葛根芩连汤中14种主要成分在大鼠体内的药动学特征研究Pharmacokinetic characteristics of fourteen main components of Gegen Qinlian Decoction in rats
王新雨,晋臻,凌霄,刘昌顺,谭晓梅
WANG Xin-yu,JIN Zhen,LING Xiao,LIU Chang-shun,TAN Xiao-mei
摘要(Abstract):
该研究采用超高效液相色谱-串联质谱(UPLC-MS/MS)方法,研究大鼠单次灌胃葛根芩连汤(15 mL·kg~(-1))后血浆中葛根素、3′-羟基葛根素、大豆苷、大豆苷元、染料木苷、染料木素、黄芩苷、黄芩素、汉黄芩苷、汉黄芩素、小檗碱、药根碱、巴马汀、甘草苷14种主要成分的药动学特征。采用Zorbax SB-18色谱柱以乙腈(A)-0.1%甲酸水溶液(B)为流动相对分析物和内标(柚皮苷和泼尼松龙)进行梯度洗脱:0~2.5 min,15%~30%A;2.5~3.5 min,30%~35%A;3.5~5.0 min,35%~40%A;5.0~9.0 min,40%~60%A;9.0~11.0 min,60%~15%A。流速为0.4 mL·min~(-1)。采用电喷雾电离(ESI)源以多反应监测(MRM)模式进行正负离子检测。结果14种成分的线性相关系数大于0.99,血浆样品反复冻融3次、-20℃放置7 d、室温放置12 h以及血浆样品处理后放置24 h的日内、日间变异系数(RSD)小于10%,精密度和准确度等均符合生物样品分析的要求。表明该方法灵敏、准确,适用于葛根芩连汤中14种成分的药动学研究。采用DAS 3.2.2软件的非房室模型计算药动学参数,结果异黄酮类成分和黄酮类成分的MRT_(0-)_t在7.5~11.8,T_(1/2z)主要在11.0~29.7 h,黄酮类AUC_(0-)_t大于异黄酮类。而生物碱类成分的MRT_(0-)_t在4.3~7.2 h,T_(1/2z)在1.0~5.0 h,AUC_(0-)_t小于黄酮类和异黄酮类成分。结果提示黄酮及异黄酮类成分体内血药浓度高、作用时间长,有利于抗炎解热作用的发挥;生物碱类成分体内血药浓度低,作用时间短,可能在肠道内发挥其抑菌作用。
A specific and selective UPLC-MS/MS method was developed and validated for the simultaneous determination of isoflavonoids(3′-hydroxy puerarin, puerarin, daidzin, daidzein, genistin, genistein), flavonoids(baicalin, baicalein, wogonoside, wogonin, liquiritin)and alkaloids(berberine, jatrorrhizine, palmatine)(14 bioactive compounds) of Gegen Qinlian Decoction(GQD)in plasma. The pharmacokinetics characteristics of 14 bioactive compounds were study after oral administration of GQD at a single dose to rats. Prednisolone was used as the internal standard of liquiritin, and naringin was used as the internal standard of the other thirteen analytes. After the plasma samples were processed by precipitation protein method, the constituents and internal standards were gradient eluted by using a Zorbax SB-18 column with a mobile phase of acetonitrile(A) and 0.1% formic acid aqueous solution(B) using a gradient elution of 0-2.5 min,15%-30% A;2.5-3.5 min,30%-35% A;3.5-5.0 min,35%-40% A;5.0-9.0 min,40%-60% A;9.0-11.0 min,60%-15% A,and the flow rate was 0.4 mL·min~(-1). The auto sampler was conditioned at 25 ℃ and the sample injection volume was 5 μL. A mass spectrometry was applied with electrospray ionization(ESI) ion source in the positive and negative ion multiple reaction monitoring(MRM) mode. All pharmacokinetic parameters were processed by non-compartmental analysis with DAS 3.2.2 software. The results showed that the linear correlation coefficient of the 14 components were all greater than 0.99, indicating that the method had good linearity in their respective concentration ranges. Post-preparative stability(25 ℃, 24 h), short-term stability(25 ℃, 12 h), long-term stability(-20 ℃, 7 d), and freeze and thaw stability(3-cycles) of the fourteen constituents were examined to evaluate the stability of methodology. The results of the inner and inter-day relative standard deviations were both less than 10%, indicating legitimate precise and accuracy to the requirement of biological sample analysis. The assay method is proved to be sensitive,accurate and convenient. It can be applied to the pharmacokinetic study of the fourteen analytes. The kinetic parameters of the related drugs were calculated according to the blood concentration of the 14 components. The results showed that the MRT_(0-)_t of the isoflavones and flavonoids was 7.5-11.8 h, T_(1/2 z )were mainly in 11.0-29.7 h, and the AUC_(0-)_t flavonoids were larger than the isoflavones. The MRT_(0-)_t of alkaloids were between 4.3-7.2 h, T_(1/2 z) were 1.0-5.0 h, AUC_(0-)_t were less than flavonoids and isoflavones. The results suggest that flavonoids and isoflavones have a high concentration of blood and long time of action, which are beneficial to the anti-inflammatory and antipyretic effects. The concentration of alkaloids in the body is low and the time of action is short, and it may play its bacteriostasis in the intestinal tract.
关键词(KeyWords):
葛根芩连汤;超高效液相色谱-串联质谱;药代动力学
Gegen Qinlian Decoction;UPLC-MS/MS;pharmacokinetics
基金项目(Foundation): 国家自然科学基金项目(81374049)
作者(Author):
王新雨,晋臻,凌霄,刘昌顺,谭晓梅
WANG Xin-yu,JIN Zhen,LING Xiao,LIU Chang-shun,TAN Xiao-mei
参考文献(References):
- [1] 郝瑞丽. 葛根芩连汤合平胃散加味治疗急性胃肠炎临床观察[J]. 实用中医药杂志, 2018, 34(7): 765.
- [2] 杨红, 张莉. 加味葛根芩连汤联合醒脾养儿颗粒治疗小儿轮状病毒性肠炎的临床疗效及其对患儿心肌酶谱的影响[J]. 临床合理用药杂志, 2018, 11(21): 83.
- [3] 白金钟. 葛根芩连汤饮片治疗2型糖尿病的临床疗效观察[J]. 世界最新医学信息文摘, 2018, 18(84): 140.
- [4] 涂珺, 朱水兰, 周小妹. 黄芩苷、小檗碱和葛根素体外胰岛素抵抗细胞差异化降糖作用研究[J].中国中药杂志, 2018, 43(20):
- [5] 杜晨晖, 李津, 闫艳, 等. 葛根芩连汤及其发酵产物干预2型糖尿病大鼠的1H-NMR代谢组学研究[J]. 中草药, 2018,49(10):2302.
- [6] 张启云. 色谱-质谱联用技术分析方法和葛根芩连汤疗效机制及代谢组学研究[D].武汉:武汉大学,2016.
- [7] Ling X, Xiang Y Q, Tang Q F, et al. Comparative pharmacokinetics of eight major bioactive components in normal and bacterial diarrhea mini-pigs after oral administration of Gegen Qinlian Decoction[J]. J Chromatogr B, 2017(1044/1045): 132.
- [8] Wang Q, Song W, Qiao X, et al. Simultaneous quantification of 50 bioactive compounds of the traditional Chinese medicine formula Gegen Qinlian Decoction using ultra-high performance liquid chromatography coupled with tandem mass spectrometry[J]. J Chromatogr A, 2016, 1454: 15.
- [9] 王小康, 刘清霞, 叶开和, 等.3′-羟基葛根素对脂肪细胞3T3-L1胰岛素抵抗的影响及其机制研究[J]. 中草药, 2014, 45(16): 2352.
- [10] 张泉洋, 马富超, 王帅, 等. 染料木苷药理作用的研究进展[J]. 国际药学研究杂志, 2017,44(4):315.
- [11] 翁春艳, 杨艳, 李晓波. 染料木素抗动脉粥样硬化的研究进展[J]. 中国医药指南, 2016, 14(7): 33.
- [12] 蔡标, 叶树, 王艳, 等. 染料木素对Aβ25-35诱导PC12细胞损伤的保护作用及CaM-CaMKIV信号通路的影响[J]. 中国中药杂志, 2018,43(3):571.
- [13] 梅建凤, 刘姜华, 易喻, 等. 染料木素与其糖苷的抗肿瘤和抗氧化活性比较[J]. 中国药理学通报, 2017,33(8):1182.
- [14] 谭晓梅, 吴艳萍. 葛根芩连汤配伍葛根素在兔体内药动学的研究[J]. 中药药理与临床, 2006, 22(5): 1.
- [15] 黄晓巍, 张丹丹, 王晋冀, 等. 葛根化学成分及药理作用[J]. 吉林中医药, 2018, 38(1):87.
- [16] 包永睿, 王帅, 杨欣欣, 等. 葛根异黄酮类成分对缺氧复氧损伤心肌细胞保护作用的研究[J]. 中成药, 2015, 37(7): 1514.
- [17] 韩美玉, 韩志远. 甘草酸二铵佐治支气管哮喘对肺功能、气道炎症和免疫功能的影响[J]. 中国药业, 2018,27(18):56.
- [18] 恽菲, 康安, 狄留庆, 等. 甘草酸配伍蛇床子素对大鼠酒精性脂肪肝的治疗作用[J]. 南京中医药大学学报, 2018,34(5):504.
- [19] Takeda S, Ishihara K, Wakui Y. Bioavailability study of glycyrrhetic acid after oral administration of glycyrrhizin in rats; relevance to the intestinal bacterial hydrolysis[J]. J Pharm Pharmacol, 1996, 48: 902.
- [20] 王文玉, 戴建业, 孙淑军, 等. 黄芩素药代动力学研究进展[J]. 世界科学技术——中医药现代化, 2011, 13(6): 1018.
- [21] 周红潮, 杜锐, 王慧, 等. 黄芩苷药代动力学研究进展[J]. 中国中药杂志, 2018, 43(4):684.
- [22] 夏笔军. 汉黄芩苷和汉黄芩素肠局部循环新处置机制[D]. 广州:南方医科大学, 2010.
- [23] Dai P M, Zhu L J, Luo F F, et al. Triple recycling processes impact systemic and local bioavailability of orally administered flavonoids[J]. AAPS J, 2015, 17(3): 723.
- [24] 沈安, 吴璐, 朱卫丰. 黄芩中黄芩苷与黄芩素的体内外转化研究进展[J]. 江西中医药, 2017,48(9):71.
- [25] Lu T, Song J, Huang F, et al. Comparative pharmacokinetics of baicalin after oral administration of pure baicalin, Radix Scutellariae extract and Huanglian Jiedu Tang to rats[J]. J Ethnopharmacol, 2007, 110(3):412.
- [26] 闫晶超, 刘兆明, 王天明, 等. 泻心汤黄酮类成分在大鼠体内的药代动力学研究[J]. 药学学报, 2007, 42(7): 722.
- [27] 李见春. 汉黄芩素吸收及代谢机制的研究[D]. 合肥:安徽医科大学,2010.
- [28] 郑京玉,李国峰,何忠梅,等. 黄藤中巴马汀与药根碱在大鼠体内药动学及口服生物利用度的研究[J]. 中国中药杂志, 2017,42(14):2773.
- [29] 朱容慧, 赵军宁, 毕岳琦, 等. 中药肠吸收动力学的研究进展[J]. 药物评价研究, 2010, 33(1): 25.
- [30] Simons A L, Renouf M, Suzanne Hendrich A, et al. Human gut microbial degradation of flavonoids: structure-function relationships[J]. J Agric Food Chem, 2005, 53(10): 4258.
- [31] 彭游, 邓泽元. 新型大豆苷元衍生物的前体药物判定及其在大鼠体内药物动力学的研究[J]. 时珍国医国药, 2011, 22(9): 2156.
- [32] 王本杰, 袁桂艳, 刘焕君, 等. HPLC测定血浆中黄豆苷元浓度及其人体药动学研究[J]. 中国药学杂志, 2007, 42(18): 1422.