Zhang Qiulin, Chen Beibei, He Man, Hu Bin
Department of Chemistry, Wuhan University, Wuhan 430072, China.
Department of Chemistry, Wuhan University, Wuhan 430072, China.
Anal Chim Acta. 2024 Dec 1;1331:343332. doi: 10.1016/j.aca.2024.343332. Epub 2024 Oct 11.
Traditional blood drug analysis involves large blood consumption and complicated operations and a further reduction in blood consumption is urgently needed. Chip-based monolithic column microextraction is a good strategy for the pretreatment of small-volume samples, and new monolithic materials is the critical factor. Covalent organic frameworks (COFs) are good adsorbents due to large specific surface area and rich conjugated structure. However, the poor dispersion ability of COFs in prepolymer solution severely hinders the preparation of COFs doped monolithic columns. Herein, high internal phase emulsion with viscoelastic properties was adopted to fixed COF particles.
The COFs doped monolith exhibited a hierarchical porous structure and improved extraction efficiency for interest nonsteroidal anti-inflammatory drugs (NSAIDs) (68.2-77.3 vs 28.4-57.7 %). A chip-based monolithic column array was fabricated and coupled with high-performance liquid chromatography (HPLC)-ultraviolet detection for online determination of five NSAIDs in microlitre volume of blood. The throughput of the developed method was approximately 3 h, mainly determined by the separation time (22 min) of target NSAIDs in HPLC. Under the optimal conditions (200 μL sample solution, pH = 3 at a sampling folw rate of 5 μL min and 20 μL of acetonitrile/10 mmol L NaOH (9/1, v/v) as desorbent), the detection limit of 4.39-15.5 μg L was obtained for target NSAIDs in blood with RSD of 7.8-15.3 % and R of 0.9943-0.9978. The method was applied to the analysis of human serum (20 μL) and dried blood spot, with recovery of 82.0-118 % for target NSAIDs.
A method was proposed for the preparation of COF doped monolithic columns by emulsion polymerization, avoiding uneven distribution of COFs caused by their easy sedimentation in traditional free radical preparation of monolithic columns. Then a chip-based monolithic column array coupled with on-line HPLC-UV detection was established for the quantification of five NSAIDs in microlitre-blood samples. The developed method merits high automation and good anti-interference ability, with extremely low sample/reagents consumption.
传统的血液药物分析需要大量的血液消耗和复杂的操作,因此迫切需要进一步减少血液消耗。基于芯片的整体柱微萃取是一种用于小体积样品预处理的好策略,而新型整体材料是关键因素。共价有机框架(COFs)由于具有较大的比表面积和丰富的共轭结构,是良好的吸附剂。然而,COFs 在预聚物溶液中的分散能力差严重阻碍了 COFs 掺杂整体柱的制备。在此,采用具有粘弹性的高内相乳液固定 COF 颗粒。
COFs 掺杂的整体柱呈现分级多孔结构,并提高了对目标非甾体抗炎药(NSAIDs)(68.2-77.3% 与 28.4-57.7%)的萃取效率。制备了基于芯片的整体柱阵列,并与高效液相色谱(HPLC)-紫外检测联用,用于微升体积血液中五种 NSAIDs 的在线测定。该方法的通量约为 3 小时,主要由 HPLC 中目标 NSAIDs 的分离时间(22 分钟)决定。在最佳条件下(200 μL 样品溶液,pH = 3,采样流速为 5 μL/min,20 μL 乙腈/10 mmol/L NaOH(9/1,v/v)作为洗脱液),该方法对血液中目标 NSAIDs 的检测限为 4.39-15.5 μg/L,RSD 为 7.8-15.3%,R 为 0.9943-0.9978。该方法用于分析人血清(20 μL)和干血斑,目标 NSAIDs 的回收率为 82.0-118%。
提出了一种通过乳液聚合制备 COF 掺杂整体柱的方法,避免了 COFs 在传统自由基制备整体柱过程中因易沉降而导致的分布不均匀。然后建立了基于芯片的整体柱阵列,与在线 HPLC-UV 检测联用,用于微升血液样品中五种 NSAIDs 的定量分析。该方法自动化程度高,抗干扰能力强,样品/试剂消耗量极低。