医药前沿
醫藥前沿
의약전연
YIAYAO QIANYAN
2013年
32期
95-96
,共2页
韦浪%杨日芳%李桃山%王娜%梁永赞%何胜%张树球(通讯作者)
韋浪%楊日芳%李桃山%王娜%樑永讚%何勝%張樹毬(通訊作者)
위랑%양일방%리도산%왕나%량영찬%하성%장수구(통신작자)
高效液相色谱(HPLC)%海尔福口服液%甘草酸
高效液相色譜(HPLC)%海爾福口服液%甘草痠
고효액상색보(HPLC)%해이복구복액%감초산
HPLC%Hai er fu oral liquid%Glycyrrhizic acid
目的:采用高效液相色谱(HPLC)测定海尔福口服液中甘草酸含量,并与甘草药材提取液进行对比分析。方法采用高效液相色谱法,色谱柱:Acclaim?120 C185μm (4.6×250mm)流动相:甲醇-水-冰乙酸(71:28:1)波长:250nm 流速:1.0ml/min。结果(1)甘草药材1醇提液甘草酸含量为28.900±0.221 mg/g生药;(2)甘草药材1水提液甘草酸为19.360±0.029mg/g生药;(3)旧甘草药材水提液甘草酸含量为13.217±0.064mg/g生药;(4)海尔福口服液中甘草酸含量为11.887±0.186mg/g生药;(5)甘草药材2水提液甘草酸为25.907±0.619mg/g生药;各样品甘草酸含量比较,p<0.01,差异均有统计学意义;加样回收试验平均为109.88%,进样20μl测定浓度在0.04-0.32m g/m l按峰高值计有良好线性关系,相关系数为R=0.9984,精密度RSD%=0.45%。结论该法测定准确,线性关系好,可用于海尔福口服液质量控制.
目的:採用高效液相色譜(HPLC)測定海爾福口服液中甘草痠含量,併與甘草藥材提取液進行對比分析。方法採用高效液相色譜法,色譜柱:Acclaim?120 C185μm (4.6×250mm)流動相:甲醇-水-冰乙痠(71:28:1)波長:250nm 流速:1.0ml/min。結果(1)甘草藥材1醇提液甘草痠含量為28.900±0.221 mg/g生藥;(2)甘草藥材1水提液甘草痠為19.360±0.029mg/g生藥;(3)舊甘草藥材水提液甘草痠含量為13.217±0.064mg/g生藥;(4)海爾福口服液中甘草痠含量為11.887±0.186mg/g生藥;(5)甘草藥材2水提液甘草痠為25.907±0.619mg/g生藥;各樣品甘草痠含量比較,p<0.01,差異均有統計學意義;加樣迴收試驗平均為109.88%,進樣20μl測定濃度在0.04-0.32m g/m l按峰高值計有良好線性關繫,相關繫數為R=0.9984,精密度RSD%=0.45%。結論該法測定準確,線性關繫好,可用于海爾福口服液質量控製.
목적:채용고효액상색보(HPLC)측정해이복구복액중감초산함량,병여감초약재제취액진행대비분석。방법채용고효액상색보법,색보주:Acclaim?120 C185μm (4.6×250mm)류동상:갑순-수-빙을산(71:28:1)파장:250nm 류속:1.0ml/min。결과(1)감초약재1순제액감초산함량위28.900±0.221 mg/g생약;(2)감초약재1수제액감초산위19.360±0.029mg/g생약;(3)구감초약재수제액감초산함량위13.217±0.064mg/g생약;(4)해이복구복액중감초산함량위11.887±0.186mg/g생약;(5)감초약재2수제액감초산위25.907±0.619mg/g생약;각양품감초산함량비교,p<0.01,차이균유통계학의의;가양회수시험평균위109.88%,진양20μl측정농도재0.04-0.32m g/m l안봉고치계유량호선성관계,상관계수위R=0.9984,정밀도RSD%=0.45%。결론해법측정준학,선성관계호,가용우해이복구복액질량공제.
Objective Determination of Glycyrrhizic acid content in Hai er fu oral liquid by HPLC, and comparative analysis with Licorice extract. Method Using high-performance liquid chromatography, the determination was performed on an Acclaim? 120 C18 5 μm (4.6×250mm) column, with the mobile phase was methanol - water -glacial acetic acid (71:28:1) at a flow rate of 1.0ml/min, and the detection wavelength was 250 nm. Result (1) The Glycyrrhizic acid content of Licorice 1 alcohol extract was 28.900±0.221 mg/g crude drug;(2) The water extract of licorice 1 Glycyrrhizic acid was 19.360±0.029mg/g crude drug ;(3) The Glycyrrhizic acid content of old licorice extract was 13.217±0.064mg/g crude drug;(4) The content of Glycyrrhizic acid in Hai er fu oral liquid was 11.887± 0.186mg/g crude drug;(5) The water extract of licorice 2 Glycyrrhizic acid was 25.907±0.619mg/g crude drug; compared the content of Glycyrrhizic acid in al samples, p<0.01, the differences were statisticaly significant; The results of recovery test for an average of 109.88%, Determination of the concentration of 20 μ l at 0.04- 0.32mg/ml according to the peak value meter had a good linear relationship between the sample, The correlation coefficient was R=0.9984, The precision of RSD% was 0.45%. Conclusion: This method has accurate determination and good linear relationship, can be used for the quality control of Hai er fu oral liquid.