Wu Yu-Tse, Lin Lie-Chwen, Sung Jung-Sung, Tsai Tung-Hu
Institute of Traditional Medicine, National Yang-Ming University, Taipei 112, Taiwan.
J Chromatogr B Analyt Technol Biomed Life Sci. 2006 Nov 21;844(1):89-95. doi: 10.1016/j.jchromb.2006.07.011. Epub 2006 Aug 4.
A sensitive LC-MS/MS method with a simple solid-phase extraction for the determination of acteoside in rat plasma and tissue homogenates was established for the investigation of bioavailability and brain distribution in freely-moving rats. Acteoside in Cistanche deserticola and Boschniakia rossica was also determined. Acteoside and internal standard were separated on a RP-select B column (125mmx4.6mm i.d., particle size 5microm). The mobile phase consisted of 35% methanol and 65% acetic acid-water (1:100, v/v) at a flow-rate of 1mL/min. Acteoside and the internal standard were monitored using the multiple-reaction monitoring (MRM) mode at m/z transitions of 623-->161 and 609-->301, respectively. The acteoside content was 38.4+/-2.4mg/kg (n=3) for B. rossica, which is obviously lower than 21134.2+/-805.5mg/kg (n=3) of C. deserticola. The protein binding in rat plasma was 75.5+/-1.8%. The brain distribution result indicated that acteoside was evenly distributed in brain tissues (brain stem, cerebellum, the rest of the brain, cortex, hippocampus and striatum) which was about 0.45-0.68% of that in plasma (4.5+/-0.5microg/mL) after 15min of acteoside administration (10mg/kg, i.v.). After acteoside was given (3mg/kg, i.v.; 100mg/kg, p.o.), the oral bioavailability (AUC(p.o.)/dose(p.o.))/(AUC(i.v.)/dose(i.v.)) was only 0.12%.
建立了一种采用简单固相萃取的灵敏液相色谱-串联质谱法,用于测定大鼠血浆和组织匀浆中的松果菊苷,以研究其在自由活动大鼠体内的生物利用度和脑分布情况。同时还测定了肉苁蓉和草苁蓉中的松果菊苷。松果菊苷和内标物在RP-select B柱(125mm×4.6mm内径,粒径5μm)上分离。流动相由35%甲醇和65%醋酸-水(1:100,v/v)组成,流速为1mL/min。采用多反应监测(MRM)模式分别在m/z 623→161和609→301处监测松果菊苷和内标物。草苁蓉中松果菊苷含量为38.4±2.4mg/kg(n = 3),明显低于肉苁蓉的21134.2±805.5mg/kg(n = 3)。大鼠血浆中的蛋白结合率为75.5±1.8%。脑分布结果表明,静脉注射松果菊苷(10mg/kg)15分钟后,松果菊苷在脑组织(脑干、小脑、脑其余部分、皮质、海马和纹状体)中均匀分布,约为血浆中含量(4.5±0.5μg/mL)的0.45 - 0.68%。给予松果菊苷(静脉注射3mg/kg;口服100mg/kg)后,口服生物利用度(AUC(口服)/剂量(口服))/(AUC(静脉注射)/剂量(静脉注射))仅为0.12%。