摘要
目的:建立道地药材黔党参的指纹图谱研究方法,为其质量控制提供理论依据。方法:采用高效液相色谱法。色谱柱为依利特-C18(250mm×4.6mm,5μm),流动相为乙腈-0.2%冰醋酸水溶液(梯度洗脱),流速为0.8ml/min,柱温为30℃,检测波长为270nm。结果:所测10批黔党参样品有13个共有峰,共有峰峰面积的RSD为49.67%~100.93%,峰面积比值的RSD为40.86%~127.97%;共有峰相对保留时间为0.441~1.675,相对保留时间的RSD为0.11%~1.50%;该方法具有良好的稳定性和重复性。结论:所建黔党参HPLC指纹图谱分析方法可较全面地反映该药材中化学成分的信息,可为该药材的质量控制提供理论依据。
OBJECTIVE: To establish the method for fingerprint study of genuine regional drug Codonopsis tubulosa in Gui- zhou. METHODS: HPLC method was adopted. The separation was performed on Hypersil C18(250 mm×4.6 mm, 5 μm)column with mobile phase consisted of acetonitrile-0.2% glacial acetic acid aqueous solution (gradient elution) at the flow rate of 0.8 ml/ min. The column temperature was 30 ℃ and UV detection wavelength was set at 270 nm. RESULTS: There were 13 common peaks of 10 batches of C. tubulosa samples. The RSD of common peak area was from 49.67% to 100.93%. The RSD of relative peak area was from 40.86% to 127.97%. The relative retention time of common peak was 0.441-1.675. The RSD of relative reten- tion time was from 0.11% to 1.50%. The method is of good stability and repeatability. CONCLUSION: Established HPLC chro- matographic fingerprints of C. tubulosa could express its chemical information, and provide a basis for quality control of C tubulo-sa.
出处
《中国药房》
CAS
CSCD
2013年第7期628-630,共3页
China Pharmacy
基金
贵阳市科学技术计划项目资助(筑科合同〔2011207〕22号
〔2010〕筑科农合同字第1-中-14号)
贵阳中医学院科研项目资助(贵中医科院内〔2010〕09)