黑龙江医药
黑龍江醫藥
흑룡강의약
HEILONGJIANG MEDICAL JOURNAL
2014年
1期
972-974,975
,共4页
贺国彬%李津明%赵金凤%武文强
賀國彬%李津明%趙金鳳%武文彊
하국빈%리진명%조금봉%무문강
双黄连口服液%质控成分%HPLC
雙黃連口服液%質控成分%HPLC
쌍황련구복액%질공성분%HPLC
Shuanghuanglian oral liquid%Quality control components%HPLC
目的:建立可同时测定双黄连口服液中黄芩苷、连翘苷、绿原酸,3种质控成分含量的HPLC方法.方法:色谱柱为Welchrom C18柱(4.6 mm×150 mm,5μm);流动相为甲醇(A)-0.2%磷酸(B)水溶液,梯度洗脱,分段变波长测定;柱温:30℃;体积流量1.0 mL/min。结果:3种成分的线性关系均良好,精密度、稳定性、重复性的RSD均低于2%,加样回收率为95%~120%。结论:本方法准确、灵敏、可靠,重现性较好,可用于双黄连口服液的质量控制。
目的:建立可同時測定雙黃連口服液中黃芩苷、連翹苷、綠原痠,3種質控成分含量的HPLC方法.方法:色譜柱為Welchrom C18柱(4.6 mm×150 mm,5μm);流動相為甲醇(A)-0.2%燐痠(B)水溶液,梯度洗脫,分段變波長測定;柱溫:30℃;體積流量1.0 mL/min。結果:3種成分的線性關繫均良好,精密度、穩定性、重複性的RSD均低于2%,加樣迴收率為95%~120%。結論:本方法準確、靈敏、可靠,重現性較好,可用于雙黃連口服液的質量控製。
목적:건립가동시측정쌍황련구복액중황금감、련교감、록원산,3충질공성분함량적HPLC방법.방법:색보주위Welchrom C18주(4.6 mm×150 mm,5μm);류동상위갑순(A)-0.2%린산(B)수용액,제도세탈,분단변파장측정;주온:30℃;체적류량1.0 mL/min。결과:3충성분적선성관계균량호,정밀도、은정성、중복성적RSD균저우2%,가양회수솔위95%~120%。결론:본방법준학、령민、가고,중현성교호,가용우쌍황련구복액적질량공제。
Objective:Estabilish a HPLC method which can masure the quality control compontent of baicalin SHL oral liquid, phillyrin and chlorogenic acid simultaneously. Methods:Chromatographic column:welchrom C18(4.6 mm×150 mm, 5μm);The mobile phase:an aqueous solution of methanol(A)-0.2%phosphoric acid(B),gradient elution, measure by segmentation variable wavelength;col-umn temperature:30℃;volume flow rate:1.0 mL/min. Results:the linear relationship of this three ingredient were all well and the RSD of precision, stability and repeatability were all less than 2%.The average recovery was 95%-120%. Conclusion:this method is accurate, sensitive, reliable and has a good reproducibility, can be used for quality control of Shuanghuanglian oral liquid.