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NIR responsive liposomal system for rapid release of drugs in cancer therapy

To design a rapid release liposomal system for cancer therapy, a NIR responsive bubble-generating thermosensitive liposome (BTSL) system combined with photothermal agent (Cypate), doxorubicin (DOX), and NH(4)HCO(3) was developed. Cypate/DOX-BTSL exhibited a good aqueous stability, photostability, an...

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Autores principales: Chen, Ming-Mao, Liu, Yuan-Yuan, Su, Guang-Hao, Song, Fei-Fei, Liu, Yan, Zhang, Qi-Qing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5473596/
https://www.ncbi.nlm.nih.gov/pubmed/28652729
http://dx.doi.org/10.2147/IJN.S130861
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author Chen, Ming-Mao
Liu, Yuan-Yuan
Su, Guang-Hao
Song, Fei-Fei
Liu, Yan
Zhang, Qi-Qing
author_facet Chen, Ming-Mao
Liu, Yuan-Yuan
Su, Guang-Hao
Song, Fei-Fei
Liu, Yan
Zhang, Qi-Qing
author_sort Chen, Ming-Mao
collection PubMed
description To design a rapid release liposomal system for cancer therapy, a NIR responsive bubble-generating thermosensitive liposome (BTSL) system combined with photothermal agent (Cypate), doxorubicin (DOX), and NH(4)HCO(3) was developed. Cypate/DOX-BTSL exhibited a good aqueous stability, photostability, and photothermal effect. In vitro release suggested that the amounts of DOX released from BTSL were obviously higher than that of (NH(4))(2)SO(4) liposomes at 42°C. After NIR irradiation, the hyperthermic temperature induced by Cypate led to the decomposition of NH(4)HCO(3) and the generation of a large number of CO(2) bubbles, triggering a rapid release of drugs. Confocal laser scanning microscope and acridine orange staining indicated that Cypate/DOX-BTSL upon irradiation could facilitate to disrupt the lysosomal membranes and realize endolysosomal escape into cytosol, improving the intracellular uptake of DOX clearly. MTT and trypan blue staining implied that the cell damage of Cypate/DOX-BTSL with NIR irradiation was more severe than that in the groups without irradiation. In vivo results indicated that Cypate/DOX-BTSL with irradiation could dramatically increase the accumulation of DOX in tumor, inhibit tumor growth, and reduce systemic side effects of DOX. These data demonstrated that Cypate/DOX-BTSL has the potential to be used as a NIR responsive liposomal system for a rapid release of drugs in thermochemotherapy.
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spelling pubmed-54735962017-06-26 NIR responsive liposomal system for rapid release of drugs in cancer therapy Chen, Ming-Mao Liu, Yuan-Yuan Su, Guang-Hao Song, Fei-Fei Liu, Yan Zhang, Qi-Qing Int J Nanomedicine Original Research To design a rapid release liposomal system for cancer therapy, a NIR responsive bubble-generating thermosensitive liposome (BTSL) system combined with photothermal agent (Cypate), doxorubicin (DOX), and NH(4)HCO(3) was developed. Cypate/DOX-BTSL exhibited a good aqueous stability, photostability, and photothermal effect. In vitro release suggested that the amounts of DOX released from BTSL were obviously higher than that of (NH(4))(2)SO(4) liposomes at 42°C. After NIR irradiation, the hyperthermic temperature induced by Cypate led to the decomposition of NH(4)HCO(3) and the generation of a large number of CO(2) bubbles, triggering a rapid release of drugs. Confocal laser scanning microscope and acridine orange staining indicated that Cypate/DOX-BTSL upon irradiation could facilitate to disrupt the lysosomal membranes and realize endolysosomal escape into cytosol, improving the intracellular uptake of DOX clearly. MTT and trypan blue staining implied that the cell damage of Cypate/DOX-BTSL with NIR irradiation was more severe than that in the groups without irradiation. In vivo results indicated that Cypate/DOX-BTSL with irradiation could dramatically increase the accumulation of DOX in tumor, inhibit tumor growth, and reduce systemic side effects of DOX. These data demonstrated that Cypate/DOX-BTSL has the potential to be used as a NIR responsive liposomal system for a rapid release of drugs in thermochemotherapy. Dove Medical Press 2017-06-06 /pmc/articles/PMC5473596/ /pubmed/28652729 http://dx.doi.org/10.2147/IJN.S130861 Text en © 2017 Chen 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
Chen, Ming-Mao
Liu, Yuan-Yuan
Su, Guang-Hao
Song, Fei-Fei
Liu, Yan
Zhang, Qi-Qing
NIR responsive liposomal system for rapid release of drugs in cancer therapy
title NIR responsive liposomal system for rapid release of drugs in cancer therapy
title_full NIR responsive liposomal system for rapid release of drugs in cancer therapy
title_fullStr NIR responsive liposomal system for rapid release of drugs in cancer therapy
title_full_unstemmed NIR responsive liposomal system for rapid release of drugs in cancer therapy
title_short NIR responsive liposomal system for rapid release of drugs in cancer therapy
title_sort nir responsive liposomal system for rapid release of drugs in cancer therapy
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5473596/
https://www.ncbi.nlm.nih.gov/pubmed/28652729
http://dx.doi.org/10.2147/IJN.S130861
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