Klejdus Borivoj, Mikelová Radka, Petrlová Jitka, Potesil David, Adam Vojtech, Stiborová Marie, Hodek Petr, Vacek Jan, Kizek René, Kubán Vlastimil
Department of Chemistry and Biochemistry, Mendel University of Agriculture and Forestry, Zemedelská 1, CZ-613 00 Brno, Czech Republic.
J Agric Food Chem. 2005 Jul 27;53(15):5848-52. doi: 10.1021/jf0502754.
An ultrafast HPLC/UV-vis DAD method working at 254 nm was applied for the determination of isoflavone aglycons and glycosides (genistin, genistein, daidzein, daidzin, glycitin, glycitein, ononin, formononetin, sissotrin, and biochanin A) in roots, stems, leaves, and soy pods of soy plants and in soybeans of five varieties (Korada, Quito, Rita, OAC Erin, and OAC Vison). An Atlantis dC18 ultrafast RP chromatographic column (20 mm x 2.1 mm, 3 microm particle size) was applied for separation of the isoflavone aglycons and glycosides. A flow rate of the mobile phase (0.1% (v/v) acetic acid, pH 3.75-solvent A and methanol-solvent B) was 0.35 mL min(-1), and the column temperature was 36 degrees C. A linear gradient profile from 13 up to 22% B (v/v) from zero to 2.5 min, up to 30% B to 3.21 min, up to 35% B to 4 min, up to 40% B to 4.5 min, up to 50% B to 5.14 min, and followed by negative gradient up to 13% B to 7.71 min was used. The absolute limits of detection per sample injection (5 microL) were the highest for biochanin A (166.2 fmol) and the lowest for genistin (17.0 fmol), respectively. An accelerated solvent extraction (ASE) in combination with sonication was applied for isolation of biologically active compounds. A solid-phase extraction procedure was used to purify the extracts in the case of analysis of soy plants parts. The recoveries of 96-106% were obtained for the different concentrations of the isoflavone aglycons and glycosides and the different matrixes (overall RSDs 2-9%). The highest isoflavone concentrations were found in roots (12.5 microg g(-1) dry weight), while the amounts were about 3-1100 microg g(-1) fresh weight in different varieties of soybeans.
采用一种在254 nm波长下工作的超快速高效液相色谱/紫外-可见二极管阵列检测(HPLC/UV-vis DAD)方法,测定大豆植株的根、茎、叶、豆荚以及五个品种(Korada、Quito、Rita、OAC Erin和OAC Vison)大豆中的异黄酮苷元和糖苷(染料木苷、染料木素、大豆苷元、大豆苷、甘草苷、甘草素、芒柄花苷、芒柄花素、刺芒柄花苷和鹰嘴豆芽素A)。使用Atlantis dC18超快速反相色谱柱(20 mm×2.1 mm,粒径3μm)分离异黄酮苷元和糖苷。流动相(0.1%(v/v)乙酸,pH 3.75 - 溶剂A和甲醇 - 溶剂B)流速为0.35 mL min⁻¹,柱温为36℃。采用线性梯度洗脱,0至2.5 min时B(v/v)从13%升至22%,3.21 min时升至30%,4 min时升至35%,4.5 min时升至40%,5.14 min时升至50%,随后进行负梯度洗脱至7.71 min时降至13%。每次进样(5μL)的绝对检测限,鹰嘴豆芽素A最高(166.2 fmol),染料木苷最低(17.0 fmol)。采用加速溶剂萃取(ASE)结合超声处理来分离生物活性化合物。在分析大豆植株各部分时,使用固相萃取程序对提取物进行纯化。不同浓度的异黄酮苷元和糖苷以及不同基质的回收率为96 - 106%(总体相对标准偏差为2 - 9%)。根中的异黄酮浓度最高(12.5μg g⁻¹干重),而不同品种大豆中的含量约为3 - 1100μg g⁻¹鲜重。