Department of Chemistry, National University of Singapore, 3 Science Drive 3, Singapore 117543, Singapore.
Anal Chim Acta. 2011 Feb 14;687(1):56-60. doi: 10.1016/j.aca.2010.12.007. Epub 2010 Dec 11.
A cost effective and environmentally friendly extraction technique using porous membrane protected micro-solid phase extraction (μ-SPE) is described for the extraction of estrogens in cyst fluid samples obtained from cancer patients. A sorbent (ethylsilane (C2) modified silica) (20 mg) was packed in a porous polypropylene envelope (2 cm×1.5 cm) whose edges were heat sealed to secure the contents. The μ-SPE device was conditioned with acetone and placed in a stirred (1:5) diluted cyst fluid sample solution (10 mL) to extract estrogens for 60 min. After extraction, the analytes were desorbed and simultaneously derivatized with a 5:1 mixture of acetone and N,O-bis(trimethylsilyl)-trifluoroacetamide. The extract (2 μL) was analyzed by gas chromatography-mass spectrometry. Various extraction, desorption and derivatization conditions were optimized for μ-SPE. With this simple technique, low limits of detection of between 9 and 22 ng L(-1) and linear range from the detection limits up to 50 μg L(-1) were achieved. The optimized method was used to extract estrogens from cyst fluid samples obtained from patients with malignant and benign ovarian tumors.
一种使用多孔膜保护的微固相萃取(μ-SPE)的经济有效且环保的提取技术,用于从癌症患者的囊液样本中提取雌激素。将(乙基硅烷(C2)改性硅胶)(20mg)填充到多孔聚丙烯信封(2cm×1.5cm)中,边缘热封以固定内容物。用丙酮对μ-SPE 装置进行预处理,然后将其放入搅拌(1:5)稀释的囊液样品溶液(10mL)中,以提取雌激素 60 分钟。提取后,用丙酮和 N,O-双(三甲基硅基)-三氟乙酰胺的 5:1 混合物将分析物解吸并同时衍生化。用气相色谱-质谱法分析提取物(2μL)。对 μ-SPE 的各种提取、解吸和衍生化条件进行了优化。通过这种简单的技术,实现了 9 至 22ng L(-1)之间的低检测限和从检测限到 50μg L(-1)的线性范围。优化后的方法用于从患有恶性和良性卵巢肿瘤的患者的囊液样本中提取雌激素。