Guo Yunzhen, Yu Li, Ma Zheng, Guo Xingjie
School of Pharmacy, Shenyang Pharmaceutical University, Shenyang 110016, China.
Se Pu. 2007 Mar;25(2):211-3.
The concentration of serotonin (5-HT) in rat brain microdialysate before and after i. p. administration of fluoxetine hydrochloride was determined through precolumn derivatization by reversed-phase high performance liquid chromatography (RP-HPLC). A baseline separation of serotonin was achieved on a Hypersil C18 column (250 mm x 2. 0 mm, 5 microm) with acetonitrile-20 mmol/L sodium acetic solution (pH 5. 0) (45: 55, v/v) containing 20 mmol/L of sodium octanesulfonate as the mobile phase. Fluorescence detection with the excitation wavelength at 330 nm and emission wavelength at 455 nm was used for serotonin. There was good linear relationship between the peak area and concentration in the range of 0. 25 - 5. 0 nmol/L( r =0. 999 1). The limit of quantitation was 0. 25 nmol/L. The method is simple, accurate and can be applied to the determination of serotonin in biological specimen.
采用反相高效液相色谱(RP-HPLC)柱前衍生法测定大鼠脑微透析液中腹腔注射盐酸氟西汀前后血清素(5-HT)的浓度。在Hypersil C18柱(250 mm×2.0 mm,5μm)上,以含20 mmol/L辛烷磺酸钠的乙腈-20 mmol/L乙酸钠溶液(pH 5.0)(45:55,v/v)为流动相,实现了血清素的基线分离。血清素采用荧光检测,激发波长为330 nm,发射波长为455 nm。在0.25 - 5.0 nmol/L范围内,峰面积与浓度呈良好的线性关系(r = 0.999 1)。定量限为0.25 nmol/L。该方法简便、准确,可用于生物样品中血清素的测定。