Zhu Hao-Jie, Wang Jun-Sheng, Patrick Kennerly S, Donovan Jennifer L, DeVane C Lindsay, Markowitz John S
Laboratory of Drug Disposition and Pharmacogenetics, Medical University of South Carolina, USA.
J Chromatogr B Analyt Technol Biomed Life Sci. 2007 Oct 15;858(1-2):91-5. doi: 10.1016/j.jchromb.2007.08.014. Epub 2007 Aug 19.
A number of analytical methods have been established to quantify methylphenidate (MPH). However, to date no HPLC methods are applicable to human pharmacokinetic studies without the use of mass spectrometry (MS) detection. We developed a sensitive and reliable HPLC-fluorescence method for the determination of MPH in human plasma using 4-(4,5-diphenyl-1H-imidazol-2-yl) benzoyl chloride (DIB-Cl) as the derivatizing agent. An established GC-MS method was adopted in this study as a comparator assay. MPH was derivatized using DIB-Cl, and separated isocratically on a C18 column using a HPLC system with fluorescence detection (lambda(ex)=330 nm, lambda(em)=460 nm). The lower limit of quantification was found to be 1 ng/mL. A linear calibration curve was obtained over the concentrations ranging from 1 ng/mL to 80 ng/mL (r=0.998). The relative standard deviations of intra-day and inter-day variations were <or=9.10% and <or=7.58%, respectively. The accuracy ranged between 92.59% and 103.06%. The method was successfully applied to the pharmacokinetic study of a subject who received a single oral dose (0.3 mg/kg) of immediate-release MPH and yielded consistent results with that of the GC-MS method. This method is the first HPLC assay with non-MS detection providing sufficient reliability and sensitivity for both pre-clinical and clinical studies of MPH.
已经建立了多种分析方法来定量测定哌甲酯(MPH)。然而,迄今为止,没有一种高效液相色谱(HPLC)方法在不使用质谱(MS)检测的情况下适用于人体药代动力学研究。我们开发了一种灵敏可靠的HPLC荧光法,以4-(4,5-二苯基-1H-咪唑-2-基)苯甲酰氯(DIB-Cl)作为衍生化试剂来测定人血浆中的MPH。本研究采用已建立的气相色谱-质谱(GC-MS)方法作为对照测定法。MPH用DIB-Cl进行衍生化,然后使用配备荧光检测(激发波长λ(ex)=330 nm,发射波长λ(em)=460 nm)的HPLC系统在C18柱上进行等度分离。定量下限为1 ng/mL。在1 ng/mL至80 ng/mL的浓度范围内获得了线性校准曲线(r=0.998)。日内和日间变异的相对标准偏差分别≤9.10%和≤7.58%。准确度在92.59%至103.06%之间。该方法成功应用于一名单次口服速释MPH(0.3 mg/kg)受试者的药代动力学研究,并与GC-MS方法得出了一致的结果。该方法是首个不使用MS检测的HPLC测定法,为MPH的临床前和临床研究提供了足够的可靠性和灵敏度。