4.6 Article

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

Journal

RSC ADVANCES
Volume 11, Issue 12, Pages 6607-6613

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d0ra10258j

Keywords

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Funding

  1. Natural Science Foundation of China [91543206]
  2. Natural Science Foundation [ZR2014BQ017, ZR2015BM024, 2013SJGZ07]
  3. Tai-Shan Scholar Research Fund of Shandong Province and research foundation of Liaocheng University

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A novel ratio fluorescence method based on NPCDs for detecting 5-ASA in drugs was reported, showing simplicity, sensitivity, and low cost. The method relies on the measurement of F-487/F-423 fluorescence ratio for quantifying 5-ASA concentration, with a good linear relationship and low detection limit.
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 F-487/F-423 was used for detection of 5-ASA. For the fluorometric determination assay, there was a good linear relationship between F-487/F-423 and 5-ASA concentration between 0.50 and 130 mu M (R-2 = 0.9979). The detection limit was about 0.13 mu M. Therefore, this method is simple, sensitive and low cost, and will be successfully applied to the detection of 5-ASA in drugs.

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