Ghosheh O A, Houdi A A, Crooks P A
Department of Pharmaceutical Sciences, College of Pharmacy, University of Kentucky, Lexington 40536, USA.
J Pharm Biomed Anal. 1999 Apr;19(5):757-62. doi: 10.1016/s0731-7085(98)00300-8.
An HPLC method for quantifying the putative pharmacologically active constituents: thymoquinone (TQ), dithymoquinone (DTQ), thymohydroquinone (THQ), and thymol (THY), in the oil of Nigella sativa seed is described. Extraction of the constituents from the oil was carried out using C18 PrepSep mini columns followed by quantification of the recovered constituents by HPLC on a reversed-phase muBondapak C18 analytical column, using an isocratic mobile phase of water:methanol:2-propanol (50:45:5% v/v) at a flow rate of 2 ml min(-1). UV detection was at 254 nm for TQ, DTQ, and THY, and at 294 nm for THQ. The above four compounds were separated with good resolution, reproducibility, and sensitivity under these conditions. This analytical method was used to quantify the above four constituents in a commercial sample of N. sativa seed oil, and provides a good quality control methodology for the pharmacologically active components in this widely used natural remedy.
百里醌(TQ)、二百里醌(DTQ)、百里氢醌(THQ)和百里酚(THY)的高效液相色谱法。使用C18 PrepSep微型柱从精油中提取成分,然后在反相μBondapak C18分析柱上通过高效液相色谱法对回收的成分进行定量,使用水:甲醇:2-丙醇(50:45:5% v/v)的等度流动相,流速为2 ml min⁻¹。TQ、DTQ和THY的紫外检测波长为254 nm,THQ的紫外检测波长为294 nm。在这些条件下,上述四种化合物得到了良好的分离,具有良好的分辨率、重现性和灵敏度。该分析方法用于定量市售黑种草籽精油样品中的上述四种成分,并为这种广泛使用的天然药物中的药理活性成分提供了一种良好的质量控制方法。