Issue 43, 2024

Translocation of Ti2CO2 MXene monolayer through the cell membranes

Abstract

Nanoparticle-based therapies represent a cutting-edge direction in medical research. Ti2CO2 MXene is a novel two-dimensional transition metal carbide with a high surface area and reactivity, making it suitable for biomedical applications due to its biocompatibility. In biomedicine, Ti2CO2 MXene is particularly used in photothermal therapy, where its ability to absorb light and convert it into heat can be utilized to target and destroy cancer cells. The study of how temperature influences the interaction between nanoparticles and cell membranes is a critical aspect of this field. Our study conducts a thorough coarse-grained molecular dynamics analysis of a Ti2CO2 MXene nanosheet interacting with a phosphatidylcholine (POPC) membrane under various thermal conditions and nanosheet orientations. We show that the hydrophilic nature of the nanosheet presents a substantial barrier to membrane penetration and an increase in temperature significantly enhances the permeability of the membrane, thereby facilitating the migration of the MXene nanoparticles across it. The peak force required to translocate the nanosheet through the membrane decreases e.g., from 2150 pN at 300 kelvin to 1450 pN at 370 kelvin indicating significant reduction in resistance at higher temperatures. The study also highlights the critical role of the nanosheets' spatial orientation in cellular uptake. Our research underscores the importance of the application of MXenes for nanomedical and photothermal therapy purposes.

Graphical abstract: Translocation of Ti2CO2 MXene monolayer through the cell membranes

Supplementary files

Article information

Article type
Paper
Submitted
11 Aug 2024
Accepted
14 Sep 2024
First published
04 Oct 2024
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2024,14, 31577-31586

Translocation of Ti2CO2 MXene monolayer through the cell membranes

H. Ahmadi, R. Abdolvahab and M. Esmaeilzadeh, RSC Adv., 2024, 14, 31577 DOI: 10.1039/D4RA05821F

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