西北药学杂志
西北藥學雜誌
서북약학잡지
2014年
5期
441-443
,共3页
卢翠婷%冯晓华%郭波红%卫世杰%李宁
盧翠婷%馮曉華%郭波紅%衛世傑%李寧
로취정%풍효화%곽파홍%위세걸%리저
微乳液相色谱法%丹参%隐丹参酮%丹参酮ⅡA
微乳液相色譜法%丹參%隱丹參酮%丹參酮ⅡA
미유액상색보법%단삼%은단삼동%단삼동ⅡA
microemulsion liquid chromatography(MELC)%Salvia miltiorrhiza%cryptotanshinone%tanshinone ⅡA
目的:建立丹参中隐丹参酮和丹参酮Ⅱ A 的含量测定方法。方法采用微乳液相色谱法。色谱柱:Diamonsal C18(250 mm ×4.6 mm ,5μm);流动相:0.14 mol · L -1十二烷基硫酸钠-1.08 mol · L -1正丁醇-0.070 mol · L -1正辛烷-水微乳;流速:0.7 mL · min-1;柱温:室温;检测波长:270 nm。结果隐丹参酮和丹参酮ⅡA分别在0.962~38.48和1.022~40.88μg范围内线性关系良好,相关系数 r>0.9995;平均加样回收率(n=6)分别为96.5%和97.2%,RSD分别为2.71%和1.69%。结论该方法准确,简单易行,可用于丹参药材中2种有效成分的含量分析。
目的:建立丹參中隱丹參酮和丹參酮Ⅱ A 的含量測定方法。方法採用微乳液相色譜法。色譜柱:Diamonsal C18(250 mm ×4.6 mm ,5μm);流動相:0.14 mol · L -1十二烷基硫痠鈉-1.08 mol · L -1正丁醇-0.070 mol · L -1正辛烷-水微乳;流速:0.7 mL · min-1;柱溫:室溫;檢測波長:270 nm。結果隱丹參酮和丹參酮ⅡA分彆在0.962~38.48和1.022~40.88μg範圍內線性關繫良好,相關繫數 r>0.9995;平均加樣迴收率(n=6)分彆為96.5%和97.2%,RSD分彆為2.71%和1.69%。結論該方法準確,簡單易行,可用于丹參藥材中2種有效成分的含量分析。
목적:건립단삼중은단삼동화단삼동Ⅱ A 적함량측정방법。방법채용미유액상색보법。색보주:Diamonsal C18(250 mm ×4.6 mm ,5μm);류동상:0.14 mol · L -1십이완기류산납-1.08 mol · L -1정정순-0.070 mol · L -1정신완-수미유;류속:0.7 mL · min-1;주온:실온;검측파장:270 nm。결과은단삼동화단삼동ⅡA분별재0.962~38.48화1.022~40.88μg범위내선성관계량호,상관계수 r>0.9995;평균가양회수솔(n=6)분별위96.5%화97.2%,RSD분별위2.71%화1.69%。결론해방법준학,간단역행,가용우단삼약재중2충유효성분적함량분석。
Objective To develop an MELC method for determining cryptotanshinone and tanshinone in Salviamiltiorrhiza simulta-neously .Methods A Diamonsil C18 column (250 mm × 4 .6 mm ,5 μm) was used ,and the mobile phase consisted of 0 .14 mol · L-1 SDS-1 .08 mol · L -1 n-butanol-0 .070 mol · L -1 n-octane-water at a flow rate of 0 .7 mL · min-1 .The column temperature was room temperature ,and the detection wavelength was set at 270 nm .Results The linear range of cryptotanshinone and tanshinoneⅡA were within 0 .962-38 .48 and 1 .022-40 .88 μg ,respectively .The correlation coefficient r were 0 .999 5 and 0 .999 8 ,respec-tively .The average recoveries (n=6) were 96 .5% with RSD=2 .71% (n=6) and 97 .2% with RSD=1 .69% (n=6) .Conclu-sion This method was simple ,accurate and reliable ,and could be applied in the determination of the two components in Salvia miltiorrhiz a .