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Novel pH-sensitive zinc phthalocyanine assembled with albumin for tumor targeting and treatment

PURPOSE: Zinc phthalocyanine (ZnPc) has been applied widely in photodynamic therapy (PDT) with high ROS-production capacity and intense absorption in the near-infrared region. However, weak tumor targeting and the aggregation tendency of ZnPc seriously affect the therapeutic effect of PDT. Therefore...

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Autores principales: Wang, Ying, Zheng, Ke, Xuan, Guangshan, Huang, Mingdong, Xue, Jinping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6251464/
https://www.ncbi.nlm.nih.gov/pubmed/30538452
http://dx.doi.org/10.2147/IJN.S181199
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author Wang, Ying
Zheng, Ke
Xuan, Guangshan
Huang, Mingdong
Xue, Jinping
author_facet Wang, Ying
Zheng, Ke
Xuan, Guangshan
Huang, Mingdong
Xue, Jinping
author_sort Wang, Ying
collection PubMed
description PURPOSE: Zinc phthalocyanine (ZnPc) has been applied widely in photodynamic therapy (PDT) with high ROS-production capacity and intense absorption in the near-infrared region. However, weak tumor targeting and the aggregation tendency of ZnPc seriously affect the therapeutic effect of PDT. Therefore, overcoming the aggregation of ZnPc and enhancing its antitumor effect were the purpose of this study. METHODS: In this study, we first found that the aggregation behaviors of the photosensitizer ZnPc(TAP)(4), ZnPc substituted by tertiary amine groups, were regulated finely by pH and that ZnPc(TAP)(4) could be disaggregated gradually as the pH descended. ZnPc(TAP)(4) and human serum albumin (HSA) molecules were assembled into nanoparticles (NPs) for tumor targeting. Meanwhile, the chemotherapy drug paclitaxel (Ptx) was loaded into HSA NPs together with ZnPc(TAP)(4) for dual antitumor effects. HSA NPs loading both ZnPc(TAP)(4) and Ptx (NP–ZnPc[TAP](4)–Ptx) were characterized by particle size and in vitro release. Cytotoxicity, subcellular localization, tumor targeting, and anticancer effect in vivo were investigated respectively. RESULTS: We found that NP–ZnPc(TAP)(4)–Ptx had good stability with qualifying particle size. Interestingly, ZnPc(TAP)(4) was released from the NPs and the photodynamic activity enhanced in the acidic environment of tumor. In addition, NP–ZnPc(TAP)(4)–Ptx had prominent cytotoxicity and time-dependent subcellular localization characteristics. Through a three-dimensional animal imaging system, NP–ZnPc(TAP)(4)–Ptx showed much-enhanced tumor targeting in tumor-bearing mice. Above all, NP–ZnPc(TAP)(4)–Ptx was demonstrated to have the synergistic anticancer effect of PDT and chemotherapy. CONCLUSION: NP–ZnPc(TAP)(4)–Ptx had enhanced tumor targeting for the pH-sensitive property of ZnPc(TAP)(4) and the transport function of HSA. NP–ZnPc(TAP)(4)–Ptx possessed a double-anticancer effect through the combination of ZnPc(TAP)(4) and Ptx. This drug-delivery system may also be used to carry chemotherapy drugs other than Ptx for improving antitumor effects.
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spelling pubmed-62514642018-12-11 Novel pH-sensitive zinc phthalocyanine assembled with albumin for tumor targeting and treatment Wang, Ying Zheng, Ke Xuan, Guangshan Huang, Mingdong Xue, Jinping Int J Nanomedicine Original Research PURPOSE: Zinc phthalocyanine (ZnPc) has been applied widely in photodynamic therapy (PDT) with high ROS-production capacity and intense absorption in the near-infrared region. However, weak tumor targeting and the aggregation tendency of ZnPc seriously affect the therapeutic effect of PDT. Therefore, overcoming the aggregation of ZnPc and enhancing its antitumor effect were the purpose of this study. METHODS: In this study, we first found that the aggregation behaviors of the photosensitizer ZnPc(TAP)(4), ZnPc substituted by tertiary amine groups, were regulated finely by pH and that ZnPc(TAP)(4) could be disaggregated gradually as the pH descended. ZnPc(TAP)(4) and human serum albumin (HSA) molecules were assembled into nanoparticles (NPs) for tumor targeting. Meanwhile, the chemotherapy drug paclitaxel (Ptx) was loaded into HSA NPs together with ZnPc(TAP)(4) for dual antitumor effects. HSA NPs loading both ZnPc(TAP)(4) and Ptx (NP–ZnPc[TAP](4)–Ptx) were characterized by particle size and in vitro release. Cytotoxicity, subcellular localization, tumor targeting, and anticancer effect in vivo were investigated respectively. RESULTS: We found that NP–ZnPc(TAP)(4)–Ptx had good stability with qualifying particle size. Interestingly, ZnPc(TAP)(4) was released from the NPs and the photodynamic activity enhanced in the acidic environment of tumor. In addition, NP–ZnPc(TAP)(4)–Ptx had prominent cytotoxicity and time-dependent subcellular localization characteristics. Through a three-dimensional animal imaging system, NP–ZnPc(TAP)(4)–Ptx showed much-enhanced tumor targeting in tumor-bearing mice. Above all, NP–ZnPc(TAP)(4)–Ptx was demonstrated to have the synergistic anticancer effect of PDT and chemotherapy. CONCLUSION: NP–ZnPc(TAP)(4)–Ptx had enhanced tumor targeting for the pH-sensitive property of ZnPc(TAP)(4) and the transport function of HSA. NP–ZnPc(TAP)(4)–Ptx possessed a double-anticancer effect through the combination of ZnPc(TAP)(4) and Ptx. This drug-delivery system may also be used to carry chemotherapy drugs other than Ptx for improving antitumor effects. Dove Medical Press 2018-11-19 /pmc/articles/PMC6251464/ /pubmed/30538452 http://dx.doi.org/10.2147/IJN.S181199 Text en © 2018 Wang et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Wang, Ying
Zheng, Ke
Xuan, Guangshan
Huang, Mingdong
Xue, Jinping
Novel pH-sensitive zinc phthalocyanine assembled with albumin for tumor targeting and treatment
title Novel pH-sensitive zinc phthalocyanine assembled with albumin for tumor targeting and treatment
title_full Novel pH-sensitive zinc phthalocyanine assembled with albumin for tumor targeting and treatment
title_fullStr Novel pH-sensitive zinc phthalocyanine assembled with albumin for tumor targeting and treatment
title_full_unstemmed Novel pH-sensitive zinc phthalocyanine assembled with albumin for tumor targeting and treatment
title_short Novel pH-sensitive zinc phthalocyanine assembled with albumin for tumor targeting and treatment
title_sort novel ph-sensitive zinc phthalocyanine assembled with albumin for tumor targeting and treatment
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6251464/
https://www.ncbi.nlm.nih.gov/pubmed/30538452
http://dx.doi.org/10.2147/IJN.S181199
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