Liu Wei, Zhang Lan, Wei Zhenyi, Chen Shengping, Chen Guonan
The Sport Science Research Center, Ministry of Education Key Laboratory of Analysis and Detection for Food Safety, Fuzhou University, Fuzhou, Fujian 350002, China.
J Chromatogr A. 2009 Jul 10;1216(28):5340-6. doi: 10.1016/j.chroma.2009.05.040. Epub 2009 May 21.
A method using hollow fibre-protected liquid-phase microextraction (HF-LPME) with in situ derivatization followed by gas chromatography/mass spectrometry (GC/MS) was established for the analysis of beta-agonists and beta-blockers in urine. Because it can simultaneously extract and derivatize compounds of interest by methylbenzol and N-methyl-N-(trimethylsilyl) trifluoroacetamide (MSTFA) in HF-LPME, the approach overcomes the drawbacks of considerable time-consuming and tedious operation, meanwhile improves enrichment multiple. The optimized conditions were extraction for 20 min at 35 degrees C with 5.0 microL of mixed extraction solvent (methylbenzol/MSTFA=1:1, v/v) with stirring speed of 925 rpm in 5.0 mL sample under pH 12.0 and 14% (w/v) NaCl. The method provided very wide linear ranges (0.25-400 ng mL(-1)) and low detection limits in the range of 0.08-0.10 ng mL(-1) for clenbuterol, metoprolol and propranolol while enrichment factors reached up to 256. The analytes could be determined in spiked urine by the method with high extraction efficacy (93.79-109.04% recoveries) and precision (<9.70% RSD). It has a satisfactory result for metoprolol in practical human urine samples for a single-dose administration of 50 mg after 36 h. The proposed method only needs few microliters of organic solvent and derivatizing agent; the operation is simple, convenient and rapid for the trace analysis of beta-agonists and beta-blockers in biological fluids; it can be readily generalized for high sample throughput. So, it is hopeful that the study will facilitate the monitoring of beta-agonists and beta-blockers in the competition sports.
建立了一种采用中空纤维保护液相微萃取(HF-LPME)结合原位衍生化,随后进行气相色谱/质谱(GC/MS)分析尿液中β-激动剂和β-阻滞剂的方法。由于该方法在HF-LPME中能通过甲苯和N-甲基-N-(三甲基硅基)三氟乙酰胺(MSTFA)同时萃取和衍生目标化合物,克服了耗时且操作繁琐的缺点,同时提高了富集倍数。优化条件为:在pH 12.0和14%(w/v)NaCl的5.0 mL样品中,以925 rpm的搅拌速度,用5.0 μL混合萃取溶剂(甲苯/MSTFA = 1:1,v/v)在35℃下萃取20 min。该方法线性范围非常宽(0.25 - 400 ng mL⁻¹),对克伦特罗、美托洛尔和普萘洛尔的检测限低至0.08 - 0.10 ng mL⁻¹,富集因子高达256。该方法用于加标尿液中分析物的测定时,萃取效率高(回收率为93.79 - 109.04%)且精密度好(相对标准偏差<9.70%)。对于单次服用50 mg美托洛尔36 h后的实际人体尿液样品分析结果令人满意。所提出的方法仅需几微升有机溶剂和衍生化试剂;操作简单、方便、快速,适用于生物流体中β-激动剂和β-阻滞剂的痕量分析;可很容易地推广用于高通量样品分析。因此,有望该研究将有助于竞技体育中β-激动剂和β-阻滞剂的监测。