Ding Yanru, Zhang Nan, Zhao Junqi, Lv Haiyang, Wang Xu, Zhao Bing, Tian Yuan
College of Chemistry, Jilin Province Research Center for Engineering and Technology of Spectral Analytical Instruments, Jilin University, Changchun, 130012, People's Republic of China.
State Key Laboratory of Supramolecular Structure and Materials, Jilin University, Changchun, 130012, People's Republic of China.
Anal Bioanal Chem. 2022 Nov;414(27):7813-7822. doi: 10.1007/s00216-022-04315-w. Epub 2022 Sep 14.
In this paper, a surface-enhanced Raman scattering (SERS) strategy was constructed for the determination of antihypertensive drugs irbesartan (IRB) and doxazosin mesylate (DOX). β-Cyclodextrin-capped silver nanoparticles (CD-AgNPs) are employed as SERS-active substrate. The introduction of β-CD with hydrophobic cavity can capture drug molecules to form host-guest complex, making the drug molecules closer to the electromagnetic enhancement field of the AgNPs, thereby enhancing the SERS signal of drug molecules with low Raman cross-section. The vibrational modes of IRB and DOX are assigned by density functional theory calculations. The linear response from 3.0 × 10 to 1.0 × 10 mol L for IRB and 3.0 × 10 to 2.0 × 10 mol L for DOX and low limits of detection (LOD) 7.5 × 10 mol L for IRB and 8.6 × 10 mol L for DOX can be achieved. Meanwhile, this SERS approach can be applicable to determine IRB and DOX in commercial drug tablets, healthcare products, and human urine samples with recoveries of 90.8-115.7% and 90.0-113.5%, respectively, with relative standard deviation (RSD) less than 4.5%. This designed SERS strategy enables for the rapid determination of IRB and DOX in drug quality monitoring and illegal additives in healthcare products as well as clinical applications.
本文构建了一种表面增强拉曼散射(SERS)策略,用于测定抗高血压药物厄贝沙坦(IRB)和甲磺酸多沙唑嗪(DOX)。采用β-环糊精包覆的银纳米颗粒(CD-AgNPs)作为SERS活性基底。具有疏水空腔的β-CD的引入可以捕获药物分子形成主客体复合物,使药物分子更接近AgNPs的电磁增强场,从而增强拉曼截面较低的药物分子的SERS信号。通过密度泛函理论计算确定了IRB和DOX的振动模式。IRB的线性响应范围为3.0×10至1.0×10 mol/L,DOX为3.0×10至2.0×10 mol/L,检测限低,IRB为7.5×10 mol/L,DOX为8.6×10 mol/L。同时,这种SERS方法可用于测定商业药物片剂、保健品和人体尿液样本中的IRB和DOX,回收率分别为90.8-115.7%和90.0-113.5%,相对标准偏差(RSD)小于4.5%。这种设计的SERS策略能够在药物质量监测、保健品非法添加剂以及临床应用中快速测定IRB和DOX。