Heterojunction 2D/1D Ti3C2Tx MXene/TiO2 interfaces for efficient blood oxygenation through photocatalytic action
摘要
The process of blood oxygenation through photocatalytic action is an emerging concept in the realm of artificial lung technology, differing from current technologies that rely on the oxygenation of blood via permeable hollow fibers. This novel method necessitates the use of a semiconductor and an appropriate light source. When blood interacts with a semiconductor in the presence of light, it produces dissolved oxygen directly from the water found in the blood. In this study, we introduce a photocatalyst referred to as surface modified TiO2 nanotubes combined with Ti3C2Tx MXene. Initially, TiO2 nanotubes were fabricated using an electrochemical anodization process. Following this, Ti3C2Tx flakes were applied to the surface of the TNTs through a chemical bath technique. The Ti3C2Tx-TNTs samples were characterized using X-ray diffraction (XRD), field emission scanning electron microscope (FE-SEM), High-Resolution Transmission Electron Microscope (HRTEM), and X-ray photoelectron spectroscope (XPS). The hemolysis activity was evaluated to assess the biocompatibility of the produced samples. In terms of blood oxygenation, the Ti3C2Tx-TNTs are simply placed in contact with blood and then exposed to a UV lamp to initiate the photocatalytic reaction. Optical absorption studies on diluted blood demonstrate a significant enhancement in blood oxygenation. The absorption value at 415 nm, which corresponds to the oxyhemoglobin peak, shows a relative increase in oxygenation values from 2.08 (bare TNTs) to 2.84 (Ti3C2Tx-TNTs), significantly due to the formation of a Schottky barrier between MXene and TNTs. This positive change is also reflected in the standard hemoglobin test, with levels increasing from 16.7 (bare TNTs) to 17.9 g/dL (Ti3C2Tx-TNTs). An examination of the structure of red blood cells was conducted using an optical microscope, and it was observed that there was no occurrence of hemolysis after the photocatalytic process.