Ultrarapid Microwave-Assisted Synthesis of Fluorescent Silver Coordination Polymer Nanoparticles and Its Application in Detecting Alkaline Phosphatase Activity

• Published in: Molecules (Basel, Switzerland) Vol. 28; no. 4; p. 1892
• Main Authors: Pei, Kanglin, Li, Di, Qi, Wenjing, Wu, Di
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 16.02.2023; MDPI
• Subjects: Acids; Alkaline phosphatase; Alkaline Phosphatase - metabolism; Ascorbic acid; ascorbic acid 2-phosphate; Coordination polymers; Enzymes; Fluorescence; Fluorescent Dyes - chemistry; fluorescent silver coordination polymer nanoparticles; Glucose oxidase; Horseradish peroxidase; Ligands; Limit of Detection; Lysozyme; Metal ions; Metal Nanoparticles - chemistry; microwave-assisted synthesis; Microwaves; Nanoparticles; Oxidases; Peroxidase; Phosphatase; Phosphatases; Polymer industry; Polymers; Selectivity; Silver; Superoxide; Terephthalic acid; Trypsin; Tyrosinase; China; ascorbic acid 2-phosphate; microwave-assisted synthesis; ascorbic acid; alkaline phosphatase; fluorescent silver coordination polymer nanoparticles
• ISSN: 1420-3049; 1420-3049
• DOI: 10.3390/molecules28041892

Fluorescent silver coordination polymer nanoparticles (Ag-TPA CPNs) were synthesized using a combination of terephthalic acid (TPA) and silver nitrate via an ultrarapid microwave-assisted strategy within 15 min. The Ag-TPA CPNs displayed a high fluorescent quantum yield (QY = 20.19%) and large Stokes shift (~200 nm), with two emission peaks at 490 nm and 520 nm under an excitation wavelength of 320 nm. A fluorescent "turn-off" method using fluorescent Ag-TPA CPNs was applied to detect the alkaline phosphatase (ALP) activity on the basis of the ALP-catalyzed hydrolysis of ascorbic acid 2-phosphate (AA2P) to ascorbic acid (AA), and the AA product triggered the reduction of Ag ions into silver nanoparticles. The fluorescent lifetime of Ag-TPA CPNs decreased from 3.93 ms to 3.80 ms after the addition of ALP, which suggests that this fluorescent "turn-off" detection of ALP activity is a dynamic quenching process. The fluorescent intensity had a linear relationship with the concentration of ALP in the range of 0.2-12 mU/mL (r = 0.991) and with a limit of detection (LOD) of 0.07 mU/mL. It showed high selectivity in ALP detection towards metal ions and amino acids, as well as other enzymes such as horseradish peroxidase, glucose oxidase, tyrosinase, trypsin, lysozyme, and superoxides. When it was applied for the fluorescent "turn-off" detection of ALP activity in serum samples, mean recovery levels ranging from 99.5% to 101.2% were obtained, with relative standard deviations (RSDs) lower than 4% accuracy. Therefore, it is an efficient and accurate tool for analyzing ALP levels in biosamples.