Zhang Zhenzhen, Xie Tao, Liu Houru, Yang Ting, Sun Yue, Wei Xiyu, Xu Wenwu, Yu Peihua, Yu Dehong, Li Wei
North China University of Science and Technology, Hebei, Tangshan 063210, PR China.
Canada Royal Enoch Phytomedicine Ltd, Vancouver V6S 2L9, Canada.
J Chromatogr B Analyt Technol Biomed Life Sci. 2022 Jan 15;1189:123039. doi: 10.1016/j.jchromb.2021.123039. Epub 2021 Nov 23.
Dammar-20(22)E,24-Diene-3β,6α,12β-Triol (YNPT2), as one of the main pharmacological and active components of Panax ginseng, promotes ubiquitination and degradation of hypoxia inducible factor Ia through proteasome, which reduces the content of hypoxia inducible factor Ia in tumor cells. Therefore, it is widely used in tumor inhibition. A sensitive and specific bioanalytical method of liquid chromatography-tandem mass spectrometry (LC-MS/MS) for the quantification of YNPT2 rat plasma has been developed. Buspirone was used as the internal standard (IS). A 50 μl aliquot of rat plasma sample was deproteinized by 150 μl methanol-acetonitrile (1:1,v:v), vortex-mixed for 1 min and centrifuged at 15,000 r/min for 10 min at 4 °C. Then, 120 μl of supernatant was pipetted out into the autosampler vials and analyzed by LC-MS/MS with 10 μl injection volume. Chromatographic separation was performed on an Agilent ZORBAX XDB-C column (2.1 × 50 mm, 3.5 µm) with mobile phases consisting of water containing 5 mM ammonium acetate (mobile phase A) and acetonitrile (mobile phase B) at a flow rate of 0.6 ml/min over a total run time of 4.0 min. YNPT2 and buspirone (IS) were detected and quantified using positive electrospray ionization in multiple reaction monitoring (MRM) mode with transitions of m/z 441.4 → 109.1 for YNPT2 and m/z 386.3 → 122.1 for IS. The linear range was 5-2000 ng/ml with the square regression coefficient (r) of 0.9972, and the lower limit of quantification (LLOQ) was 5 ng/ml. The intra-day and inter-day precision deviations of YNPT2 ranged from 3.8 to 6.9% and 3.5-5.8%, and accuracy error ranged from -7.4-5.9% and -9.2-11.9%. The average extraction recovery of YNPT2 in rat plasma was between the range of 98.5%-102.7%. This method was successfully applied to study the pharmacokinetics of YNPT2 in rats after intragastric administration at a single dose of 10.0 mg/kg and after intravenous injection at a single dose of 2.0 mg/kg.
达玛-20(22)E,24-二烯-3β,6α,12β-三醇(YNPT2)作为人参的主要药理活性成分之一,通过蛋白酶体促进缺氧诱导因子Ia的泛素化和降解,从而降低肿瘤细胞中缺氧诱导因子Ia的含量。因此,它被广泛用于肿瘤抑制。已开发出一种灵敏且特异的液相色谱-串联质谱(LC-MS/MS)生物分析方法,用于定量大鼠血浆中的YNPT2。丁螺环酮用作内标(IS)。取50 μl大鼠血浆样品,加入150 μl甲醇-乙腈(1:1,v:v)进行蛋白沉淀,涡旋混合1分钟,然后在4℃下以15,000 r/min离心10分钟。接着,吸取120 μl上清液放入自动进样瓶中,以10 μl进样体积通过LC-MS/MS进行分析。色谱分离在安捷伦ZORBAX XDB-C柱(2.1×50 mm,3.5 µm)上进行,流动相由含5 mM醋酸铵的水(流动相A)和乙腈(流动相B)组成,流速为0.6 ml/min,总运行时间为4.0分钟。使用正电喷雾电离在多反应监测(MRM)模式下检测和定量YNPT2和丁螺环酮(内标),YNPT2的质荷比跃迁为m/z 441.4→109.1,内标的质荷比跃迁为m/z 386.3→122.1。线性范围为5 - 2000 ng/ml,平方回归系数(r)为0.9972,定量下限(LLOQ)为5 ng/ml。YNPT2的日内和日间精密度偏差范围分别为3.8%至6.9%和3.5%至5.8%,准确度误差范围分别为-7.4%至5.9%和-9.2%至11.9%。YNPT2在大鼠血浆中的平均提取回收率在98.5% - 102.7%之间。该方法成功应用于研究YNPT2在大鼠单次口服10.0 mg/kg和单次静脉注射2.0 mg/kg后的药代动力学。