J Chromatogr A. 2013 Nov 29;1318:49-57. doi: 10.1016/j.chroma.2013.10.022.
tIn this work, polyethyleneglycol (PEG)/hydroxyl polydimethylsiloxane (OH-PDMS)/γ -mercaptopropyltrimethoxysilane (γ -MPTS) coated stir bar was prepared by sol–gel process and its extraction performance for the extraction of amphoteric thyroxines (3,3',5,5'-tetraiodothyronin, T(4); 3,3',5-triiodothyronine, T(3); reversed-3,3',5-triiodothyronine, rT(3)) and their metabolite (3,5-diiodothyronine,T2) was studied. The preparation reproducibility of PEG/OH-PDMS/γ -MPTS coated stir bar was investigated, and the relative standard deviations (RSDs) in the same batch and among different batches were 3.3–14.3% (n = 5) and 7.7–16.6% (n = 3), respectively. The prepared PEG/OH-PDMS/γ -MPTS coated stir bar could be reused for more than 20 times. Based on this fact, a novel method of stir bar sorptive extraction (SBSE) combined with high performance liquid chromatography (HPLC)-ultraviolet (UV)and HPLC-inductively coupled plasma mass spectrometry (ICP-MS) for the analysis of target thyroxinesin human urine samples was developed. The influencing factors of SBSE, such as sample pH, extraction time, stirring rate, salt effect, desorption solution and desorption time, were studied in detail, and the analytical performance of the proposed method was evaluated under the optimized conditions. The enrichment factors (EFs) of the developed method for four target thyroxines were in the range of 14.9–70.4(theoretical enrichment factor was 100). The RSDs were ranging from 4.0% to 13.8% for SBSE-HPLC-UV (c = 25 μg/L, n = 6) and from 3.7% to 6.1% for SBSE-HPLC-ICP-MS (c = 0.5 μg/L, n = 5). The linear range obtained by SBSE-HPLC-UV was 2–500 μg/L for T(2)and 5–500 μg/L for rT3, T(3)and T(4), with correlation coefficients (r) ranging from 0.9957 to 0.9998, respectively, while the linear range obtained by SBSE-HPLC-ICP-MS was 0.05–500 μg/L for T(2) and rT(3), 0.10–200 μg/L for T(3) and 0.05–200 μg/L for T(4)with r ranging from 0.9979 to 0.9998, respectively. The limits of detection (LODs) for the target thyroxines were 0.60–2.20 μg/L for SBSE-HPLC-UV and 0.0071–0.0355 μg/L SBSE-HPLC-ICP-MS, respectively. The developed method was applied for the determination of target thyroxines in urine samples, and the recovery for the spiking samples obtained by SBSE-HPLC-UV was in the range of 81.6–137.6% for human urine,while the recovery for the spiking urine samples obtained by SBSE-HPLC-ICP-MS were in the range of 72.0–121.5%.
在这项工作中,通过溶胶-凝胶法制备了聚乙二醇(PEG)/羟基聚二甲基硅氧烷(OH-PDMS)/γ -巯丙基三甲氧基硅烷(γ -MPTS)涂层搅拌棒,并研究了其对两性甲状腺素(3,3',5,5'-四碘甲状腺原氨酸,T(4);3,3',5-三碘甲状腺原氨酸,T(3);反向-3,3',5-三碘甲状腺原氨酸,rT(3))及其代谢物(3,5-二碘甲状腺素,T2)的萃取性能。考察了 PEG/OH-PDMS/γ -MPTS 涂层搅拌棒的制备重现性,同一批次和不同批次的相对标准偏差(RSD)分别为 3.3%-14.3%(n=5)和 7.7%-16.6%(n=3)。制备的 PEG/OH-PDMS/γ -MPTS 涂层搅拌棒可重复使用 20 多次。基于这一事实,开发了一种基于搅拌棒吸附萃取(SBSE)结合高效液相色谱(HPLC)-紫外(UV)和高效液相色谱-电感耦合等离子体质谱(ICP-MS)分析人尿液中目标甲状腺素的新方法。详细研究了 SBSE 的影响因素,如样品 pH 值、萃取时间、搅拌速度、盐效应、解吸溶液和解吸时间,并在优化条件下评价了所提出方法的分析性能。该方法对四种目标甲状腺素的富集因子(EFs)范围为 14.9-70.4(理论富集因子为 100)。SBSE-HPLC-UV(c=25μg/L,n=6)的 RSD 范围为 4.0%-13.8%,SBSE-HPLC-ICP-MS(c=0.5μg/L,n=5)的 RSD 范围为 3.7%-6.1%。SBSE-HPLC-UV 的线性范围为 T(2)2-500μg/L,rT3、T(3)和 T(4)为 5-500μg/L,相关系数(r)分别为 0.9957-0.9998,而 SBSE-HPLC-ICP-MS 的线性范围为 T(2)0.05-500μg/L 和 rT(3),T(3)0.10-200μg/L 和 T(4)0.05-200μg/L,r 分别为 0.9979-0.9998。目标甲状腺素的检出限(LOD)为 SBSE-HPLC-UV 为 0.60-2.20μg/L,SBSE-HPLC-ICP-MS 为 0.0071-0.0355μg/L。该方法用于测定人尿液中目标甲状腺素的含量,通过 SBSE-HPLC-UV 测定的加标样品的回收率在 81.6%-137.6%之间,而通过 SBSE-HPLC-ICP-MS 测定的加标尿液样品的回收率在 72.0%-121.5%之间。