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HPLC-UVD法测定肿节风水提物及相关制剂中迷迭香酸及异嗪皮啶的含量
引用本文:潘宇明,姚志红;戴 毅;张 依;段营辉;姚新生. HPLC-UVD法测定肿节风水提物及相关制剂中迷迭香酸及异嗪皮啶的含量[J]. 沈阳药科大学学报, 2010, 27(6): 457-462
作者姓名:潘宇明  姚志红;戴 毅;张 依;段营辉;姚新生
作者单位:(1. 暨南大学 中药及天然药物研究所,广东 广州 510632; 2. 中药药效物质基础及创新药物研究广东省高校重点实验室,广东 广州 510632;3. 沈阳药科大学 中药学院,辽宁 沈阳 110016)
摘    要:目的采用HPLC法测定肿节风水提取物及相关制剂中迷迭香酸和异嗪皮啶的含量,为肿节风提取物及制剂的质控方法奠定基础。方法采用C18色谱柱(250 mm×4.6 mm,5μm),以乙腈-水(分别含体积分数为0.1%甲酸)为流动相梯度洗脱,流速1.00 mL.min-1,检测波长330 nm,柱温35℃。结果迷迭香酸的质量浓度在4.746~189.8 mg.L-1内、异嗪皮啶的质量浓度在1.018~40.72 mg.L-1内线性关系良好;仪器精密度试验、重复性试验、稳定性试验RSD均不大于2.0%。肿节风水提取物中迷迭香酸与异嗪皮啶的回收率分别为99.8%和99.2%,RSD分别为0.70%和0.63%(n=6);迷迭香酸与异嗪皮啶在相关制剂中回收率分别为100.7%和98.4%,RSD分别为1.6%和0.44%(n=6)。12批肿节风水提取物供试品中迷迭香酸的含量在1.479~6.447 mg.g-1内、异嗪皮啶的含量在1.912~3.540 mg.g-1内;在以肿节风水提取物制成的相关制剂中,迷迭香酸的含量在0.847~15.946 mg.g-1内、异嗪皮啶的含量在2.032~4.093 mg.g-1内。结论作者建立的肿节风及制剂的定量分析方法简便、快速、专属性强、重现性好,为肿节风水提取物及相关制剂质量标准的提升奠定了基础。

关 键 词:肿节风  迷迭香酸  异嗪皮啶  含量测定  抗炎活性成分  高效液相色谱-紫外检测法
收稿时间:2009-10-15
修稿时间:2010-01-15

Content determination of rosmarinic acid and isofraxidin in Sarcandra glabra extract and preparations by HPLC-UVD
PAN Yu-ming,YAO Zhi-hong,DAI Yi,ZHANG Yi,DUAN Ying-hui,YAO Xin-sheng. Content determination of rosmarinic acid and isofraxidin in Sarcandra glabra extract and preparations by HPLC-UVD[J]. Journal of Shenyang Pharmaceutical University, 2010, 27(6): 457-462
Authors:PAN Yu-ming  YAO Zhi-hong  DAI Yi  ZHANG Yi  DUAN Ying-hui  YAO Xin-sheng
Affiliation:(1. Institute of Traditional Chinese Medicine & Natural Products, Jinan University, Guangzhou 510632, China; 2. Guangdong Provice Key Laboratory of Pharmacodynamic Constituents of TCM and New Drug Research, Guangzhou 510632, China; 3. School of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University, Shenyang 110016, China)
Abstract:Objective To develop an HPLC-UVD method for content assay of rosmarinic acid and isofraxidin in Sarcandra glabra extract and preparations. Method The method was developed on an C18 column (250 mm× 4.6 mm, 5 μm) by gradient elution with acetonitrile-water (both containing 0.1% formic acid) as mobile phase at a flow rate of 1.00 mL·min-1 with the wavelength at 330 nm and column temperature at 35 ℃. Results The linearity was good over the range of 4.746-189.8 mg·L-1 for rosmarinic acid and 1.018-40.72 mg·L-1 for isofraxidin. The RSD was no more than 2.0% in precision test, reproducibility test and stability test, respectively. The average recovery of rosmarinic acid and isofraxidin in Sarcandra glabra extract were 99.8% (RSD=0.70%) and 99.2% (RSD=0.63%), while in preparations were 100.7% (RSD=1.6%) and 98.4% (RSD=0.44%), respectively. The twelve batches of Sarcandra glabra extract sample shared an average content over the range of 1.479-6.447 mg·g-1 for rosmarinic acid and 1.912-3.540 mg·g-1 for isofraxidin, while 0.847-15.946 mg·g-1 for rosmarinic acid and 2.032-4.093 mg·g-1 for isofraxidin in preparations. Conclusion The method is simple, specific, precise and accurate and can help to improve the quality standard of Herba Sarcandrae extract and preparation.
Keywords:Herba Sarcandrae rosmarinic acid  isofraxidin  content determination  anti-inflammatory activity component  HPLC-UVD`
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