AI Article Synopsis

  • MXene is a novel 2D material known for its high surface area, conductivity, and strength, used in detecting anti-cancer drugs, while bismuth vanadate (BiVO) is non-toxic but can cause irritation when loaded onto stem cells.
  • The study focuses on fabricating titanium carbide (TiC)-BiVO nanomaterials combined with oxides for targeted anti-cancer applications, utilizing X-ray diffraction (XRD) and scanning electron microscopy (SEM) for assessment.
  • The preparation involved dissolving titanium aluminum carbide (TiAlC) in hydrofluoric acid and using a magnetic stirring system for efficient etching, followed by synthesis of BiVO through a hydrothermal method.

Article Abstract

Background MXene is a newly discovered substance consisting of 2D transition metal carbides or nitrides, produced through the disintegration and etching of aluminum layers. It possesses numerous properties, including a high surface area, conductivity, strength, stiffness, negative zeta potential, and excellent volumetric capacitance. MXene is utilized in detecting anti-cancer medicine, while bismuth vanadate (BiVO) is synthesized to form an optimized material for anti-cancer activity applications. BiVO exhibits visible light absorption, strong chemical stability, and non-toxic properties. However, when loaded onto target stem cells, it can cause skin and respiratory irritation. Aim This study aimed to evaluate the facile fabrication of titanium carbide (TiC)-BiVO nanomaterials coupled with oxides for anti-cancer activity. Moreover, it aimed to create TiC-BiVO nanomaterials in combination with oxides using X-ray diffraction (XRD) and scanning electron microscopy (SEM) to assess their potential as efficient and targeted anti-cancer agents. Methods and materials To prepare the 2D TiC MXene, 2.5 g of titanium aluminum carbide (TiAlC) powder was dissolved in 60 mL of a 40% hydrofluoric acid (HF) solution in a polytetrafluoroethylene(PTFE) container. The etching process was made more efficient and completed in 24 hours by using a magnetic stirring system to keep the mixture stirred and heated continuously. The centrifugation was performed at 4000 rpm for five minutes. Subsequently, deionized water was used to wash the solution many times until its pH reached around 7. The appropriate TiC powder was made by vacuum drying the acquired sediment at 80°C for 24 hours. Monoclinic BiVO samples were synthesized via a hydrothermal method. Typically, 10 mmol of Bi(NO).5HO was dissolved in 100 mL of a 2 mol/L HNO solution and stirred uniformly. Subsequently, 10 mmol of ammonium metavanadate (NHVO) was added to the mixed solution. After being stirred for one hour, the mixture was transferred into a 100 mL sealed Teflon-lined stainless steel autoclave at 180°C for 16 hours. After cooling to room temperature, the sediment was washed three times with deionized water, ethanol, and acetone, respectively. Finally, the suspension was dried at 80°C, followed by calcination at 450°C for three hours to obtain BiVO. TiC-BiVO heterostructures were prepared by surface modification TiCusing BiVO suspensions by a simple, cost-effective approach. Results TiC nanosheets were observed with BiVO particles, and the high crystalline nature of the compound was confirmed after XRD analysis and energy-dispersive spectroscopy (EDS) analysis. The compound was found to be pure without any impurities and exhibited anti-cancer activity. Conclusion The XRD, field emission scanning electron microscopy(FESEM), and EDS investigations provide an in-depth analysis of the structural, morphological, and compositional characteristics of TiC-BiVO sheets. The XRD analysis proves the successful combination of different materials and the presence of crystalline phases. The FESEM imaging technique exposes the shape and arrangement of particles in sheets, while the EDS analysis verifies the elemental composition and uniform distribution. These investigations show that TiC-BiVO composites have been successfully synthesized, indicating their potential for use in anti-cancer applications.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11216123PMC
http://dx.doi.org/10.7759/cureus.61492DOI Listing

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