中国药业
中國藥業
중국약업
CHINA PHARMACEUTICALS
2015年
16期
52-53
,共2页
付智慧%陆锦锐%李淑军%胡慧华
付智慧%陸錦銳%李淑軍%鬍慧華
부지혜%륙금예%리숙군%호혜화
骆驼蓬碱%骆驼蓬%炮制
駱駝蓬堿%駱駝蓬%砲製
락타봉감%락타봉%포제
barmaline%Peganumharmala L.%processing
目的:采用高效液相色谱(HPLC)法测定炮制前后骆驼蓬中骆驼蓬碱的含量变化。方法色谱柱为 Agilent SB 柱(250 mm ×4.6 mm,5μm),流动相为甲醇-0.02 mol/L硫酸铵(32:68,V/ V),流速为1.0 mL/min,柱温为25℃,检测波长为375 nm。结果炮制前后骆驼蓬中骆驼蓬碱的平均含量分别为2.72,1.90 mg/g,炮制后的骆驼蓬碱含量较炮制前下降了30.15%。结论骆驼蓬经红酒煮制后,骆驼蓬碱含量可显著降低。
目的:採用高效液相色譜(HPLC)法測定砲製前後駱駝蓬中駱駝蓬堿的含量變化。方法色譜柱為 Agilent SB 柱(250 mm ×4.6 mm,5μm),流動相為甲醇-0.02 mol/L硫痠銨(32:68,V/ V),流速為1.0 mL/min,柱溫為25℃,檢測波長為375 nm。結果砲製前後駱駝蓬中駱駝蓬堿的平均含量分彆為2.72,1.90 mg/g,砲製後的駱駝蓬堿含量較砲製前下降瞭30.15%。結論駱駝蓬經紅酒煮製後,駱駝蓬堿含量可顯著降低。
목적:채용고효액상색보(HPLC)법측정포제전후락타봉중락타봉감적함량변화。방법색보주위 Agilent SB 주(250 mm ×4.6 mm,5μm),류동상위갑순-0.02 mol/L류산안(32:68,V/ V),류속위1.0 mL/min,주온위25℃,검측파장위375 nm。결과포제전후락타봉중락타봉감적평균함량분별위2.72,1.90 mg/g,포제후적락타봉감함량교포제전하강료30.15%。결론락타봉경홍주자제후,락타봉감함량가현저강저。
Objective To investigate tbe cbange of barmaline content in Peganumharmala L. before and after processing by adopting tbe HPLC metbod. Methods Tbe determination was carried out witb tbe Agilent SB column(250 mm × 4. 6 mm,5 μm);tbe mobile pbase consisted of metbanol-0. 02 mol/L ammonium sulfate(32:68,V/ V)for elution;tbe detection wavelengtb was set at 375 nm,and tbe flow rate was 1. 0 mL/min at tbe column temperature of 25 ℃. Results Tbe average barmaline content of crude Peganumharmala L. was 2. 72 mg/g,tbe average barmaline contents in Peganumharmala L. before and after processing were 2. 72,1. 9 mg/g,respective-ly,tbe barmaline content after processing was decreased by 30. 15% tban before processing. Conclusion Tbe content of barmaline in Peganumharmala L. after decocting witb red wine is significantly reduced.