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Low Dose of Ti3C2 MXene Quantum Dots Mitigate SARS‐CoV‐2 Infection.

Authors :
Yilmazer, Açelya
Alagarsamy, Keshav Narayan
Gokce, Cemile
Summak, Gokce Yagmur
Rafieerad, Alireza
Bayrakdar, Fatma
Ozturk, Berfin Ilayda
Aktuna, Suleyman
Delogu, Lucia Gemma
Unal, Mehmet Altay
Dhingra, Sanjiv
Source :
Small Methods; Aug2023, Vol. 7 Issue 8, p1-13, 13p
Publication Year :
2023

Abstract

MXene QDs (MQDs) have been effectively used in several fields of biomedical research. Considering the role of hyperactivation of immune system in infectious diseases, especially in COVID‐19, MQDs stand as a potential candidate as a nanotherapeutic against viral infections. However, the efficacy of MQDs against SARS‐CoV‐2 infection has not been tested yet. In this study, Ti3C2 MQDs are synthesized and their potential in mitigating SARS‐CoV‐2 infection is investigated. Physicochemical characterization suggests that MQDs are enriched with abundance of bioactive functional groups such as oxygen, hydrogen, fluorine, and chlorine groups as well as surface titanium oxides. The efficacy of MQDs is tested in VeroE6 cells infected with SARS‐CoV‐2. These data demonstrate that the treatment with MQDs is able to mitigate multiplication of virus particles, only at very low doses such as 0,15 µg mL−1. Furthermore, to understand the mechanisms of MQD‐mediated anti‐COVID properties, global proteomics analysis are performed and determined differentially expressed proteins between MQD‐treated and untreated cells. Data reveal that MQDs interfere with the viral life cycle through different mechanisms including the Ca2+ signaling pathway, IFN‐α response, virus internalization, replication, and translation. These findings suggest that MQDs can be employed to develop future immunoengineering‐based nanotherapeutics strategies against SARS‐CoV‐2 and other viral infections. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
23669608
Volume :
7
Issue :
8
Database :
Complementary Index
Journal :
Small Methods
Publication Type :
Academic Journal
Accession number :
169873825
Full Text :
https://doi.org/10.1002/smtd.202300044