State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, Beijing 100029, China.
Talanta. 2012 Jan 30;89:142-8. doi: 10.1016/j.talanta.2011.12.004. Epub 2011 Dec 8.
In this work, we utilize the triangular gold nanoparticles (AuNPs) prepared by trisodium citrate reduction of HAuCl(4) in presence of nonionic fluorosurfactant (FSN) as a novel chemiluminescence (CL) probe for the determination of captopril. Captopril can induce a sharp decrease in CL intensity from the triangular AuNPs-catalyzed luminol system. Under the selected experimental conditions, a linear relationship was obtained between the logarithm of CL intensity and the logarithm of concentration of captopril in the range of 23.0-920 nM, and the detection limit at a signal-to-noise ratio of 3 for captopril was 4.6 nM. The as-prepared triangular AuNPs were easier to synthesize, stable at a wider pH range and high ionic strength, and exhibited a high selectivity and an excellent sensitivity toward captopril. The applicability of the proposed method has been validated by determining captopril in commercial pharmaceutical formulations and human urine samples with satisfactory results. The recoveries for captopril in spiked samples were found to be between 95.0% and 103.5%. The method shows promise for routine control analysis of pharmaceutical preparations and human urine samples. Moreover, based on the CL spectra, UV-vis spectra and transmission electron microscope (TEM) measurements, a possible CL mechanism was proposed. The mechanism of high selectivity toward captopril is supposed to originate from the tight binding of the sulphydryl groups of captopril to the active site of the as-prepared triangular AuNPs, leading to oxygen-related radicals cannot easily be generated from H(2)O(2) on the surface of triangular AuNPs.
在这项工作中,我们利用柠檬酸三钠还原 HAuCl(4)并在非离子氟表面活性剂 (FSN) 存在下制备的三角形金纳米粒子 (AuNPs) 作为一种新的化学发光 (CL) 探针,用于测定卡托普利。卡托普利可以诱导三角形 AuNPs 催化鲁米诺体系的 CL 强度急剧下降。在选定的实验条件下,CL 强度的对数与卡托普利浓度的对数在 23.0-920 nM 范围内呈线性关系,卡托普利的检测限为 3 倍信噪比时为 4.6 nM。所制备的三角形 AuNPs 更容易合成,在更宽的 pH 范围和高离子强度下稳定,对卡托普利表现出高选择性和优异的灵敏度。该方法已通过测定商业药物制剂和人尿样中的卡托普利得到验证,结果令人满意。在加标样品中,卡托普利的回收率在 95.0%至 103.5%之间。该方法有望用于药物制剂和人尿样的常规控制分析。此外,根据 CL 光谱、紫外-可见光谱和透射电子显微镜 (TEM) 测量,提出了一种可能的 CL 机制。对卡托普利具有高选择性的机制可能源于卡托普利的巯基与所制备的三角形 AuNPs 的活性位点的紧密结合,导致表面的 H(2)O(2) 上不易产生与氧相关的自由基三角形 AuNPs。