中国药学(英文版)
中國藥學(英文版)
중국약학(영문판)
JOURNAL OF CHINESE PHARMACEUTICAL SCIENCES
2006年
2期
121-126
,共6页
刘火安%王伯初%戴传云%邵志勇%何从林%贾云
劉火安%王伯初%戴傳雲%邵誌勇%何從林%賈雲
류화안%왕백초%대전운%소지용%하종림%가운
葛根%总黄酮%大孔树脂%分离与纯化
葛根%總黃酮%大孔樹脂%分離與純化
갈근%총황동%대공수지%분리여순화
Radix Puerariae%total flavonoids%macroporous resin%separation%purification
目的筛选分离葛根总黄酮的最佳树脂,并对影响分离的各种因素进行系统的研究,使纯化工艺达到最优.方法采用静态与动态的吸附-解吸两种方法,利用紫外可见分光光度计测量葛根总黄酮的含量,研究不同大孔吸附树脂及其不同的工艺条件对总黄酮分离纯化的影响.结果SP70分离效果最好,其最佳工艺为药液浓度0.5 g·mL-1(相当于原生药)、pH为5-6、以2 BV·h-1速率进行上样,上样量为60BV,以5 BV的70%乙醇、2 BV·h-1的流速进行洗脱,效果最佳.经SP70处理后的葛根总黄酮的含量可达80%以上.结论大孔吸附树脂SP70分离纯化总黄酮效果较好,适合工业生产.
目的篩選分離葛根總黃酮的最佳樹脂,併對影響分離的各種因素進行繫統的研究,使純化工藝達到最優.方法採用靜態與動態的吸附-解吸兩種方法,利用紫外可見分光光度計測量葛根總黃酮的含量,研究不同大孔吸附樹脂及其不同的工藝條件對總黃酮分離純化的影響.結果SP70分離效果最好,其最佳工藝為藥液濃度0.5 g·mL-1(相噹于原生藥)、pH為5-6、以2 BV·h-1速率進行上樣,上樣量為60BV,以5 BV的70%乙醇、2 BV·h-1的流速進行洗脫,效果最佳.經SP70處理後的葛根總黃酮的含量可達80%以上.結論大孔吸附樹脂SP70分離純化總黃酮效果較好,適閤工業生產.
목적사선분리갈근총황동적최가수지,병대영향분리적각충인소진행계통적연구,사순화공예체도최우.방법채용정태여동태적흡부-해흡량충방법,이용자외가견분광광도계측량갈근총황동적함량,연구불동대공흡부수지급기불동적공예조건대총황동분리순화적영향.결과SP70분리효과최호,기최가공예위약액농도0.5 g·mL-1(상당우원생약)、pH위5-6、이2 BV·h-1속솔진행상양,상양량위60BV,이5 BV적70%을순、2 BV·h-1적류속진행세탈,효과최가.경SP70처리후적갈근총황동적함량가체80%이상.결론대공흡부수지SP70분리순화총황동효과교호,괄합공업생산.
Aim To screen the optimum macroporous resin and conditions for the isolation and purification of flavonoids from Radix Puerariae. Methods The static and dynamic adsorption/desorption methods were used, and the separation and purification process was evaluated by measuring the concentration of total flavonoid in the fractions with UV spectrophotometer. Results The SP70 macroporous resin was the most effective compared with other macroporous resins. The optimum conditions were screened, which were 0. 5 g· mL- 1 corresponding to crude drug for concentration of extract, pH 5 - 6, and appended 60 times the volume of the resin bed (BV) with the adsorption speed 2 BV· h - 1,and the volume of aq. 70% (V/V) ethanol as eluant was 5 BV with desorption speed 2 BV·h-1. By this method, the final contents of total flavonoids exceeded 80%. Conclusion The SP70 macroporousresin is the most effective one for large-scale isolation and purification of flavonoids from Radix Pueraria, which meets industrial needs.