化学分析计量
化學分析計量
화학분석계량
Chemical Analysis and Meterage
2015年
5期
62-64
,共3页
荀其宁%侯倩倩%刘志娟%许峰%张文申%刘霞%冀克俭
荀其寧%侯倩倩%劉誌娟%許峰%張文申%劉霞%冀剋儉
순기저%후천천%류지연%허봉%장문신%류하%기극검
黄芪%黄芪甲苷%液相色谱%蒸发光散射检测器
黃芪%黃芪甲苷%液相色譜%蒸髮光散射檢測器
황기%황기갑감%액상색보%증발광산사검측기
astragalous decoction pieces%astragaloside IV%HPLC%ELSD
采用蒸发光散射高效液相色谱法测定黄芪饮片中黄芪甲苷的含量。黄芪饮片分别用甲醇和正丁醇提取,以NaOH溶液洗涤,蒸干,再用甲醇溶解,采用Agilent SB–C18柱(250 mm×4.6 mm,5μm)分离测定,流动相为乙腈–水(32∶68),流量为1.0 mL/min,漂移管温度为80℃。方法检出限为1.5μg/mL,黄芪甲苷溶液的质量浓度在2~12μg/mL范围内与色谱峰面积线性关系良好(r2=0.9996),测定结果的相对标准偏差为0.65%(n=6),平均加标回收率为99.6%。该方法稳定可靠,可用于黄芪药材及其生物制品中黄芪甲苷含量的测定。
採用蒸髮光散射高效液相色譜法測定黃芪飲片中黃芪甲苷的含量。黃芪飲片分彆用甲醇和正丁醇提取,以NaOH溶液洗滌,蒸榦,再用甲醇溶解,採用Agilent SB–C18柱(250 mm×4.6 mm,5μm)分離測定,流動相為乙腈–水(32∶68),流量為1.0 mL/min,漂移管溫度為80℃。方法檢齣限為1.5μg/mL,黃芪甲苷溶液的質量濃度在2~12μg/mL範圍內與色譜峰麵積線性關繫良好(r2=0.9996),測定結果的相對標準偏差為0.65%(n=6),平均加標迴收率為99.6%。該方法穩定可靠,可用于黃芪藥材及其生物製品中黃芪甲苷含量的測定。
채용증발광산사고효액상색보법측정황기음편중황기갑감적함량。황기음편분별용갑순화정정순제취,이NaOH용액세조,증간,재용갑순용해,채용Agilent SB–C18주(250 mm×4.6 mm,5μm)분리측정,류동상위을정–수(32∶68),류량위1.0 mL/min,표이관온도위80℃。방법검출한위1.5μg/mL,황기갑감용액적질량농도재2~12μg/mL범위내여색보봉면적선성관계량호(r2=0.9996),측정결과적상대표준편차위0.65%(n=6),평균가표회수솔위99.6%。해방법은정가고,가용우황기약재급기생물제품중황기갑감함량적측정。
HPLC–ELSD method was used to determine astragalosideⅣ in astraglus decoction pieces. The sample of astragalous decoction pieces was extracted by methanol andn-butyl alchol, after cleaning with NaOH solution, the sample was dried and disolved in methanol, and was determined by Agilent SB–C18 column (250 mm×4.6 mm, 5μm), acetonitrile–water(32∶68) was as the mobile with theflow rate of 1.0 mL/min, the drifttube temperature was 80℃. The detection limit of the method was 1.5μg/mL. The linear range was 2–12μg/mL(r2=0.999 6). The RSD of determination results was 0.65%(n=6). The average recovery of astragalosideⅣ was 99.6%. This method is accurate, reliable and with good reproducibility, and it can be used for the determination of astragalosideⅣ in Radix Astragali and its products.