A smart O2-generating nanocarrier optimizes drug transportation comprehensively for chemotherapy improving

Drug transportation is impeded by various barriers in the hypoxic solid tumor, resulting in compromised anticancer efficacy. Herein, a solid lipid monostearin (MS)-coated CaO2/MnO2 nanocarrier was designed to optimize doxorubicin (DOX) transportation comprehensively for chemotherapy enhancement. The...

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Autores principales: Xiaojuan Zhang, Chuanchuan He, Yun Sun, Xiaoguang Liu, Yan Chen, Chen Chen, Ruicong Yan, Ting Fan, Tan Yang, Yao Lu, Jun Luo, Xiang Ma, Guangya Xiang
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Lenguaje:EN
Publicado: Elsevier 2021
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Acceso en línea:https://doaj.org/article/6ba987ace84c45338883a028a6da140e
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spelling oai:doaj.org-article:6ba987ace84c45338883a028a6da140e2021-12-02T05:01:23ZA smart O2-generating nanocarrier optimizes drug transportation comprehensively for chemotherapy improving2211-383510.1016/j.apsb.2021.04.021https://doaj.org/article/6ba987ace84c45338883a028a6da140e2021-11-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S2211383521001611https://doaj.org/toc/2211-3835Drug transportation is impeded by various barriers in the hypoxic solid tumor, resulting in compromised anticancer efficacy. Herein, a solid lipid monostearin (MS)-coated CaO2/MnO2 nanocarrier was designed to optimize doxorubicin (DOX) transportation comprehensively for chemotherapy enhancement. The MS shell of nanoparticles could be destroyed selectively by highly-expressed lipase within cancer cells, exposing water-sensitive cores to release DOX and produce O2. After the cancer cell death, the core-exposed nanoparticles could be further liberated and continue to react with water in the tumor extracellular matrix (ECM) and thoroughly release O2 and DOX, which exhibited cytotoxicity to neighboring cells. Small DOX molecules could readily diffuse through ECM, in which the collagen deposition was decreased by O2-mediated hypoxia-inducible factor-1 inhibition, leading to synergistically improved drug penetration. Concurrently, DOX-efflux-associated P-glycoprotein was also inhibited by O2, prolonging drug retention in cancer cells. Overall, the DOX transporting processes from nanoparticles to deep tumor cells including drug release, penetration, and retention were optimized comprehensively, which significantly boosted antitumor benefits.Xiaojuan ZhangChuanchuan HeYun SunXiaoguang LiuYan ChenChen ChenRuicong YanTing FanTan YangYao LuJun LuoXiang MaGuangya XiangElsevierarticleTumorNanoparticleChemotherapyHypoxiaHIF-1TransportationTherapeutics. PharmacologyRM1-950ENActa Pharmaceutica Sinica B, Vol 11, Iss 11, Pp 3608-3621 (2021)
institution DOAJ
collection DOAJ
language EN
topic Tumor
Nanoparticle
Chemotherapy
Hypoxia
HIF-1
Transportation
Therapeutics. Pharmacology
RM1-950
spellingShingle Tumor
Nanoparticle
Chemotherapy
Hypoxia
HIF-1
Transportation
Therapeutics. Pharmacology
RM1-950
Xiaojuan Zhang
Chuanchuan He
Yun Sun
Xiaoguang Liu
Yan Chen
Chen Chen
Ruicong Yan
Ting Fan
Tan Yang
Yao Lu
Jun Luo
Xiang Ma
Guangya Xiang
A smart O2-generating nanocarrier optimizes drug transportation comprehensively for chemotherapy improving
description Drug transportation is impeded by various barriers in the hypoxic solid tumor, resulting in compromised anticancer efficacy. Herein, a solid lipid monostearin (MS)-coated CaO2/MnO2 nanocarrier was designed to optimize doxorubicin (DOX) transportation comprehensively for chemotherapy enhancement. The MS shell of nanoparticles could be destroyed selectively by highly-expressed lipase within cancer cells, exposing water-sensitive cores to release DOX and produce O2. After the cancer cell death, the core-exposed nanoparticles could be further liberated and continue to react with water in the tumor extracellular matrix (ECM) and thoroughly release O2 and DOX, which exhibited cytotoxicity to neighboring cells. Small DOX molecules could readily diffuse through ECM, in which the collagen deposition was decreased by O2-mediated hypoxia-inducible factor-1 inhibition, leading to synergistically improved drug penetration. Concurrently, DOX-efflux-associated P-glycoprotein was also inhibited by O2, prolonging drug retention in cancer cells. Overall, the DOX transporting processes from nanoparticles to deep tumor cells including drug release, penetration, and retention were optimized comprehensively, which significantly boosted antitumor benefits.
format article
author Xiaojuan Zhang
Chuanchuan He
Yun Sun
Xiaoguang Liu
Yan Chen
Chen Chen
Ruicong Yan
Ting Fan
Tan Yang
Yao Lu
Jun Luo
Xiang Ma
Guangya Xiang
author_facet Xiaojuan Zhang
Chuanchuan He
Yun Sun
Xiaoguang Liu
Yan Chen
Chen Chen
Ruicong Yan
Ting Fan
Tan Yang
Yao Lu
Jun Luo
Xiang Ma
Guangya Xiang
author_sort Xiaojuan Zhang
title A smart O2-generating nanocarrier optimizes drug transportation comprehensively for chemotherapy improving
title_short A smart O2-generating nanocarrier optimizes drug transportation comprehensively for chemotherapy improving
title_full A smart O2-generating nanocarrier optimizes drug transportation comprehensively for chemotherapy improving
title_fullStr A smart O2-generating nanocarrier optimizes drug transportation comprehensively for chemotherapy improving
title_full_unstemmed A smart O2-generating nanocarrier optimizes drug transportation comprehensively for chemotherapy improving
title_sort smart o2-generating nanocarrier optimizes drug transportation comprehensively for chemotherapy improving
publisher Elsevier
publishDate 2021
url https://doaj.org/article/6ba987ace84c45338883a028a6da140e
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