Abstract

A N-doped carbon dot (NCD) has been synthesized via a simplistic one-step hydrothermal technique using l-aspartic acid and 3,6-diaminoacridine hydrochloride. The NCDs exhibit a high quantum yield (22.7%) and excellent optical stability in aqueous media. Additionally, NCDs display good solid-state yellowish-green emission and are suitable for security ink applications. The remarkable fluorescence (FL) properties of NCDs are further applied to develop a multifunctional sensor for bilirubin (BR) and vitamin B12 (VB12) via fluorescence quenching. We have systematically studied the FL quenching mechanisms of the two analytes. The primary quenching mechanism of BR is via the Förster resonant energy transfer (FRET) pathway facilitated by the H-bonding network between the hydrophilic moieties existing at the surface of BR and NCDs. In contrast, the inner filter effect (IFE) is mainly responsible for the recognition of VB12. The practicability of the nanoprobe NCDs is further tested in real-sample analysis for BR (human serum and urine samples) and VB12 (VB12 tablets, human serum, and energy drink) with a satisfactory outcome. The in vitro competency is also verified in the human cervical cancer cell line (HeLa cell) with negligible cytotoxicity and significant biocompatibility. This result facilitates the application of NCDs for bioimaging and recognition of VB12 in a living organism.

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