Bovine serum albumin functionalized blue emitting Ti 3 C 2 MXene quantum dots as a sensitive fluorescence probe for Fe 3+ ion detection and its toxicity analysis.
Mohammed Ali Al-DuaisZuhair M MohammedsalehHamza S Al-ShehriYahya S Al-AwthanSuhair A Bani-AttaAli A KeshkSyed Khalid MustafaAdel D AlthaqafyJozaa N Al-TweherHatem A Al-AohPanneerselvam ChellasamyPublished in: Luminescence : the journal of biological and chemical luminescence (2022)
In the present work, an improved class of protein functionalized fluorescent 2D Ti 3 C 2 MXene quantum dots (MXene QDs) was prepared using a hydrothermal method. Exfoliated 2D Ti 3 C 2 sheets were used as the starting precursor and transport protein bovine serum albumin (BSA) was used to functionalize the MXene QDs. BSA-functionalized MXene QDs exhibited excellent photophysical property and stability at various physiological parameters. High-resolution transmission electron microscopy analysis showed that the BSA@MXene QDs were quasispherical in shape with a size of ~2 nm. The fluorescence intensity of BSA@MXene QDs was selectively quenched in the presence of Fe 3+ ions. The mechanism of fluorescence quenching was further substantiated using time-resolved fluorescence and Stern-Volmer analysis. The sensing assay showed a linear response within the concentration range 0-150 μM of Fe 3+ ions with excellent limit of detection. BSA@MXene QDs probe showed good selectivity toward ferric ions even in the presence of other potential interferences. The practical applicability of BSA@MXene QDs was further tested in real samples for Fe 3+ ion quantification and the sensor had good recovery rates. The cytotoxicity studies of the BSA@MXene QDs toward the human glioblastoma cells revealed that BSA@MXene QDs are biocompatible at lower doses and showed significant cytotoxicity at higher dosages.
Keyphrases
- quantum dots
- energy transfer
- sensitive detection
- single molecule
- high resolution
- endothelial cells
- cell proliferation
- mass spectrometry
- aqueous solution
- risk assessment
- binding protein
- living cells
- loop mediated isothermal amplification
- cell cycle arrest
- signaling pathway
- label free
- induced apoptosis
- pi k akt
- liquid chromatography
- climate change
- drug release
- molecularly imprinted
- fluorescent probe