Cui Lili, Wang Zhipeng, Qiu Shi, Zhang Mengwei, Liu Yanping, Xu Fengjing, Song Xinhua, Gao Shouhong, Chen Wansheng
Department of Pharmacy, Second Affiliated Hospital of Naval Medical University, Shanghai 200003, China.
Research and Development Center of Chinese Medicine Resources and Biotechnology, Institute of Chinese Materia Medica, Shanghai University of Traditional Chinese Medicine, Shanghai 201203, China.
J Anal Methods Chem. 2022 Jan 5;2022:6058445. doi: 10.1155/2022/6058445. eCollection 2022.
Hydroxychloroquine (HCQ) was originally used as an antimalarial and immunomodulation drug. We developed and validated a simple and sensitive ultrahigh performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS) method for simultaneous quantitation of HCQ and its three metabolites in rat blood, and reported their pharmacokinetic parameters. The chromatographic separation and detection of analytes were achieved within 4 min on ZORBAX SB-C (3.5 m, 2.1 × 150 mm) column with gradient elution, and the flow rate was 0.25 mL/min. Simple protein precipitation was successfully applied for sample pretreatment. The HCQ displays a good linearity in the range of 2.0-5000.0 ng/mL, and the three metabolites also show good linearity ranging from 1.0 to 2500.0 ng/mL, with all correlation coefficients ( ) better than 0.98. In conclusion, this rapid, sensitive method was successfully developed, validated, and then applied to a pharmacokinetic study of HCQ in rat model in high dose. The results of the pharmacokinetic study presented an average half-life time 21.14 ± 10.31 h (mean ± SD) of HCQ, which is much shorter in human compared to that in mice. For the three metabolites, longer half-life times (approximately 100 h) were shown in rat.
羟氯喹啉(HCQ)最初用作抗疟和免疫调节药物。我们开发并验证了一种简单且灵敏的超高效液相色谱-串联质谱法(UHPLC-MS/MS),用于同时定量大鼠血液中的HCQ及其三种代谢物,并报告了它们的药代动力学参数。在ZORBAX SB-C(3.5μm,2.1×150mm)柱上通过梯度洗脱在4分钟内实现了分析物的色谱分离和检测,流速为0.25mL/min。简单的蛋白沉淀法成功应用于样品预处理。HCQ在2.0 - 5000.0ng/mL范围内显示出良好的线性,三种代谢物在1.0至2500.0ng/mL范围内也显示出良好的线性,所有相关系数( )均优于0.98。总之,这种快速、灵敏的方法成功开发、验证,并随后应用于高剂量大鼠模型中HCQ的药代动力学研究。药代动力学研究结果表明,HCQ的平均半衰期为21.14±10.31小时(平均值±标准差),与人类相比,在小鼠体内的半衰期要短得多。对于三种代谢物,在大鼠体内显示出更长的半衰期(约100小时)。