Pilli Nageswara Rao, Inamadugu Jaswanth Kumar, Kondreddy Neeraja, Karra Vijaya Kumari, Damaramadugu Rajasekhar, Rao J V L N Seshagiri
University College of Pharmaceutical Sciences, Jawaharlal Nehru Technological University, Kukatpally, Hyderabad-500 085, India.
Biomed Chromatogr. 2011 Aug;25(8):943-51. doi: 10.1002/bmc.1552. Epub 2010 Dec 10.
A rapid and sensitive liquid chromatography-tandem mass spectrometric (LC-MS/MS) assay method has been developed and fully validated for simultaneous quantification of donepezil and its active metabolite, 6-o-desmethyl donepezil in human plasma. Analytes and the internal standard were extracted from human plasma by liquid-liquid extraction technique using a 30:70 v/v mixture of ethyl acetate and n-hexane. The reconstituted samples were chromatographed on a C(18) column by using a 70:30 v/v mixture of acetonitrile and ammonium formate (5 mm, pH 5.0) as the mobile phase at a flow rate of 0.6 mL/min. The calibration curve obtained was linear (r ≥ 0.99) over the concentration range of 0.09-24.2 ng/mL for donepezil and 0.03-8.13 ng/mL for 6-o-desmethyl donepezil. The results of the intra-day and inter-day precision and accuracy studies were well within the acceptable limits. The proposed method was successfully applied for the estimation of the drug in real time plasma samples for pharmacokinetic studies.
已开发并完全验证了一种快速灵敏的液相色谱-串联质谱(LC-MS/MS)测定方法,用于同时定量测定人血浆中多奈哌齐及其活性代谢物6-氧去甲基多奈哌齐。采用乙酸乙酯和正己烷体积比为30:70的混合液,通过液-液萃取技术从人血浆中提取分析物和内标。重构后的样品在C(18)柱上进行色谱分析,以乙腈和甲酸铵(5 mM,pH 5.0)体积比为70:30的混合液作为流动相,流速为0.6 mL/min。所获得的校准曲线在多奈哌齐浓度范围为0.09 - 24.2 ng/mL、6-氧去甲基多奈哌齐浓度范围为0.03 - 8.13 ng/mL内呈线性(r≥0.99)。日内和日间精密度及准确度研究结果均在可接受范围内。所提出的方法成功应用于药代动力学研究的实际血浆样品中药物的测定。