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METHOD FOR ANALYZING MEDICINAL COMPONENTS OF GINSENG

机译:人参药材成分分析方法

摘要

PURPOSE:To analyze ginseside with high sensitivity without receiving the effect of impure components, by converting ginseside to sugar by hydrolysis using and acid and detecting sugar by a fluorescent method. CONSTITUTION:One end of a separation column 1 is connected to a mobilie phase tank 3 through a specimen injection port 2 and the other end thereof is connected to an acid liquid tank 4 for hydrolysis and further connected to a phosphorating reagent liquid tank 6 through a mixing coil 5. A fluorescence detector 8 is connected to the tank 6 on the outflow side thereof through a cooling tank 7. Acetonitrile and water are received in the tank 3 and an aqueous perchloric acid solution is received in the tank 4 and an aqueous L-alginic acid solution is received in the tank 6 to operate an apparatus. When a specimen is injected, ginseside of a specimen component is separated as a fixed phase and subsequently receives hydrolysis by perchloric acid to be converted to sugar. This sugar is phosphorated by the phosphorating reagent to flow in the detector 8 and emits the fluorescence proportional to concn. Since the other sugar component in the specimen is separated from the ginseside component by the column 1, said sugar does not obstruct analysis.
机译:目的:通过用酸和酸水解将人参皂甙转化为糖,并通过荧光法检测糖,从而以高灵敏度分析人参皂甙而不受到不纯成分的影响。组成:分离柱1的一端通过标本注入口2连接到流动相罐3,另一端连接到用于水解的酸液罐4,并进一步通过分离管1连接到磷化试剂液罐6。混合线圈5。荧光检测器8通过冷却罐7连接至罐6的流出侧。乙腈和水被容纳在罐3中,高氯酸水溶液被容纳在罐4中,水L -藻酸溶液被接收在罐6中以操作设备。注入标本时,标本成分的人参皂苷被分离为固定相,随后被高氯酸水解而转化为糖。该糖被磷化试剂磷化以在检测器8中流动并且发射与concn成比例的荧光。由于样品中的其他糖成分已通过柱1与人参皂甙成分分离,因此该糖不会妨碍分析。

著录项

  • 公开/公告号JPS63193039A

    专利类型

  • 公开/公告日1988-08-10

    原文格式PDF

  • 申请/专利权人 SHIMADZU CORP;

    申请/专利号JP19870026026

  • 发明设计人 OKADA EIJI;HAMADA NAOKI;

    申请日1987-02-06

  • 分类号G01N31/00;G01N21/64;G01N21/77;G01N30/88;G01N33/15;

  • 国家 JP

  • 入库时间 2022-08-22 07:03:29

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