College of Pharmacy, Nanjing University of Chinese Medicine, Nanjing 210046, PR China; Jiangsu Engineering Research Center for Efficient Delivery System of TCM, PR China; Nanjing Engineering Research Center for Industrialization of Chinese Medicine Pellets, PR China.
First Medicine College, Nanjing University of Chinese Medicine, Nanjing 210046, PR China.
J Chromatogr B Analyt Technol Biomed Life Sci. 2014 Feb 15;949-950:7-15. doi: 10.1016/j.jchromb.2013.12.035. Epub 2014 Jan 7.
The current study aims to investigate the pharmacokinetic study of eight caffeic acid derivatives (forsythoside A, isoforsythoside, forsythoside B, neochlorogenic acid, chlorogenic acid, cryptochlorogenic acid, 3,5-dicaffeoylquinic acid and 3,4-dicaffeoylquinic acid) following oral administration of Flos Lonicerae-Fructus Forsythiae herb combination in rats. A rapid and sensitive ultra performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method was developed to determine the eight caffeic acid derivatives simultaneously in rat plasma. After mixing with the internal standard (IS) tinidazole, plasma samples were pretreated by liquid-liquid extraction with n-butyl alcohol/ethyl acetate (7:3, v/v). The separation was performed on an Acquity UPLC HSS T3 C18 column (100mm×2.1mm, 1.8μm) at a flow rate of 0.4mLmin(-1), and acetonitrile/methanol (4:1, v/v)-0.4% formic acid was used as mobile phase. The detection was performed on a triple quadrupole tandem mass spectrometer by multiple reaction monitoring (MRM) via electrospray ionization (ESI) source with positive and negative ionization modes. All calibration curves had good linearity (r>0.991) over the concentration ranges of 1.097-2246ngmL(-1) for neochlorogenic acid, 6.535-6692ngmL(-1) for chlorogenic acid, 2.103-2153ngmL(-1) for cryptochlorogenic acid, 0.5058-129.5ngmL(-1) for 3,5-dicaffeoylquinic acid, 0.3205-82.05ngmL(-1) for 3,4-dicaffeoylquinic acid, 1.002-512.8ngmL(-1) for isoforsythoside, 0.4795-982.1ngmL(-1) for forsythoside A and 0.7587-776.9ngmL(-1) for forsythoside B, respectively. The intra- and inter-batch precisions were all within 15% and the accuracy (relative error, RE%) all ranged from 85.68% to 114.7%. It was shown from pharmacokinetic parameters that the rank order of AUC0-t, Cmax and T1/2k for phenolic acids was chlorogenic acid>neochlorogenic acid≥cryptochlorogenic acid>3,4-dicaffeoylquinic acid≥3,5-dicaffeoylquinic acid (most of them had significant differences), which corresponded to their administration dosages to rats, but that of MRT0-t and T1/2z were opposite. Besides, the AUC0-t, Cmax, MRT and T1/2z except T1/2k of isoforsythoside and forsythoside B had no significant difference, compared to that of forsythoside A though their administration dosages were significantly lower than that of forsythoside A. All results showed that the method was applied to the pharmacokinetic study of the eight caffeic acid derivatives in rat plasma successfully after oral administration of Flos Lonicerae-Fructus Forsythiae herb combination, and there were significant differences of caffeic acid derivatives even isomers in the pharmacokinetic parameters.
目前的研究旨在调查口服金银花-连翘药草组合后八种咖啡酸衍生物(连翘酯苷 A、异连翘酯苷、连翘酯苷 B、新绿原酸、绿原酸、隐绿原酸、3,5-二咖啡酰奎宁酸和 3,4-二咖啡酰奎宁酸)的药代动力学研究。建立了一种快速灵敏的超高效液相色谱-串联质谱(UPLC-MS/MS)法,同时测定大鼠血浆中的八种咖啡酸衍生物。与内标(替硝唑)混合后,用正己烷/乙酸乙酯(7:3,v/v)进行液-液萃取预处理。分离在 Acquity UPLC HSS T3 C18 柱(100mm×2.1mm,1.8μm)上进行,流速为 0.4mLmin(-1),流动相为乙腈/甲醇(4:1,v/v)-0.4%甲酸。通过电喷雾电离(ESI)源,采用正、负离子模式进行多反应监测(MRM)检测。新绿原酸、绿原酸、隐绿原酸、3,5-二咖啡酰奎宁酸、3,4-二咖啡酰奎宁酸、异连翘酯苷、连翘酯苷 A 和连翘酯苷 B 的浓度范围分别为 1.097-2246ngmL(-1)、6.535-6692ngmL(-1)、2.103-2153ngmL(-1)、0.5058-129.5ngmL(-1)、0.3205-82.05ngmL(-1)、1.002-512.8ngmL(-1)、0.4795-982.1ngmL(-1)和 0.7587-776.9ngmL(-1)时,所有校准曲线均具有良好的线性(r>0.991)。内、批间精密度均在 15%以内,准确度(相对误差,RE%)均在 85.68%-114.7%之间。从药代动力学参数可以看出,酚酸类物质的 AUC0-t、Cmax 和 T1/2k 的排序为绿原酸>新绿原酸≥隐绿原酸>3,4-二咖啡酰奎宁酸>3,5-二咖啡酰奎宁酸(其中大部分差异显著),这与它们在大鼠中的给药剂量相对应,但 MRT0-t 和 T1/2z 的情况则相反。此外,异连翘酯苷和连翘酯苷 B 的 AUC0-t、Cmax、MRT 和 T1/2z 除 T1/2k 外,与连翘酯苷 A 相比均无显著差异,尽管它们的给药剂量明显低于连翘酯苷 A。所有结果表明,该方法成功应用于金银花-连翘药草组合口服后大鼠血浆中八种咖啡酸衍生物的药代动力学研究,即使是咖啡酸衍生物的同分异构体,其药代动力学参数也存在显著差异。