparticles with platinum(iv) prodrugs and doxorubicin enhance chemotherapy in ovarian cancer
title_short pH/redox sensitive nanoparticles with platinum(iv) prodrugs and doxorubicin enhance chemotherapy in ovarian cancer
title_sort ph/redox sensitive nanoparticles with platinum(iv) prodrugs and doxorubicin enhance chemotherapy in ovarian cancer
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9065746/
https://www.ncbi.nlm.nih.gov/pubmed/35515556
http://dx.doi.org/10.1039/c9ra04034j
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