| Literature DB >> 35102681 |
Mohammed Ali Al-Duais1,2, Zuhair M Mohammedsaleh3, Hamza S Al-Shehri4, Yahya S Al-Awthan5,6, Suhair A Bani-Atta7, Ali A Keshk7, Syed Khalid Mustafa7, Adel D Althaqafy7, Jozaa N Al-Tweher7, Hatem A Al-Aoh7, Chellasamy Panneerselvam5.
Abstract
In the present work, an improved class of protein functionalized fluorescent 2D Ti3 C2 MXene quantum dots (MXene QDs) was prepared using a hydrothermal method. Exfoliated 2D Ti3 C2 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 Fe3+ 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 Fe3+ 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 Fe3+ 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.Entities:
Keywords: BSA@MXene QDs; Fe3+ ions; fluorescence detection; human glioblastoma cells; toxicity
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Year: 2022 PMID: 35102681 DOI: 10.1002/bio.4204
Source DB: PubMed Journal: Luminescence ISSN: 1522-7235 Impact factor: 2.464