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

Author:

Shashkovskaya Vera S.12,Vetosheva Polina I.3,Shokhina Arina G.245,Aparin Ilya O.35,Prikazchikova Tatiana A.6,Mikaelyan Arsen S.7ORCID,Kotelevtsev Yuri V.1ORCID,Belousov Vsevolod V.245,Zatsepin Timofei S.6ORCID,Abakumova Tatiana O.2ORCID

Affiliation:

1. Vladimir Zelman Center for Neurobiology and Brain Rehabilitation, Skolkovo Institute of Science and Technology, 121205 Moscow, Russia

2. Institute of Translational Medicine, Pirogov Russian National Research Medical University, 117997 Moscow, Russia

3. Center for Molecular and Cellular Biology, Skolkovo Institute of Science and Technology, 121205 Moscow, Russia

4. Federal Center of Brain Research and Neurotechnologies, Federal Medical Biological Agency, 119435 Moscow, Russia

5. Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry, 117997 Moscow, Russia

6. Department of Chemistry, M. V. Lomonosov Moscow State University, 119991 Moscow, Russia

7. Koltsov Institute of Developmental Biology of Russian Academy of Sciences, 152742 Moscow, Russia

Abstract

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.

Funder

RSF

President MK

Publisher

MDPI AG

Subject

General Biochemistry, Genetics and Molecular Biology,Medicine (miscellaneous)

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