中国药物经济学
中國藥物經濟學
중국약물경제학
CHINA JOURNAL OF PHARMACEUTICAL ECONOMICS
2014年
7期
14-17
,共4页
复方血栓通%三七皂苷R1%人参皂苷Rg1%人参皂苷Re%人参皂苷Rb1%通用检测方法
複方血栓通%三七皂苷R1%人參皂苷Rg1%人參皂苷Re%人參皂苷Rb1%通用檢測方法
복방혈전통%삼칠조감R1%인삼조감Rg1%인삼조감Re%인삼조감Rb1%통용검측방법
Fufang XueShuanTong preparations%Notoginsenoside R1%Ginsenoside Rg1%Ginsenoside Re%Ginsenoside Rb1%Universal Method for the Determination
目的:统一复方血栓通颗粒、片、滴丸和软胶囊中三七皂苷R1、人参皂苷Rg1、人参皂苷Re和人参皂苷Rb1的含量测定方法。方法采用高效液相色谱法,使用Thermo ODS2(5μm,150.0 mm×4.6 mm)色谱柱,柱温为20℃,以乙腈-水为流动相进行梯度洗脱,流速为1.0 ml/min,检测波长为203 nm。结果三七皂苷R1在0.0518~2.5900(r=0.9996)、人参皂苷Rg1在0.2090~8.3588(r=0.9991)、人参皂苷Re在0.0507~2.5371(r=0.9990)、人参皂苷Rb1在0.2044~8.1752(r=0.9995)范围内与峰面积线性关系良好;精密度、重复性、稳定性及加样回收率结果均能满足分析要求。结论该方法简单可行,为复方血栓通品种中三七皂苷R1、人参皂苷Rg1、人参皂苷Re和人参皂苷Rb1含量测定方法的统一提供了可靠的依据。
目的:統一複方血栓通顆粒、片、滴汍和軟膠囊中三七皂苷R1、人參皂苷Rg1、人參皂苷Re和人參皂苷Rb1的含量測定方法。方法採用高效液相色譜法,使用Thermo ODS2(5μm,150.0 mm×4.6 mm)色譜柱,柱溫為20℃,以乙腈-水為流動相進行梯度洗脫,流速為1.0 ml/min,檢測波長為203 nm。結果三七皂苷R1在0.0518~2.5900(r=0.9996)、人參皂苷Rg1在0.2090~8.3588(r=0.9991)、人參皂苷Re在0.0507~2.5371(r=0.9990)、人參皂苷Rb1在0.2044~8.1752(r=0.9995)範圍內與峰麵積線性關繫良好;精密度、重複性、穩定性及加樣迴收率結果均能滿足分析要求。結論該方法簡單可行,為複方血栓通品種中三七皂苷R1、人參皂苷Rg1、人參皂苷Re和人參皂苷Rb1含量測定方法的統一提供瞭可靠的依據。
목적:통일복방혈전통과립、편、적환화연효낭중삼칠조감R1、인삼조감Rg1、인삼조감Re화인삼조감Rb1적함량측정방법。방법채용고효액상색보법,사용Thermo ODS2(5μm,150.0 mm×4.6 mm)색보주,주온위20℃,이을정-수위류동상진행제도세탈,류속위1.0 ml/min,검측파장위203 nm。결과삼칠조감R1재0.0518~2.5900(r=0.9996)、인삼조감Rg1재0.2090~8.3588(r=0.9991)、인삼조감Re재0.0507~2.5371(r=0.9990)、인삼조감Rb1재0.2044~8.1752(r=0.9995)범위내여봉면적선성관계량호;정밀도、중복성、은정성급가양회수솔결과균능만족분석요구。결론해방법간단가행,위복방혈전통품충중삼칠조감R1、인삼조감Rg1、인삼조감Re화인삼조감Rb1함량측정방법적통일제공료가고적의거。
Objective To unified the method for the content determination of Notoginsenoside R1,Ginsenoside Rg1,Ginsenoside Re,Ginsenoside Rb1 of Fufang Xueshuantong granules,tablets,dripping pils and soft capsules. Methods By HPLC method;Notoginsenoside R1,Ginsenoside Rg1,Ginsenoside Re,Ginsenoside Rb1were analyzed on an Thermo ODS2(5 μm,150.0 mm×4.6 mm)column at 20℃;The gradient elution was acetonitrile-water at the flow rate of 1.0ml/min;The detection wavelength was 203 nm.Results Notoginsenoside R1,Ginsenoside Rg1,Ginsenoside Re,Ginsenoside Rb1 al have good linearity in the range of 0.0518~2.5900(r=0.9996),0.2090~8.3588(r=0.9991), 0.0507~2.5371(r=0.9990),0.2044~8.1752(r=0.9995)with satisfied precision,repetition,stability and recovery.Conclusion This method is simple,feasible,and can offer the reliable basis for unification of the standards.