闫鑫, 曹玉珍, 姜小梅, 汪曣, 石玉杰. 离子液体对环孢素A口服吸收的影响J. 药学学报, 2022,57(4): 1180-1186. doi: 10.16438/j.0513-4870.2021-1668
引用本文: 闫鑫, 曹玉珍, 姜小梅, 汪曣, 石玉杰. 离子液体对环孢素A口服吸收的影响J. 药学学报, 2022,57(4): 1180-1186. doi: 10.16438/j.0513-4870.2021-1668
YAN Xin#, CAO Yu-zhen, JIANG Xiao-mei, WANG Yan, SHI Yu-jie. The effect of ionic liquid on the oral absorption of cyclosporine AJ. Acta Pharmaceutica Sinica, 2022,57(4): 1180-1186. doi: 10.16438/j.0513-4870.2021-1668
Citation: YAN Xin#, CAO Yu-zhen, JIANG Xiao-mei, WANG Yan, SHI Yu-jie. The effect of ionic liquid on the oral absorption of cyclosporine AJ. Acta Pharmaceutica Sinica, 2022,57(4): 1180-1186. doi: 10.16438/j.0513-4870.2021-1668

离子液体对环孢素A口服吸收的影响

The effect of ionic liquid on the oral absorption of cyclosporine A

  • 摘要: 研究基于胆碱和香茅酸的离子液体(ChoCA,COCA)对难溶性药物环孢素A (CsA)口服吸收的影响。由胆碱和香茅酸采用一步中和法制备COCA,对其进行质谱、核磁共振氢谱1H-NMR和红外光谱表征后,采用超声辅助法制备CsA-离子液体(CsA-COCA),并将其灌装于肠溶胶囊,液相色谱-串联质谱法(LC-MS/MS)检测大鼠分别口服CsA-COCA胶囊剂及CsA混悬剂后全血中CsA的浓度,并采用DAS 2.0软件计算药代动力学参数。动物福利和实验过程均遵循北京大学医学部动物伦理委员会的规定。研究结果表明,与口服10 mg·kg-1 CsA混悬液相比,口服相同剂量的离子液体制剂所获得的CsA的药时曲线下面积(area under the curve,AUC)提高了2.81倍,半衰期(half-life time,T1/2)延长了4.41倍,平均驻留时间(mean residence time,MRT)提高了1.77倍。本研究制备的COCA可显著促进CsA在大鼠体内的口服吸收,且能延长其半衰期。本研究可为CsA等难溶性药物的口服制剂研究提供借鉴。

     

    Abstract: To investigate the effect of ionic liquid based on choline and citronellic acid (Cho CA, COCA) on the oral absorption of poorly soluble drug cyclosporin A (CsA), COCA was synthesized using choline and citronellic acid by one-step neutralization method, and then characterized by mass spectrometry, 1H-NMR, and infrared spectrophotometry. Next, CsA-ionic liquid (CsA-COCA) was prepared by ultrasonic-assisted method and filled into enteric-coated capsules. After oral administration of CsA-COCA capsules or CsA suspension preparation in rats, CsA concentration in whole blood was assayed using liquid chromatography-tandem mass spectrometry (LC-MS/MS) method, and the pharmacokinetic parameters were calculated by DAS 2.0 software. All animal care and experiments followed the approval of Institutional Animal Care and Use Committee at Peking University Health Science Center. The results indicated that compared with oral administration of 10 mg·kg-1CsA suspension, the area under the curve (AUC), half-life time (T1/2), and mean residence time (MRT) of CsA obtained by oral administration the same dose of CsA-COCA increased by 2.81, 4.41, and 1.77 times, respectively. The COCA prepared in this study can significantly promote the oral absorption of CsA in rats, and prolong the half-life. This study can provide reference for the study of oral formulation of insoluble drugs such as CsA.

     

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