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Liposomal nanotheranostics for multimode targeted in vivo bioimaging and near‐infrared light mediated cancer therapy

Developing a nanotheranostic agent with better image resolution and high accumulation into solid tumor microenvironment is a challenging task. Herein, we established a light mediated phototriggered strategy for enhanced tumor accumulation of nanohybrids. A multifunctional liposome based nanotheranos...

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Autores principales: Prasad, Rajendra, Jain, Nishant K., Yadav, Amit S., Chauhan, Deepak S., Devrukhkar, Janhavi, Kumawat, Mukesh K., Shinde, Shweta, Gorain, Mahadeo, Thakor, Avnesh S., Kundu, Gopal C., Conde, João, Srivastava, Rohit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7275035/
https://www.ncbi.nlm.nih.gov/pubmed/32504032
http://dx.doi.org/10.1038/s42003-020-1016-z
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author Prasad, Rajendra
Jain, Nishant K.
Yadav, Amit S.
Chauhan, Deepak S.
Devrukhkar, Janhavi
Kumawat, Mukesh K.
Shinde, Shweta
Gorain, Mahadeo
Thakor, Avnesh S.
Kundu, Gopal C.
Conde, João
Srivastava, Rohit
author_facet Prasad, Rajendra
Jain, Nishant K.
Yadav, Amit S.
Chauhan, Deepak S.
Devrukhkar, Janhavi
Kumawat, Mukesh K.
Shinde, Shweta
Gorain, Mahadeo
Thakor, Avnesh S.
Kundu, Gopal C.
Conde, João
Srivastava, Rohit
author_sort Prasad, Rajendra
collection PubMed
description Developing a nanotheranostic agent with better image resolution and high accumulation into solid tumor microenvironment is a challenging task. Herein, we established a light mediated phototriggered strategy for enhanced tumor accumulation of nanohybrids. A multifunctional liposome based nanotheranostics loaded with gold nanoparticles (AuNPs) and emissive graphene quantum dots (GQDs) were engineered named as NFGL. Further, doxorubicin hydrochloride was encapsulated in NFGL to exhibit phototriggered chemotherapy and functionalized with folic acid targeting ligands. Encapsulated agents showed imaging bimodality for in vivo tumor diagnosis due to their high contrast and emissive nature. Targeted NFGL nanohybrids demonstrated near infrared light (NIR, 750 nm) mediated tumor reduction because of generated heat and Reactive Oxygen Species (ROS). Moreover, NFGL nanohybrids exhibited remarkable ROS scavenging ability as compared to GQDs loaded liposomes validated by antitumor study. Hence, this approach and engineered system could open new direction for targeted imaging and cancer therapy.
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spelling pubmed-72750352020-06-16 Liposomal nanotheranostics for multimode targeted in vivo bioimaging and near‐infrared light mediated cancer therapy Prasad, Rajendra Jain, Nishant K. Yadav, Amit S. Chauhan, Deepak S. Devrukhkar, Janhavi Kumawat, Mukesh K. Shinde, Shweta Gorain, Mahadeo Thakor, Avnesh S. Kundu, Gopal C. Conde, João Srivastava, Rohit Commun Biol Article Developing a nanotheranostic agent with better image resolution and high accumulation into solid tumor microenvironment is a challenging task. Herein, we established a light mediated phototriggered strategy for enhanced tumor accumulation of nanohybrids. A multifunctional liposome based nanotheranostics loaded with gold nanoparticles (AuNPs) and emissive graphene quantum dots (GQDs) were engineered named as NFGL. Further, doxorubicin hydrochloride was encapsulated in NFGL to exhibit phototriggered chemotherapy and functionalized with folic acid targeting ligands. Encapsulated agents showed imaging bimodality for in vivo tumor diagnosis due to their high contrast and emissive nature. Targeted NFGL nanohybrids demonstrated near infrared light (NIR, 750 nm) mediated tumor reduction because of generated heat and Reactive Oxygen Species (ROS). Moreover, NFGL nanohybrids exhibited remarkable ROS scavenging ability as compared to GQDs loaded liposomes validated by antitumor study. Hence, this approach and engineered system could open new direction for targeted imaging and cancer therapy. Nature Publishing Group UK 2020-06-05 /pmc/articles/PMC7275035/ /pubmed/32504032 http://dx.doi.org/10.1038/s42003-020-1016-z Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Prasad, Rajendra
Jain, Nishant K.
Yadav, Amit S.
Chauhan, Deepak S.
Devrukhkar, Janhavi
Kumawat, Mukesh K.
Shinde, Shweta
Gorain, Mahadeo
Thakor, Avnesh S.
Kundu, Gopal C.
Conde, João
Srivastava, Rohit
Liposomal nanotheranostics for multimode targeted in vivo bioimaging and near‐infrared light mediated cancer therapy
title Liposomal nanotheranostics for multimode targeted in vivo bioimaging and near‐infrared light mediated cancer therapy
title_full Liposomal nanotheranostics for multimode targeted in vivo bioimaging and near‐infrared light mediated cancer therapy
title_fullStr Liposomal nanotheranostics for multimode targeted in vivo bioimaging and near‐infrared light mediated cancer therapy
title_full_unstemmed Liposomal nanotheranostics for multimode targeted in vivo bioimaging and near‐infrared light mediated cancer therapy
title_short Liposomal nanotheranostics for multimode targeted in vivo bioimaging and near‐infrared light mediated cancer therapy
title_sort liposomal nanotheranostics for multimode targeted in vivo bioimaging and near‐infrared light mediated cancer therapy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7275035/
https://www.ncbi.nlm.nih.gov/pubmed/32504032
http://dx.doi.org/10.1038/s42003-020-1016-z
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