Key Laboratory for Space Bioscience and Biotechnology, School of Life Sciences, Northwestern Polytechnical University, Xi'an, Shaanxi, 710072, China.
College of Chemistry and Chemical Engineering, Xi'an University of Science and Technology, Xi'an, Shaanxi, 710054, China.
Mikrochim Acta. 2022 Jan 24;189(2):70. doi: 10.1007/s00604-022-05175-y.
A colorimetric assay based on polydiacetylenes (PDA) nano-liposomes is reported for facile and sensitive detection of alkaline phosphatase (ALP) activity. The critical basis of this method is that the interaction of pyridoxal phosphate (PLP) with nitrogenous group functionalized PDA nano-liposomes induces distinct blue-to-red color changes of PDA nano-liposomes. In the presence of ALP, as a nature substrate, PLP is enzymatically hydrolyzed to form pyridoxal, which cannot interact with PDA nano-liposomes. As a result, the concentration of PLP is reduced and the color change of PDA nano-liposomes is retarded, which is associated with ALP level. Under optimal conditions, the proposed method showed good linear relationship with ALP activity in the range 10-200 U/L with a limit of detection of 2.8 U/L. The detection process could be vividly observed with the naked eye. Additional attempts by using the method for the evaluation of inhibitor efficiency were also achieved with satisfying results. The method was further challenged with real human serum samples, showing consistent results when compared with a commercial standard assay kit. Such simple and easy-to-use approach may provide a new alternative for clinical and biological detection of ALP.
基于聚二乙酰亚胺(PDA)纳米脂质体的比色法用于简便、灵敏地检测碱性磷酸酶(ALP)活性。该方法的关键基础是吡哆醛磷酸(PLP)与含氮基团功能化的 PDA 纳米脂质体的相互作用诱导 PDA 纳米脂质体发生明显的蓝-红颜色变化。在存在 ALP 作为天然底物的情况下,PLP 被酶促水解形成不能与 PDA 纳米脂质体相互作用的吡哆醛。结果,PLP 的浓度降低,PDA 纳米脂质体的颜色变化受到抑制,这与 ALP 水平相关。在最佳条件下,该方法在 10-200 U/L 的范围内与 ALP 活性呈良好的线性关系,检测限为 2.8 U/L。检测过程可以用肉眼生动地观察到。此外,还尝试使用该方法评估抑制剂效率,结果令人满意。该方法进一步应用于真实的人血清样本,与商业标准检测试剂盒相比,结果一致。这种简单易用的方法可能为 ALP 的临床和生物学检测提供新的选择。