Guangxi Key Laboratory of Electrochemical and Magnetochemical Function Materials, College of Chemistry and Bioengineering, Guilin University of Technology, Guangxi, 541004, China.
Guangxi Key Laboratory of Electrochemical and Magnetochemical Function Materials, College of Chemistry and Bioengineering, Guilin University of Technology, Guangxi, 541004, China.
Anal Chim Acta. 2024 Feb 8;1289:342210. doi: 10.1016/j.aca.2024.342210. Epub 2024 Jan 3.
Alkaline phosphatase (ALP) is a major biomarker for clinical diagnosis, but detection methods of ALP are limited in sensitivity and selectivity. In this paper, a novel method for ALP determination is proposed. A photoelectrochemical (PEC) sensor was prepared by growing UiO-tetratopic tetrakis (4-carbox-yphenyl) porphyrin (TCPP) in situ between layered TiC through a one-pot hydrothermal method. The obtained Schottky heterojunction photoelectric material TiC@UiO-TCPP not only has a large light absorption range but also greatly improves the efficiency of photogenerated electron hole separation and thereby enhances sensitivity for PEC detection. The phosphate group on the phosphorylated polypeptide was utilized to form a Zr-O-P bond with the zirconium ion on UiO-66, and then photocurrent decreases due to the steric hindrance effect of phosphorylated polypeptides, that is, the hindrance of electron transfer between the photoelectric material and a solution. The specific interaction between ALP and phosphorylated polypeptides shears the bond between phosphate and zirconium ion on UiO-66 in the peptides then weakens the hindrance effect and increases the photocurrent, thus realizing ALP detection. The linear range of ALP is 0.03-10,000 U·L, and the detection limit is 0.012 U·L. The method is highly sensitive and selective, and has been applied in detection of ALP in serum samples.
碱性磷酸酶(ALP)是临床诊断的主要生物标志物,但 ALP 的检测方法在灵敏度和选择性方面受到限制。本文提出了一种新的 ALP 测定方法。通过一锅水热法在层状 TiC 之间原位生长四配位四(4-羧基苯基)卟啉(TCPP),制备了光电化学(PEC)传感器。所得的肖特基异质结光电材料 TiC@UiO-TCPP 不仅具有较大的光吸收范围,而且还极大地提高了光生电子空穴分离的效率,从而提高了 PEC 检测的灵敏度。磷酸化多肽上的磷酸基团与 UiO-66 上的锆离子形成 Zr-O-P 键,然后由于磷酸化多肽的空间位阻效应,光电流减小,即光电材料和溶液之间电子转移的阻碍。ALP 与磷酸化多肽之间的特异性相互作用剪切了多肽中磷酸和锆离子之间的键,从而减弱了阻碍效应并增加了光电流,从而实现了 ALP 的检测。ALP 的线性范围为 0.03-10000 U·L,检测限为 0.012 U·L。该方法灵敏度高、选择性好,已应用于血清样品中 ALP 的检测。