目的:利用RP—HPLC—ELSD技术建立不同产地茯苓三萜的指纹图谱,为评价不同产地的茯苓药材的质量品质提供理论依据。方法:色谱柱为Kromasil100—5C18柱(4.6mm×250mm,5μm),流动相0.2%甲酸水溶液(A)-乙腈(B),采用梯度洗脱法,流速1.0mL·min^-1,柱温30℃,蒸发光检测条件:雾化温度40℃,压力350kPa,gain值为7;进样量20μL。结果:建立的指纹图谱中有18个共有峰,方法学考查表明,各主要色谱峰相对保留时间及峰面积的RSD均〈3%,峰面积占总峰面积〉10%的共有峰其相对峰面积差值均在±25%以内,符合指数图谱的技术要求,仪器的精密度良好,且供试品溶液至少12h内稳定。结论:该方法简便快速、准确可靠,可作为评价不同产地茯苓药材质量的有效手段。
Objective: Investigation on RP-HPLC-ELSD fingerprint of triterpenes in Poria cocos from different origin place, in order to provide a theory evidence to evaluate the quality of P. cocos from different origin place, and improve the quality of P. cocos. Method: The chromatographic conditions were Kromasil 100-5 C18 column (4.6 mmx 250 mm, 5μm), 0.2% methanoic acid (A) and acetonitrile (B) as gradient mobile phases, flow rate being 1.0 mL .min-1, column temperature at 30 ℃ , evaporative light-detection conditions: atomization temperature at 40 ℃, pressure of 350 kPa, gain value of 7, and 20 μL sample injection. Result: Fingerprint was established with 18 common peaks and methodology reached the required standard. Conclusion: The method is simple, rapid, accurate, and can be used as an effective means of P. cocos quality evaluation of different origin place.