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Delivery of Lipid Nanoparticles with ROS Probes for Improved Visualization of Hepatocellular Carcinoma

Reactive oxygen species (ROS) are highly reactive products of the cell metabolism derived from oxygen molecules, and their abundant level is observed in many diseases, particularly tumors, such as hepatocellular carcinoma (HCC). In vivo imaging of ROS is a necessary tool in preclinical research to e...

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Autores principales: Shashkovskaya, Vera S., Vetosheva, Polina I., Shokhina, Arina G., Aparin, Ilya O., Prikazchikova, Tatiana A., Mikaelyan, Arsen S., Kotelevtsev, Yuri V., Belousov, Vsevolod V., Zatsepin, Timofei S., Abakumova, Tatiana O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10376883/
https://www.ncbi.nlm.nih.gov/pubmed/37509423
http://dx.doi.org/10.3390/biomedicines11071783
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author Shashkovskaya, Vera S.
Vetosheva, Polina I.
Shokhina, Arina G.
Aparin, Ilya O.
Prikazchikova, Tatiana A.
Mikaelyan, Arsen S.
Kotelevtsev, Yuri V.
Belousov, Vsevolod V.
Zatsepin, Timofei S.
Abakumova, Tatiana O.
author_facet Shashkovskaya, Vera S.
Vetosheva, Polina I.
Shokhina, Arina G.
Aparin, Ilya O.
Prikazchikova, Tatiana A.
Mikaelyan, Arsen S.
Kotelevtsev, Yuri V.
Belousov, Vsevolod V.
Zatsepin, Timofei S.
Abakumova, Tatiana O.
author_sort Shashkovskaya, Vera S.
collection PubMed
description Reactive oxygen species (ROS) are highly reactive products of the cell metabolism derived from oxygen molecules, and their abundant level is observed in many diseases, particularly tumors, such as hepatocellular carcinoma (HCC). In vivo imaging of ROS is a necessary tool in preclinical research to evaluate the efficacy of drugs with antioxidant activity and for diagnosis and monitoring of diseases. However, most known sensors cannot be used for in vivo experiments due to low stability in the blood and rapid elimination from the body. In this work, we focused on the development of an effective delivery system of fluorescent probes for intravital ROS visualization using the HCC model. We have synthesized various lipid nanoparticles (LNPs) loaded with ROS-inducible hydrocyanine pro-fluorescent dye or plasmid DNA (pDNA) with genetically encoded protein sensors of hydrogen peroxide (HyPer7). LNP with an average diameter of 110 ± 12 nm, characterized by increased stability and pDNA loading efficiency (64 ± 7%), demonstrated preferable accumulation in the liver compared to 170 nm LNPs. We evaluated cytotoxicity and demonstrated the efficacy of hydrocyanine-5 and HyPer7 formulated in LNP for ROS visualization in mouse hepatocytes (AML12 cells) and in the mouse xenograft model of HCC. Our results demonstrate that obtained LNP could be a valuable tool in preclinical research for visualization ROS in liver diseases.
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spelling pubmed-103768832023-07-29 Delivery of Lipid Nanoparticles with ROS Probes for Improved Visualization of Hepatocellular Carcinoma Shashkovskaya, Vera S. Vetosheva, Polina I. Shokhina, Arina G. Aparin, Ilya O. Prikazchikova, Tatiana A. Mikaelyan, Arsen S. Kotelevtsev, Yuri V. Belousov, Vsevolod V. Zatsepin, Timofei S. Abakumova, Tatiana O. Biomedicines Communication Reactive oxygen species (ROS) are highly reactive products of the cell metabolism derived from oxygen molecules, and their abundant level is observed in many diseases, particularly tumors, such as hepatocellular carcinoma (HCC). In vivo imaging of ROS is a necessary tool in preclinical research to evaluate the efficacy of drugs with antioxidant activity and for diagnosis and monitoring of diseases. However, most known sensors cannot be used for in vivo experiments due to low stability in the blood and rapid elimination from the body. In this work, we focused on the development of an effective delivery system of fluorescent probes for intravital ROS visualization using the HCC model. We have synthesized various lipid nanoparticles (LNPs) loaded with ROS-inducible hydrocyanine pro-fluorescent dye or plasmid DNA (pDNA) with genetically encoded protein sensors of hydrogen peroxide (HyPer7). LNP with an average diameter of 110 ± 12 nm, characterized by increased stability and pDNA loading efficiency (64 ± 7%), demonstrated preferable accumulation in the liver compared to 170 nm LNPs. We evaluated cytotoxicity and demonstrated the efficacy of hydrocyanine-5 and HyPer7 formulated in LNP for ROS visualization in mouse hepatocytes (AML12 cells) and in the mouse xenograft model of HCC. Our results demonstrate that obtained LNP could be a valuable tool in preclinical research for visualization ROS in liver diseases. MDPI 2023-06-21 /pmc/articles/PMC10376883/ /pubmed/37509423 http://dx.doi.org/10.3390/biomedicines11071783 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Communication
Shashkovskaya, Vera S.
Vetosheva, Polina I.
Shokhina, Arina G.
Aparin, Ilya O.
Prikazchikova, Tatiana A.
Mikaelyan, Arsen S.
Kotelevtsev, Yuri V.
Belousov, Vsevolod V.
Zatsepin, Timofei S.
Abakumova, Tatiana O.
Delivery of Lipid Nanoparticles with ROS Probes for Improved Visualization of Hepatocellular Carcinoma
title Delivery of Lipid Nanoparticles with ROS Probes for Improved Visualization of Hepatocellular Carcinoma
title_full Delivery of Lipid Nanoparticles with ROS Probes for Improved Visualization of Hepatocellular Carcinoma
title_fullStr Delivery of Lipid Nanoparticles with ROS Probes for Improved Visualization of Hepatocellular Carcinoma
title_full_unstemmed Delivery of Lipid Nanoparticles with ROS Probes for Improved Visualization of Hepatocellular Carcinoma
title_short Delivery of Lipid Nanoparticles with ROS Probes for Improved Visualization of Hepatocellular Carcinoma
title_sort delivery of lipid nanoparticles with ros probes for improved visualization of hepatocellular carcinoma
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10376883/
https://www.ncbi.nlm.nih.gov/pubmed/37509423
http://dx.doi.org/10.3390/biomedicines11071783
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