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采用流动注射化学发光分析法连续定量监测人唾液中的罗红霉素。

Continuous, quantitative monitoring of roxithromycin in human saliva by flow injection chemiluminescence analysis.

机构信息

Key Laboratory of Synthetic and Natural Functional Molecule, Chemistry of Ministry of Education, College of Chemistry and Material Science, Northwest University, Xi'an 710069, China.

出版信息

Appl Spectrosc. 2013 Jan;67(1):54-8. doi: 10.1366/12-06644.

Abstract

Human saliva quantitative monitoring of roxithromycin (ROX) at picomolar-level by flow injection (FI) chemiluminescence (CL) analysis is described for the first time, to our knowledge. Monitoring was based on the CL intensity from luminol-BSA reaction, which can be quenched in the presence of ROX, with the decreasing CL intensity linearly proportional to the logarithm of the ROX concentration, ranging from 0.6 to 1000 pmol·L(-1). The detection limit of the proposed method for the determination of ROX was as low as 0.2 pmol·L(-1) (3σ), and the relative standard deviations were less than 4.0% (n = 7). A complete analytical process, including sampling and washing for ROX determination, conducted at a flow rate of 2.0 mL·min(-1), was performed completely within 30 s, yielding a sample efficiency of 120 h(-1). The proposed method was successfully applied to the determination of ROX in human saliva and serum samples with recoveries from 90.9% to 110.1%. The continuous monitoring of ROX in human saliva after oral intake showed that the total elimination ratio was 87.1% during 24 h, and the pharmacokinetic parameters were 0.97 ± 0.18 h(-1) for the absorption rate constant K(a), 0.082 ± 0.010 h(-1) for the elimination rate constant K(e), and 8.56 ± 1.11 h for the elimination half-life time t(1/2). It was also found that ROX in human saliva and urine simultaneously reached the maximum at 2 h with the concentration correlate ratio of 0.97.

摘要

首次描述了通过流动注射(FI)化学发光(CL)分析在皮摩尔级定量监测人唾液中罗红霉素(ROX)的方法。监测基于洛氨酸-BSA 反应的 CL 强度,在 ROX 存在下,该反应的 CL 强度会被猝灭,CL 强度的降低与 ROX 浓度的对数呈线性关系,范围为 0.6 至 1000 pmol·L(-1)。该方法对 ROX 的检测限低至 0.2 pmol·L(-1)(3σ),相对标准偏差小于 4.0%(n = 7)。在 2.0 mL·min(-1)的流速下,包括用于 ROX 测定的采样和洗涤在内的完整分析过程在 30 秒内完全完成,样品效率为 120 h(-1)。该方法成功应用于人唾液和血清样品中 ROX 的测定,回收率为 90.9%至 110.1%。口服后连续监测人唾液中的 ROX 表明,24 小时内总消除率为 87.1%,药代动力学参数为吸收速率常数 K(a)为 0.97 ± 0.18 h(-1),消除速率常数 K(e)为 0.082 ± 0.010 h(-1),消除半衰期 t(1/2)为 8.56 ± 1.11 h。还发现人唾液和尿液中的 ROX 同时在 2 小时达到最大值,浓度相关比为 0.97。

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