中医药导报
中醫藥導報
중의약도보
GUIDING JOURNAL OF TCM
2013年
8期
82-84
,共3页
郭爱枝%何益峰%王吉慧%孙培文
郭愛枝%何益峰%王吉慧%孫培文
곽애지%하익봉%왕길혜%손배문
丹路口服液%薄层色谱法%高效液相色谱法%芍药苷
丹路口服液%薄層色譜法%高效液相色譜法%芍藥苷
단로구복액%박층색보법%고효액상색보법%작약감
Danlu Oral Liquid%TLC%HPLC%Paeoniflorin
目的:建立丹路口服液质量标准。方法:采用TLC法对丹路口服液中丹参、当归、川芎、红花进行定性鉴别;以HPLC法对其赤芍中的芍药苷进行含量测定。色谱柱:Symmetry C18柱(200 mm×4.6 mm,5μm);流动相:乙腈-1‰磷酸水溶液(19∶81);流速:1.0 mL·min-1;检测波长:230 nm;柱温:30℃。结果:在TLC色谱中检出丹参、当归、川芎、红花;芍药苷进样量在6.14-61.40μg mL-1范围内线性关系良好,r=0.9998;平均加样回收率101.0%,RSD%为2.5%。结论:所建立的方法简便可行,重现性好,为丹路口服液质量控制提供了方法。
目的:建立丹路口服液質量標準。方法:採用TLC法對丹路口服液中丹參、噹歸、川芎、紅花進行定性鑒彆;以HPLC法對其赤芍中的芍藥苷進行含量測定。色譜柱:Symmetry C18柱(200 mm×4.6 mm,5μm);流動相:乙腈-1‰燐痠水溶液(19∶81);流速:1.0 mL·min-1;檢測波長:230 nm;柱溫:30℃。結果:在TLC色譜中檢齣丹參、噹歸、川芎、紅花;芍藥苷進樣量在6.14-61.40μg mL-1範圍內線性關繫良好,r=0.9998;平均加樣迴收率101.0%,RSD%為2.5%。結論:所建立的方法簡便可行,重現性好,為丹路口服液質量控製提供瞭方法。
목적:건립단로구복액질량표준。방법:채용TLC법대단로구복액중단삼、당귀、천궁、홍화진행정성감별;이HPLC법대기적작중적작약감진행함량측정。색보주:Symmetry C18주(200 mm×4.6 mm,5μm);류동상:을정-1‰린산수용액(19∶81);류속:1.0 mL·min-1;검측파장:230 nm;주온:30℃。결과:재TLC색보중검출단삼、당귀、천궁、홍화;작약감진양량재6.14-61.40μg mL-1범위내선성관계량호,r=0.9998;평균가양회수솔101.0%,RSD%위2.5%。결론:소건립적방법간편가행,중현성호,위단로구복액질량공제제공료방법。
Objective: To establish a quality standard for Danlu Oral Liquid. Methods: Salvia mihiorrhiza Bge, Angelica sinensis(Oliv) Diels, Ligustici Chuanxiong Hort, Carthamus tinctorius L were indentified by TLC. HPLC was applied to deter-mine the Paeoniflorin;The separation was performed on a Symmetry of C18 column(200 mm×4.6 nnn, 5μm); The mobile phase was consisted of acetonitrile and water(1‰ phosphoric acid)(19∶81); The detection wavelength was 230 nm; Flow rate was 1.0 mL·min-1; Column temperature was 30℃. Results: Salvia miltiorrhiza Bge, Angelica sinensis(Oliv) Diels, Ligusticum chuanxiong Hort, Carthamus tinctorius L could be detected by TLC. Paeoniflorin showed a good linear relationship at 6.14-61.40 μg·mL-1, r=0.9998; The average recovery of the added index was 101.0%, and RSD% was 2.5%. Conclusion: The method is simple, feasible and reproducible. The established quality standard can be used for the quality control of this medicine.