北方药学
北方藥學
북방약학
JOURNAL OF NORTH PHARMACY
2014年
1期
1-2,3
,共3页
齐翠翠%李竞%高英%李卫民%周海平%孔增科
齊翠翠%李競%高英%李衛民%週海平%孔增科
제취취%리경%고영%리위민%주해평%공증과
连翘%连翘苷%连翘酯苷A%高效液相色谱法
連翹%連翹苷%連翹酯苷A%高效液相色譜法
련교%련교감%련교지감A%고효액상색보법
Forsythia suspense%Phillyrin%Forsythoside A%HPLC
目的:采用HPLC法测定太行山区不同产地、不同采集时间连翘中连翘苷及连翘酯苷A的含量。方法:采用Agilent ZORBAX Eclipse XDB-C18(250mm×4.6mm,5μm)色谱柱,测定连翘苷以乙腈-水(25∶75)为流动相,等度洗脱;流速为1.0ml·min-1;检测波长为277nm。测定连翘酯苷A以乙腈-0.4%冰醋酸溶液(15∶85)为流动相,等度洗脱,流速为1.0ml·min-1;检测波长为330nm。结果:连翘苷和连翘酯苷A线性范围分别为0.206~2.060μg和0.120~1.200μg,平均回收率分别为99.52%(RSD=1.74%)和99.63%(RSD=1.21%)。结论:太行山区不同产地连翘中连翘苷和连翘酯苷A含量差异较大,7月份采集连翘中连翘苷、连翘酯苷A含量最高。含量测定方法准确、快速,适用于连翘的质量控制。
目的:採用HPLC法測定太行山區不同產地、不同採集時間連翹中連翹苷及連翹酯苷A的含量。方法:採用Agilent ZORBAX Eclipse XDB-C18(250mm×4.6mm,5μm)色譜柱,測定連翹苷以乙腈-水(25∶75)為流動相,等度洗脫;流速為1.0ml·min-1;檢測波長為277nm。測定連翹酯苷A以乙腈-0.4%冰醋痠溶液(15∶85)為流動相,等度洗脫,流速為1.0ml·min-1;檢測波長為330nm。結果:連翹苷和連翹酯苷A線性範圍分彆為0.206~2.060μg和0.120~1.200μg,平均迴收率分彆為99.52%(RSD=1.74%)和99.63%(RSD=1.21%)。結論:太行山區不同產地連翹中連翹苷和連翹酯苷A含量差異較大,7月份採集連翹中連翹苷、連翹酯苷A含量最高。含量測定方法準確、快速,適用于連翹的質量控製。
목적:채용HPLC법측정태행산구불동산지、불동채집시간련교중련교감급련교지감A적함량。방법:채용Agilent ZORBAX Eclipse XDB-C18(250mm×4.6mm,5μm)색보주,측정련교감이을정-수(25∶75)위류동상,등도세탈;류속위1.0ml·min-1;검측파장위277nm。측정련교지감A이을정-0.4%빙작산용액(15∶85)위류동상,등도세탈,류속위1.0ml·min-1;검측파장위330nm。결과:련교감화련교지감A선성범위분별위0.206~2.060μg화0.120~1.200μg,평균회수솔분별위99.52%(RSD=1.74%)화99.63%(RSD=1.21%)。결론:태행산구불동산지련교중련교감화련교지감A함량차이교대,7월빈채집련교중련교감、련교지감A함량최고。함량측정방법준학、쾌속,괄용우련교적질량공제。
Objective:To establish an HPLC method for the determination of phillyrin and Forsythia-side A in Forsythia suspense from different sites and gathering periods in Taihang mountain. Methods:Agilent ZORBAX Eclipse XDB-C18 (250mm×4.6mm,5μm) was applied. For determina-tion of phillyrin,Mobile phase was with acetonitrile-water (25∶75), the separation was carried out with a gradient program at a flow rate of 1.0ml·min-1 and detection wavelength was 277nm. For determination of Forsythoside A, Mobile phase was with acetonitrile-0.4%acetic acid Solution(15∶85),the separation was carried out with a gradient program at a flow rate of 1.0ml·min-1 and detection wavelength was 330nm. Results:Phillyrin and Forsythiaside A showed good linearity in the ranges of 0.206~2.060μg and 0.120~1.200μg with average recoveries of 99.52% and 99.63%,Respectively. Conclusions:The contents of phillyrin and Forsythiaside A in Forsythia suspensa from different sites in Taihang mountain marked difference, the contents of phillyrin and Forsythiaside A in Forsythia suspense was the highest in July,the method is simple and rapid for determination the contents of phillyrin and Forsythiaside A in Forsythia suspense,and can be used as the quality control of Forsythia suspensa.