Herein, a novel magnetic relaxation sensing strategy based on the change in Fe3+ content has been proposed by utilizing the conversion of Fe3+ ions to Prussian blue (PB) precipitates. Compared with the common detection approach based on the valence state change of Fe3+ ions, our strategy can cause a larger change in the relaxation time of water protons and higher detection sensitivity since PB precipitate can induce a larger change in the Fe3+ ion concentration and has a weaker effect on the relaxation process of water protons relative to Fe2+ ions. Then, we employ alkaline phosphatase (ALP) as a model target to verify the feasibility and detection performance of the as-proposed strategy. Actually, ascorbic acid (AA) generated from the ALP-catalyzed L-ascorbyl-2-phosphate hydrolysis reaction can reduce potassium ferricyanide into potassium ferrocyanide, and potassium ferrocyanide reacts with Fe3+ to form PB precipitates, leading to a higher relaxation time. Under optimum conditions, the method for ALP detection has a wide linear range from 5 to 230 mU/mL, and the detection limit is 0.28 mU/mL, sufficiently demonstrating the feasibility and satisfactory analysis performance of this strategy, which opens up a new path for the construction of magnetic relaxation sensors. Furthermore, this strategy has also been successfully applied to ascorbic acid oxidase detection, suggesting its expansibility in magnetic relaxation detection.
Keywords: Alkaline phosphatase; Ascorbic acid oxidase; Fe(3+); Magnetic relaxation biosensing; Prussian blue; Signal amplification.
Copyright © 2023. Published by Elsevier B.V.