Objective To establish an HPLC method for the determination of oxysophocarpin in rat plasma, and study the pharmacokinetics of oxysophocarpin in Kuqi drop pills. Methods The analytical column was Inertsil-NH2 (150 mm × 4. 6 mm,5 μm); mobile phase:acetonitrile-ethanol-3% phosphoric acid water (86∶8∶6);flow rate:1. 0 mL/min; detection wavelength: 220 nm; injection volume: 20 μL. Results The linear concentration range of plasma oxysophocarpin was 0. 20~20 μg/mL,r=0. 993,the lower limits of quantificati were 0. 20 μg/mL. The intra-day and inter-day precision,accuracy,extraction recoveries met the requirement. Six rats were fed by gavage administra-tion of 8. 5 mg/kg Kuqi drop pills,the plasma oxysophocarpin Tmax was (4. 03 ± 0. 72)h,Cmax was (4. 00 ± 0. 54)ng/mL,t1/2 was ( 0. 053 ± 0. 66 ) h, AUC0-t was ( 30. 70 ± 0. 54 ) μg·h/mL, AUC0-∞ was ( 30. 8 ± 0. 32 ) ng·h/mL. Conclusion The method is simple,rapid,accurate,specific,it can be used for the pharmacokinetic study of oxyso-phocarpin in Kuqi drop pills.%目的:建立测定血浆中氧化槐果碱浓度的高效液相色谱法,并用此方法进行苦芪滴丸中氧化槐果碱的药代动力学研究。方法色谱柱为Inertsil-NH2(150 mm ×4.6 mm,5μm);流动相:乙腈-无水乙醇-3%磷酸水(86∶8∶6);流速:1.0 mL/min;检测波长:220 nm;进样量:20μL。结果血浆中氧化槐果碱的线性范围:0.20~20μg/mL,r=0.993,最低检测限为0.20μg/mL。日内、日间精密度及准确度、提取回收率符合要求。6只大鼠灌胃给药8.5 mg/kg苦芪滴丸后,血浆中氧化槐果碱Tmax为(4.03±0.72)h,Cmax为(4.00±0.54)ng/mL, t1/2为(0.05±0.66)h,采用梯形法计算,AUC0-t为(30.70±0.54)μg·h/mL,AUC0-∞为(30.8±0.32)ng·h/mL。结论本方法简便、快速、准确、专属性强,可用于苦芪滴丸中氧化槐果碱的药代动力学研究。
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