Quintana José Benito, Miró Manuel, Estela José Manuel, Cerdà Víctor
Department of Water Quality Control, Technical University of Berlin, Sekr KF 4, Strasse des 17 Juni 135, D-10623 Berlin, Germany.
Anal Chem. 2006 Apr 15;78(8):2832-40. doi: 10.1021/ac052256z.
In this paper, the third generation of flow injection analysis, also named the lab-on-valve (LOV) approach, is proposed for the first time as a front end to high-performance liquid chromatography (HPLC) for on-line solid-phase extraction (SPE) sample processing by exploiting the bead injection (BI) concept. The proposed microanalytical system based on discontinuous programmable flow features automated packing (and withdrawal after single use) of a small amount of sorbent (<5 mg) into the microconduits of the flow network and quantitative elution of sorbed species into a narrow band (150 microL of 95% MeOH). The hyphenation of multisyringe flow injection analysis (MSFIA) with BI-LOV prior to HPLC analysis is utilized for on-line postextraction treatment to ensure chemical compatibility between the eluate medium and the initial HPLC gradient conditions. This circumvents the band-broadening effect commonly observed in conventional on-line SPE-based sample processors due to the low eluting strength of the mobile phase. The potential of the novel MSFI-BI-LOV hyphenation for on-line handling of complex environmental and biological samples prior to reversed-phase chromatographic separations was assessed for the expeditious determination of five acidic pharmaceutical residues (viz., ketoprofen, naproxen, bezafibrate, diclofenac, and ibuprofen) and one metabolite (viz., salicylic acid) in surface water, urban wastewater, and urine. To this end, the copolymeric divinylbenzene-co-n-vinylpyrrolidone beads (Oasis HLB) were utilized as renewable sorptive entities in the micromachined unit. The automated analytical method features relative recovery percentages of >88%, limits of detection within the range 0.02-0.67 ng mL(-1), and coefficients of variation <11% for the column renewable mode and gives rise to a drastic reduction in operation costs ( approximately 25-fold) as compared to on-line column switching systems.
本文首次提出将第三代流动注射分析,即阀上实验室(LOV)方法,作为高效液相色谱(HPLC)的前端,通过利用珠进样(BI)概念进行在线固相萃取(SPE)样品处理。所提出的基于不连续可编程流动的微分析系统具有以下特点:将少量吸附剂(<5 mg)自动填充(单次使用后取出)到流动网络的微导管中,并将吸附物质定量洗脱到窄带(150 μL 95%甲醇)中。在HPLC分析之前,将多注射器流动注射分析(MSFIA)与BI-LOV联用进行在线萃取后处理,以确保洗脱液介质与初始HPLC梯度条件之间的化学兼容性。这避免了传统在线SPE样品处理器中常见的由于流动相洗脱强度低而导致的谱带展宽效应。评估了新型MSFI-BI-LOV联用在反相色谱分离之前在线处理复杂环境和生物样品的潜力,用于快速测定地表水、城市废水和尿液中的五种酸性药物残留(即酮洛芬、萘普生、苯扎贝特、双氯芬酸和布洛芬)和一种代谢物(即水杨酸)。为此,将共聚二乙烯基苯-共-n-乙烯基吡咯烷酮珠(Oasis HLB)用作微加工单元中的可再生吸附实体。该自动分析方法的特点是相对回收率>88%,检测限在0.02 - 0.67 ng mL⁻¹范围内,柱可再生模式下变异系数<11%,与在线柱切换系统相比,运行成本大幅降低(约25倍)。