中南药学
中南藥學
중남약학
CENTRAL SOUTH PHARMACY
2009年
7期
499-502
,共4页
邓长凤%龚友兰%吴雪%向大位%欧阳丽娜%向大雄
鄧長鳳%龔友蘭%吳雪%嚮大位%歐暘麗娜%嚮大雄
산장봉%공우란%오설%향대위%구양려나%향대웅
葛根素%微乳%反相高效液相色谱法%血药浓度
葛根素%微乳%反相高效液相色譜法%血藥濃度
갈근소%미유%반상고효액상색보법%혈약농도
puerarin%microemulsion%RP-HPLC%plasma concentration
目的 建立反相高效液相色谱法测定大鼠血浆中的葛根素,用于葛根素微乳在大鼠体内的生物利用度研究.方法 取血浆样品,用乙腈沉淀蛋白,Phenomenex C18柱(250 mm×4.6 mm,5 μm)分离,4-羟基苯甲醛为内标,乙腈-0.1%醋酸溶液(23:77)为流动相,流速0.8 mL·min-1,紫外检测波长250 nm,柱温30 ℃,进样量 20 μL.结果 葛根素的线性范围为0.10~10.00 μg·mL-1(r=0.999 6),定量下限为0.10 μg·mL-1,提取回收率>79%,方法回收率>92%,日内、日间精密度RSD<6%.结论 本方法灵敏度好、准确性高,可用于大鼠血浆中葛根素浓度的测定以及葛根素微乳在大鼠体内的生物利用度研究.
目的 建立反相高效液相色譜法測定大鼠血漿中的葛根素,用于葛根素微乳在大鼠體內的生物利用度研究.方法 取血漿樣品,用乙腈沉澱蛋白,Phenomenex C18柱(250 mm×4.6 mm,5 μm)分離,4-羥基苯甲醛為內標,乙腈-0.1%醋痠溶液(23:77)為流動相,流速0.8 mL·min-1,紫外檢測波長250 nm,柱溫30 ℃,進樣量 20 μL.結果 葛根素的線性範圍為0.10~10.00 μg·mL-1(r=0.999 6),定量下限為0.10 μg·mL-1,提取迴收率>79%,方法迴收率>92%,日內、日間精密度RSD<6%.結論 本方法靈敏度好、準確性高,可用于大鼠血漿中葛根素濃度的測定以及葛根素微乳在大鼠體內的生物利用度研究.
목적 건립반상고효액상색보법측정대서혈장중적갈근소,용우갈근소미유재대서체내적생물이용도연구.방법 취혈장양품,용을정침정단백,Phenomenex C18주(250 mm×4.6 mm,5 μm)분리,4-간기분갑철위내표,을정-0.1%작산용액(23:77)위류동상,류속0.8 mL·min-1,자외검측파장250 nm,주온30 ℃,진양량 20 μL.결과 갈근소적선성범위위0.10~10.00 μg·mL-1(r=0.999 6),정량하한위0.10 μg·mL-1,제취회수솔>79%,방법회수솔>92%,일내、일간정밀도RSD<6%.결론 본방법령민도호、준학성고,가용우대서혈장중갈근소농도적측정이급갈근소미유재대서체내적생물이용도연구.
Objective To establish an RP-HPLC method for the determination of puerarin in rat plasma to be applied in the bioavailability study of puerarin microemulsion in rats.Methods Plasma samples were treated with acetonitrile to deposit proteins,and then were analyzed by HPLC on a Phenomenex C18 column(250 mm×4.6 mm,5 μm) using acetonitrile-0.1% acetic acid solution(23∶77)mixture solvent as the mobile phase at 0.8 mL·min-1.The column effluent was monitored by UV detector at 250 nm and 4-hydroxy-benzaldehyde was used as the internal standard.The column temperature was 30 ℃,and the injection volume was 20 μL.Results The calibration curve of puerarin in rat plasma at 0.10~10.00 μg·mL-1 was excellently linear(r=0.999 6),with the lower limit of quantification of 0.10 μg·mL-1.The extraction recoveries were larger than 79%,the method recoveries larger than 92%,and the intra- and inter-day RSD smaller than 6%.Conclusion The validated method is sensitive,accurate and suitable for the determination of puerarin in rat plasma and bioavailability study of puerarin microemulsion in rats.