Faculty of Pharmacy, Keio University, 1-5-30 Shibakoen, Minato-ku, Tokyo, 105-8512, Japan.
Research Center for Medicinal Plant Resources, National Institutes of Biomedical Innovation, Health and Nutrition, 1-2 Hachimandai, Tsukuba, Ibaraki, 305-0843, Japan.
J Nat Med. 2020 Jan;74(1):135-141. doi: 10.1007/s11418-019-01355-y. Epub 2019 Aug 12.
LC-MS analyses of saponin fractions of Achyranthes roots in the Japanese market revealed that there were three patterns for the saponin fraction of their water extracts, i.e., the saponins with a sugar moiety at position 28 [achyranthosides B (3), C (4) and D (5)] were the major constituents, the saponins without sugar moiety at position 28 [betavulgarosides II (10) and IV (11)] were the major constituents, and mixtures of these saponins. In a decoction prepared from the sample which contained 10 and 11 as the major saponins, their amounts were largely decreased compared with those of the water extract. As large amounts of these saponins were found in the precipitates formed by heating of the water extract, these saponins were seemed to precipitate out under heating. When hot water was used for the extraction, 3, 4 and 5 were detected even from the samples whose water extract did not contain these saponins. This was attributed to inhibition of endogenous esterase which hydrolyzes the ester linkage at position 28. When saponins were extracted with reagent grade 1-butanol, in addition to the decrease of the amounts of highly polar saponins, oxidative decarboxylation of 3 and 10 occurred resulting in formation of achyranthoside E (6) and spinacoside D (12), respectively. As these changes were not observed with HPLC grade 1-butanol, which contain not more than 5 ppm of peroxide impurities, the change was attributable to the peroxide impurities contained in the reagent grade 1-butanol.
LC-MS 分析日本市场中牛膝根的皂苷部分,发现其水提取物的皂苷部分有三种模式,即 28 位带有糖基的皂苷(achyranthosides B (3)、C (4) 和 D (5))为主要成分、28 位不带糖基的皂苷(betavulgarosides II (10) 和 IV (11))为主要成分,以及这些皂苷的混合物。在由主要含有 10 和 11 的样品制成的煎剂中,其含量与水提取物相比大大减少。由于这些皂苷在水提取物加热形成的沉淀中大量存在,因此这些皂苷似乎在加热下沉淀出来。当热水用于提取时,即使在水提取物中不含有这些皂苷的样品中,也检测到了 3、4 和 5。这归因于抑制了在 28 位水解酯键的内源性酯酶。当用试剂级 1-丁醇提取皂苷时,除了高极性皂苷的含量减少外,3 和 10 还发生了氧化脱羧反应,分别形成了 achyranthoside E (6) 和 spinacoside D (12)。由于这些变化在 HPLC 级 1-丁醇中没有观察到,HPLC 级 1-丁醇中过氧化物杂质含量不超过 5 ppm,因此这种变化归因于试剂级 1-丁醇中所含的过氧化物杂质。