Lee Hyun-Soo, Kang Il-Mo, Lee Heon-Woo, Seo Ji-Hyung, Ryu Ju-Hee, Choi Sang-Jun, Lee Myung-Jae, Jeong Seo-Young, Cho Young-Wuk, Lee Kyung-Tae
College of Pharmacy, Kyung-Hee University, Hoegi-Dong, Dongdaemun-Ku, Seoul 130-701, Republic of Korea.
J Chromatogr B Analyt Technol Biomed Life Sci. 2008 Feb 15;863(1):158-62. doi: 10.1016/j.jchromb.2007.11.032. Epub 2007 Dec 4.
A simple and specific method using a one-step liquid-liquid extraction (LLE) with butyl acetate followed by high performance liquid chromatography (HPLC) coupled with positive ion electrospray ionization tandem mass spectrometry (ESI-MS/MS) detection was developed for the determination of etodolac in human plasma, using indomethacin as an internal standard (IS). Chromatographic separation was performed isocratically using a Capcellpak MGII C(18) column with 65% acetonitrile and 35% water containing 10mM ammonium formate (adjusted to pH 3.5 with formic acid). Acquisition was performed in multiple reaction monitoring (MRM) mode by monitoring the transitions: m/z 287.99>172.23 for etodolac and m/z 357.92>139.01 for IS. The method was validated to determine its selectivity, linearity, sensitivity, precision, accuracy, recovery and stability. The limit of quantitation (LLOQ) was 0.1microg/mL with a relative standard deviation of less than 15%. The devised method provides an accurate, precise and sensitive tool for determining etodolac levels in plasma.
建立了一种简单且特异的方法,该方法采用一步乙酸丁酯液-液萃取(LLE),随后进行高效液相色谱(HPLC)结合正离子电喷雾电离串联质谱(ESI-MS/MS)检测,以吲哚美辛作为内标(IS)来测定人血浆中的依托度酸。使用Capcellpak MGII C(18)柱,以含10mM甲酸铵(用甲酸调至pH 3.5)的65%乙腈和35%水进行等度色谱分离。通过监测跃迁进行多反应监测(MRM)模式采集:依托度酸的m/z 287.99>172.23以及内标的m/z 357.92>139.01。对该方法进行了验证,以确定其选择性、线性、灵敏度、精密度、准确度、回收率和稳定性。定量限(LLOQ)为0.1μg/mL,相对标准偏差小于15%。所设计的方法为测定血浆中依托度酸水平提供了一种准确、精密且灵敏的工具。