Medvedovici Andrei, Udrescu Stefan, David Victor
University of Bucharest, Faculty of Chemistry, Department of Analytical Chemistry, 90 Panduri Av., Bucharest, Romania.
Biomed Chromatogr. 2013 Jan;27(1):48-57. doi: 10.1002/bmc.2747. Epub 2012 Apr 18.
Limonene, considered a green solvent, was successfully used to extract simvastatin, lovastatin, and their hydroxy-acid metabolites from human plasma samples. The extraction process was followed by the direct injection of a large volume aliquot (100 μL) from the limonene layer into a Zorbax SB-C(18) Rapid Resolution chromatographic column (50 mm length × 4.6 mm i.d. × 1.8 µm d.p.), operated under gradient elution reversed-phase separation mechanism. Tandem mass spectrometry operated under the multiple reaction monitoring mode was used for detection, providing low quantitation limits in the 0.25-0.5 ng/mL concentration interval. This method was validated and used for quantitation of simvastatin and its hydroxy acid metabolite in incurred plasma samples obtained from two volunteers participating in a bioequivalence study, using lovastatin and its hydroxy analog as internal standards. The results were statistically compared with those produced by means of an alternative RPLC-tandem MS using protein precipitation with acetonitrile. The quality attributes of the two methods are comparatively discussed. The agreement between the quality characteristics of the two methods and the experimental results obtained on real samples may be considered as a consistent basis for the simultaneous use of limonene as extraction medium and injection diluent for hydrophobic compounds in bioanalytical approaches.
柠檬烯被认为是一种绿色溶剂,已成功用于从人血浆样本中提取辛伐他汀、洛伐他汀及其羟基酸代谢物。提取过程之后,将来自柠檬烯层的大量等分试样(100 μL)直接注入Zorbax SB-C(18)快速分离色谱柱(柱长50 mm×内径4.6 mm×粒径1.8 µm),该色谱柱在梯度洗脱反相分离机制下运行。采用多反应监测模式的串联质谱进行检测,在0.25 - 0.5 ng/mL浓度区间提供低定量限。该方法经过验证,并用于对参与生物等效性研究的两名志愿者的实际血浆样本中的辛伐他汀及其羟基酸代谢物进行定量,使用洛伐他汀及其羟基类似物作为内标。将结果与通过使用乙腈进行蛋白质沉淀的另一种反相液相色谱 - 串联质谱法得到的结果进行统计学比较。对两种方法的质量属性进行了比较讨论。两种方法的质量特性与在实际样品上获得的实验结果之间的一致性,可被视为在生物分析方法中同时使用柠檬烯作为疏水化合物的提取介质和进样稀释剂的一致依据。