Nirogi Ramakrishna, Kandikere Vishwottam, Mudigonda Koteshwara, Komarneni Prashanth
Biopharmaceutical Research, Suven Life Sciences Ltd, Serene Chambers, Road 5, Avenue 7, Banjara Hills, Hyderabad 500034, India.
Biomed Chromatogr. 2008 Sep;22(9):992-1000. doi: 10.1002/bmc.1018.
A sensitive high-performance liquid chromatography-positive ion electrospray tandem mass spectrometry method was developed and validated for the quantification of clonidine in human plasma. Following liquid-liquid extraction, the analytes were separated using an isocratic mobile phase on a reverse-phase column and analyzed by MS/MS in the multiple reaction monitoring mode using the respective M + H ions, m/z 230 to 44 for clonidine and m/z 254 to 44 for the internal standard. The assay exhibited a linear dynamic range of 10-2000 pg/mL for clonidine in human plasma. The lower limit of quantification was 10 pg/mL with a relative standard deviation of less than 6.8%. Acceptable precision and accuracy were obtained for concentrations over the standard curve range. A run time of 2.5 min for each sample made it possible to analyze more than 250 human plasma samples per day. The validated method was successfully used to analyze human plasma samples for application in pharmacokinetic studies.
建立了一种灵敏的高效液相色谱 - 正离子电喷雾串联质谱法,并对其进行了验证,用于定量测定人血浆中的可乐定。液 - 液萃取后,使用等度流动相在反相柱上分离分析物,并在多反应监测模式下通过MS/MS使用各自的M + H离子进行分析,可乐定的m/z为230至44,内标的m/z为254至44。该测定法在人血浆中可乐定的线性动态范围为10 - 2000 pg/mL。定量下限为10 pg/mL,相对标准偏差小于6.8%。在标准曲线范围内的浓度获得了可接受的精密度和准确度。每个样品的运行时间为2.5分钟,使得每天能够分析超过250份人血浆样品。该验证方法成功用于分析人血浆样品,以应用于药代动力学研究。