中国中医药信息杂志
中國中醫藥信息雜誌
중국중의약신식잡지
Chinese Journal of Information on Traditional Chinese Medicine
2015年
11期
86-88
,共3页
余双英%刘绣华%张凤%朴淑娟%陆文铨
餘雙英%劉繡華%張鳳%樸淑娟%陸文銓
여쌍영%류수화%장봉%박숙연%륙문전
复方沙塔干口服液%阿魏酸%高效液相色谱法%薄层色谱法%质量标准
複方沙塔榦口服液%阿魏痠%高效液相色譜法%薄層色譜法%質量標準
복방사탑간구복액%아위산%고효액상색보법%박층색보법%질량표준
compound Shatagan Oral Liquid%ferulic acid%HPLC%TLC%quality standard
目的 建立复方沙塔干口服液的质量标准.方法 采用薄层色谱法对该制剂中的君药川芎进行专属性鉴别;采用高效液相色谱法对川芎中有效成分阿魏酸进行含量测定.色谱柱:Diamonsil C18柱(4.6 mm×250 mm, 5μm);流动相:甲醇-1%冰醋酸,梯度洗脱(0~5 min,35%甲醇;5~8 min,35%→23%甲醇;8~22 min,23%甲醇);检测波长:322 nm;流速:1.0 mL/min;柱温:30 ℃;进样量:5μL.结果 阿魏酸进样量在0.039 4~0.630 0μg范围内线性关系良好(r=0.999 7,n=7),平均加样回收率为98.22%,RSD=2.62%(n=6).结论 本研究所建立的质量标准结果准确,灵敏度高,重复性良好,可用于复方沙塔干口服液的质量控制.
目的 建立複方沙塔榦口服液的質量標準.方法 採用薄層色譜法對該製劑中的君藥川芎進行專屬性鑒彆;採用高效液相色譜法對川芎中有效成分阿魏痠進行含量測定.色譜柱:Diamonsil C18柱(4.6 mm×250 mm, 5μm);流動相:甲醇-1%冰醋痠,梯度洗脫(0~5 min,35%甲醇;5~8 min,35%→23%甲醇;8~22 min,23%甲醇);檢測波長:322 nm;流速:1.0 mL/min;柱溫:30 ℃;進樣量:5μL.結果 阿魏痠進樣量在0.039 4~0.630 0μg範圍內線性關繫良好(r=0.999 7,n=7),平均加樣迴收率為98.22%,RSD=2.62%(n=6).結論 本研究所建立的質量標準結果準確,靈敏度高,重複性良好,可用于複方沙塔榦口服液的質量控製.
목적 건립복방사탑간구복액적질량표준.방법 채용박층색보법대해제제중적군약천궁진행전속성감별;채용고효액상색보법대천궁중유효성분아위산진행함량측정.색보주:Diamonsil C18주(4.6 mm×250 mm, 5μm);류동상:갑순-1%빙작산,제도세탈(0~5 min,35%갑순;5~8 min,35%→23%갑순;8~22 min,23%갑순);검측파장:322 nm;류속:1.0 mL/min;주온:30 ℃;진양량:5μL.결과 아위산진양량재0.039 4~0.630 0μg범위내선성관계량호(r=0.999 7,n=7),평균가양회수솔위98.22%,RSD=2.62%(n=6).결론 본연구소건립적질량표준결과준학,령민도고,중복성량호,가용우복방사탑간구복액적질량공제.
Objective To establish the quality standards for compound Shatagan Oral Liquid. Methods Chuanxiong Rhizoma was identified by TLC. The content of ferulic acid was determined by HPLC. Separation was performed on a Diamonsil C18 column (4.6 mm × 250 mm, 5μm) with a mobile phase consisting of methanol-1% acetic acid solution in gradient elution (0-5 min, 35% methanol;5-8 min, 35%→23% methanol;8-22 min, 23% methanol) at 30℃;The flow rate was 1.0 mL/min;The injection volume was 5μL;The detection wavelength was 322 nm.Results Ferulic acid showed a good linear relationship in the range of 0.039 4-0.630 0μg (r=0.999 7,n=7). The average recovery was 98.22% and RSD was 2.62% (n=6).Conclusion The method is reliable, sensitive and with repeatability, which can be used as the quality control method for compound Shatagan Oral Liquid.