Xia Jing, Kotani Akira, Hakamata Hideki, Kusu Fumiyo
Department of Traditional Chinese Medicine, Shanghai Institute for Drug Control, No 615 Liuzhou Road, Shanghai 200233, China.
J Pharm Biomed Anal. 2006 Jun 16;41(4):1401-5. doi: 10.1016/j.jpba.2006.02.030. Epub 2006 Mar 31.
Determination of hesperidin contents in Pericarpium Citri Reticulatae was performed by a simple extraction with methanol and semi-micro high-performance liquid chromatography with electrochemical detection (muHPLC-ECD). Chromatography was performed using a microbore octadecylsilica (ODS) column, methanol-water-phosphoric acid (40:60:0.5, v/v/v), as a mobile phase and applied potential at +0.9 V versus Ag/AgCl. Peak heights were found linearly related to the concentrations of hesperidin injected 9.16 ng/ml to 3.06 microg/ml (r>0.999). The detection limit (S/N=3) was 3.06 ng/ml (15.3 pg). Hesperidin of 305 ng/ml was detected with a relative standard deviation (R.S.D.) of 0.79% (n=5). Hesperidin in Pericarpium Citri Reticulatae was extracted with methanol, diluted with the mobile phase, and injected into the muHPLC-ECD for determination. The hesperidin content of Pericarpium Citri Reticulatae from four different districts in China were determined with R.S.D. of 3.59%, 2.29%, 2.36%, and 2.32% (n=5), respectively. Recoveries of hesperidin from the four Pericarpium Citri Reticulatae sources were 100.3%, 99.83%, 100.7%, and 100.6%, respectively. This method is useful for the determination of hesperidin in Pericarpium Citri Reticulatae, and especially so for instances when samples are sparse.
采用甲醇简单提取法和半微高效液相色谱-电化学检测法(μHPLC-ECD)测定陈皮中橙皮苷的含量。色谱分析使用微径十八烷基硅胶(ODS)柱,以甲醇-水-磷酸(40:60:0.5,v/v/v)作为流动相,相对于Ag/AgCl施加+0.9 V的电位。发现峰高与注入的橙皮苷浓度在9.16 ng/ml至3.06 μg/ml之间呈线性关系(r>0.999)。检测限(S/N = 3)为3.06 ng/ml(15.3 pg)。检测到305 ng/ml的橙皮苷,相对标准偏差(R.S.D.)为0.79%(n = 5)。陈皮中的橙皮苷用甲醇提取,用流动相稀释,然后注入μHPLC-ECD进行测定。测定了来自中国四个不同地区的陈皮中橙皮苷的含量,R.S.D.分别为3.59%、2.29%、2.36%和2.32%(n = 5)。从四种陈皮来源中回收橙皮苷的回收率分别为100.3%、99.83%、100.7%和100.6%。该方法可用于测定陈皮中的橙皮苷,特别是在样品稀少的情况下。