Issue 12, 2021, Issue in Progress

Construction of a ratio fluorescence assay of 5-aminosalicylic acid based on its aggregation induced emission with blue emitting N/P-codoped carbon dots

Abstract

Herein, a novel ratio fluorescence method based on N/P-doped carbon dots (NPCDs) for detecting 5-aminosalicylic acid (5-ASA) in mesalazine enteric coated tablets and blood were reported for the first time. NPCDs were successfully prepared through a simple one-step hydrothermal strategy by employing adenosine triphosphate (ATP) and p-toluidine as raw materials. NPCDs exhibit bright blue emissions with excitation/emission peaks at 340/423 nm with moderate quantum yield (20.75%). In addition, 5-ASA has a certain weak fluorescence emission peak at 487 nm. Adding 5-ASA into NPCDs significantly enhanced the fluorescence intensity, which may result from aggregation induced emission (AIE) of 5-ASA on the surface of NPCDs. Therefore, NPCDs only provide self-calibration signals, and their fluorescence remains almost unchanged when co-existing with 5-ASA. Therefore, the ratio of fluorescence at F487/F423 was used for detection of 5-ASA. For the fluorometric determination assay, there was a good linear relationship between F487/F423 and 5-ASA concentration between 0.50 and 130 μM (R2 = 0.9979). The detection limit was about 0.13 μM. Therefore, this method is simple, sensitive and low cost, and will be successfully applied to the detection of 5-ASA in drugs.

Graphical abstract: Construction of a ratio fluorescence assay of 5-aminosalicylic acid based on its aggregation induced emission with blue emitting N/P-codoped carbon dots

Supplementary files

Article information

Article type
Paper
Submitted
05 Dec 2020
Accepted
26 Jan 2021
First published
10 Feb 2021
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2021,11, 6607-6613

Construction of a ratio fluorescence assay of 5-aminosalicylic acid based on its aggregation induced emission with blue emitting N/P-codoped carbon dots

Y. Hu, Y. Wang, R. Guan, C. Zhang, X. Shao and Q. Yue, RSC Adv., 2021, 11, 6607 DOI: 10.1039/D0RA10258J

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