采用液相色谱-串联质谱法测定总霉酚酸、游离霉酚酸和唾液霉酚酸:在健康志愿者和肾移植患者药代动力学研究中的应用
Determination of total, free and saliva mycophenolic acid with a LC-MS/MS method: application to pharmacokinetic study in healthy volunteers and renal transplant patients.
作者信息
Shen Bing, Li Shuijun, Zhang Yuan, Yuan Xuelu, Fan Yu, Liu Zhihong, Hu Qiang, Yu Chen
机构信息
Department of Renal Transplantation and Urology, Shanghai First People's Hospital, Institute of Organ Transplantation, Shanghai Jiaotong University, Shanghai, 200080, China.
出版信息
J Pharm Biomed Anal. 2009 Oct 15;50(3):515-21. doi: 10.1016/j.jpba.2009.05.030. Epub 2009 Jun 6.
Mycophenolic acid (MPA) is the active moiety of mycophenoate mofetil (MMF), an ester prodrug widely used as an immunosuppressant. Therapeutic drug monitoring (TDM) of MPA is becoming mandatory for transplant patients received MMF therapy in the routine clinical practice because of large individual variability, dose-related toxicity and the risk of acute rejection. In this study, a rapid, sensitive and selective LC-MS/MS method was developed and validated for the quantitative analysis of total and free MPA in plasma and in saliva that uses one identical liquid chromatographic and mass spectrometric condition. Following protein precipitation for total and saliva MPA, and ultrafiltration for free MPA, chromatographic separation was performed on an Allure PFP Propyl analytical column (100 x 2.1 mm, 5 microm, RESTEK Co., Bellefonte, PA, USA) with 0.1% formic acid in acetonitrile and 0.1% formic acid in water (45:55, v/v) as the mobile phases. The compounds were quantified by positive electrospray ionization tandem mass spectrometry. Selectivity, linearity, accuracy, precision, recovery, matrix effect, and saliva stability were evaluated during method validation. The validated method was applied to a pharmacokinetic study of MPA after an oral administration of a single 1000 mg of MMF to eight healthy male volunteers and 750 mg bid of MMF to nine renal transplant patients.
霉酚酸(MPA)是霉酚酸酯(MMF)的活性部分,MMF是一种广泛用作免疫抑制剂的酯前药。由于个体差异大、剂量相关毒性以及急性排斥反应风险,在常规临床实践中,接受MMF治疗的移植患者进行MPA治疗药物监测(TDM)已成为强制性要求。在本研究中,开发并验证了一种快速、灵敏且选择性的LC-MS/MS方法,用于定量分析血浆和唾液中的总MPA和游离MPA,该方法采用相同的液相色谱和质谱条件。对于总MPA和唾液MPA,采用蛋白沉淀法;对于游离MPA,采用超滤法。在Allure PFP丙基分析柱(100×2.1 mm,5μm,美国宾夕法尼亚州贝勒方特的RESTEK公司)上进行色谱分离,流动相为乙腈中的0.1%甲酸和水中的0.1%甲酸(45:55,v/v)。通过正电喷雾电离串联质谱对化合物进行定量。在方法验证过程中评估了选择性、线性、准确性、精密度、回收率、基质效应和唾液稳定性。经验证的方法应用于8名健康男性志愿者单次口服1000 mg MMF以及9名肾移植患者每日两次口服750 mg MMF后MPA的药代动力学研究。