He Huan, Li Li, Zhao Libo, Sun Ning, Zhang Meng, Cheng Ying, Yu Lu, Ma Lin, Wang Xiaoling
Clinical Research Center, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health Beijing 100045 China
Department of Dermatology, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health Beijing 100045 China
RSC Adv. 2018 Nov 7;8(65):37286-37294. doi: 10.1039/c8ra06252h. eCollection 2018 Nov 1.
Propranolol is now a preferred treatment for infantile hemangioma. However, there are no published papers on the metabolism and concentrations of propranolol in the plasma of infants with hemangioma. In the present study, a sensitive, simple and reliable method was developed and validated for the simultaneous quantification of propranolol and its metabolites 4-hydroxypropranolol (M1) and -desisopropylpropranolol (M2) in infants' plasma for the first time by using liquid chromatography-tandem mass spectrometry (LC-MS/MS). A volume of 100 μL plasma was prepared by one-step protein precipitation with acetonitrile (300 μL), followed by its separation on an Hypersil GOLD C column maintained at 40 °C with gradient mobile phase consisting of 0.1% formic acid aqueous solution and acetonitrile at a flow rate of 0.3 mL min. The quantification was performed multiple reaction monitoring (MRM) by a triple quadrupole mass spectrometer under positive electrospray ionization (ESI) mode. Bisoprolol was chosen as the internal standard. The method was validated to demonstrate its selectivity, linearity, accuracy, precision, recovery, matrix effect and stability. The matrix-matched calibration curves for propranolol ranging from 1 to 500 ng mL, for M1 ranging from 0.2 to 100 ng mL and for M2 ranging from 0.2 to 100 ng mL were all linear, with correlation coefficients calculated using weighted (1/ ) least square linear regression analysis. The lower limits of quantification (LLOQs) were 1 ng mL, 0.2 ng mL and 0.2 ng mL for propranolol, M1 and M2, respectively. The intra-day and inter-day precisions were less than 7.1% and relative errors were all less than 9.8%. This validated method was successfully applied to quantify the concentrations of propranolol and its metabolites 4-hydroxypropranolol (M1) and -desisopropylpropranolol (M2) in the plasma of infants with hemangioma after oral administration of different doses of propranolol for the first time.
普萘洛尔现在是婴儿血管瘤的首选治疗药物。然而,关于普萘洛尔在血管瘤婴儿血浆中的代谢和浓度,尚无已发表的论文。在本研究中,首次开发并验证了一种灵敏、简单且可靠的方法,用于通过液相色谱 - 串联质谱法(LC-MS/MS)同时定量婴儿血浆中的普萘洛尔及其代谢物4-羟基普萘洛尔(M1)和去异丙基普萘洛尔(M2)。取100μL血浆,用乙腈(300μL)一步法进行蛋白沉淀,然后在Hypersil GOLD C柱上分离,该柱保持在40℃,流动相为梯度洗脱,由0.1%甲酸水溶液和乙腈组成,流速为0.3 mL/min。通过三重四极杆质谱仪在正电喷雾电离(ESI)模式下采用多反应监测(MRM)进行定量。选择比索洛尔作为内标。该方法经过验证,证明了其选择性、线性、准确性、精密度、回收率、基质效应和稳定性。普萘洛尔的基质匹配校准曲线范围为1至500 ng/mL,M1为0.2至100 ng/mL,M2为0.2至100 ng/mL,均呈线性,相关系数采用加权(1/x²)最小二乘线性回归分析计算。普萘洛尔、M1和M2的定量下限(LLOQ)分别为1 ng/mL、0.2 ng/mL和0.2 ng/mL。日内和日间精密度均小于7.1%,相对误差均小于9.8%。这种经过验证的方法首次成功应用于定量口服不同剂量普萘洛尔后血管瘤婴儿血浆中普萘洛尔及其代谢物4-羟基普萘洛尔(M1)和去异丙基普萘洛尔(M2)的浓度。