目的 建立HPLC波長切換法同時測定腎炎靈膠囊中柳穿魚葉苷、地榆皂苷-Ⅰ、女貞苷、特女貞苷、去甲蟛蜞菊內(nèi)酯和蟛蜞菊內(nèi)酯。方法 采用高效液相色譜法，Agilent Extend-C₁₈色譜柱（250 mm×4.6 mm，5 μm）；流動相：甲醇-乙腈（1：1）與0.5%冰醋酸溶液，梯度洗脫；檢測波長：330 nm（0~14 min檢測遠柳穿魚葉苷）、203 nm（14~20 min檢測地榆皂苷-Ⅰ）、224 nm（20~29 min檢測女貞苷和特女貞苷）、351 nm（29~45 min檢測去甲蟛蜞菊內(nèi)酯和蟛蜞菊內(nèi)酯）；體積流量：0.8 mL/min；柱溫：30℃；進樣量為10 μL。結(jié)果 柳穿魚葉苷、地榆皂苷-Ⅰ、女貞苷、特女貞苷、去甲蟛蜞菊內(nèi)酯和蟛蜞菊內(nèi)酯分別在2.97~59.40、19.59~391.80、1.78~35.60、4.96~99.20、1.13~22.60、3.29~65.80 μg/mL線性關(guān)系良好；平均回收率分別為97.97%、99.78%、96.98%、98.52%、98.10%、99.10%，RSD值分別為0.76%、1.01%、0.66%、1.22%、0.95%、1.56%。結(jié)論 該方法簡便，分析速度快，為完善腎炎靈膠囊的質(zhì)量標準提供參考。

Objective To develop an HPLC wavelength switching method for simultaneous determination of pectolinarin, ziyu-glycoside I, ligustroflavone, specnuezhenide, demethylwedelolactone, and wedelolactone, in Shenyanling Capsules. Methods HPLC method was adopted for the analysis on Agilent Extend-C₁₈ column (250 mm×4.6 mm, 5 μm). The mobile phase consisted of methanol-acetonitrile (1:1) and 0.5% glacial acetic acid solution with gradient elution. The detection wavelengths were 330 nm in 0-14 min (determination of pectolinarin), 203 nm in 14-20 min (determination of ziyu-glycoside I), 224 nm in 20-29 min (determination of ligustroflavone and specnuezhenide), and 351 nm in 29-45 min (determination of demethylwedelolactone and wedelolactone).The flow rate was 0.8 mL/min, and the column temperature was set at 30℃ with injection volume of 10 μL. Results Pectolinarin, ziyu-glycoside I, ligustroflavone, specnuezhenide, demethylwedelolactone and wedelolactone had good linearity in the ranges of 2.97-59.40, 19.59-391.80, 1.78-35.60, 4.96-99.20, 1.13-22.60, and 3.29-65.80 μg/mL, respectively. The average recoveries were 97.97%, 99.78%, 96.98%, 98.52%, 98.10%, and 99.10%, with RSD of 0.76%, 1.01%, 0.66%, 1.22%, 0.95%, and 1.56%, respectively. Conclusions The method is simple and rapid which provides reference for quality standard of Shenyanling Capsules.