Chongqing Key Laboratory of Green Synthesis and Applications, College of Chemistry, Chongqing Normal University, Chongqing 401331, China.
Department of Pharmacy, the Second Affiliated Hospital of Chongqing Medical University, Chongqing 401331, China.
Molecules. 2023 Feb 16;28(4):1892. 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.
荧光银配位聚合物纳米粒子(Ag-TPA CPNs)是通过在 15 分钟内使用对苯二甲酸(TPA)和硝酸银的组合,通过超快速微波辅助策略合成的。Ag-TPA CPNs 的荧光量子产率(QY = 20.19%)和大斯托克斯位移(~200nm)较高,在 320nm 的激发波长下,有两个发射峰在 490nm 和 520nm。基于碱性磷酸酶(ALP)催化水解抗坏血酸 2-磷酸(AA2P)为抗坏血酸(AA),并将 AA 产物触发银离子还原为纳米银粒子,使用荧光 Ag-TPA CPNs 的荧光“关闭”方法来检测 ALP 活性。加入 ALP 后,Ag-TPA CPNs 的荧光寿命从 3.93ms 降低到 3.80ms,这表明这种荧光“关闭”检测 ALP 活性是一个动态猝灭过程。荧光强度与 ALP 浓度在 0.2-12mU/mL 范围内呈线性关系(r = 0.991),检测限(LOD)为 0.07mU/mL。它在检测 ALP 时对金属离子和氨基酸具有高度选择性,以及其他酶如辣根过氧化物酶、葡萄糖氧化酶、酪氨酸酶、胰蛋白酶、溶菌酶和超氧化物歧化酶。当它应用于血清样品中 ALP 活性的荧光“关闭”检测时,获得了 99.5%-101.2%的平均回收率,相对标准偏差(RSD)低于 4%的准确度。因此,它是分析生物样品中 ALP 水平的有效和准确工具。