Identification of isoquercitrin metabolites produced by human intestinal bacteria using UPLC-Q-TOF/M

来源 :第十届全国药物和化学异物代谢学术会议暨第三届国际ISSX/CSSX联合学术会议 | 被引量 : 0次 | 上传用户:pz199
下载到本地 , 更方便阅读
声明 : 本文档内容版权归属内容提供方 , 如果您对本文有版权争议 , 可与客服联系进行内容授权或下架
论文部分内容阅读
  In this paper, ultra performance liquid chromatography/quadrupole time-of-flight mass spectrometry (UPLC-Q-TOF/MS) and the MetaboLynxTM software combined with mass defect filtering together were applied to identity the metabolites of isoquereitrin by the intestinal mixture bacteria and ninety six isolated strains from human feces.The human incubated samples collected 72 h in the anaerobic incubator and extracted with ethyl acetate were analyzed by UPLC-Q-TOF/MS within 10 min.A total of parent competent and 5 metabolites were identified by eight isolated strains including Bacillus sp.17, Veillonella sp.23, 32 and Bacteroides sp.40, 41,-56, 75, 88 in vitro.The results indicated that quercetin, acetylated isoquereitrin, dehydroxylated isoquercitrin, hydroxylated quercetin,hydroxymethylated quercetin were the major metabolites of isoquercitrin.Furthermore, a possible metabolism pathway on the biotransformation of isoquercitrin is established in intestinal flora.This study will be helpful for understanding the metabolic rout of isoquercitrin and the role of different intestinal bacteria on the metabolism of natural compounds.
其他文献
目的 泮托拉唑是一种质子泵抑制剂,临床上用于治疗消化道溃疡等疾病.由于其分子结构中有一手性硫原子,因此存在一对对映异构体.本文建立了用手性柱分离的色谱-串联质谱(LC-MS/MS)方法,可同时测定动物血浆中泮托拉唑两种对映体的浓度,可同时估算两者的药代动力学参数.用该方法分析了两种对映体在动物体内的构型转化.方法 比格犬和大鼠血浆用含内标左旋兰索拉唑的乙酸乙酯提取后,45℃条件下氮气挥干,经乙腈-
会议
氯高铁血红素因其化学性质较稳定,一直用于血红素铁吸收的研究中.但铁元素在各种基质中存在严重的背景干扰,给铁吸收研究带来很大的困难.本实验首先成功对氯高铁血红素进行58Fe稳定性标记.同时在使用CCT模式并采用数学公式对干扰进行校正的情况下,建立了快速、灵敏、专一的电感耦合等离子体质谱测定(ICP-MS)法.该方法样品处理简单,分析时间短,线性范围在0.005~1.0μg/mL.精密度和准确度均符合
Thymosin β4 (M.W.4976 Da; 44 amino acid peptide) has been investigated for the treatment of miocardial infarction.A bioanalytical assay based on ultra fast liquid chromatography coupled with electrosp
会议
细胞色素P450是哺乳动物的1相药物代谢酶,参与肝脏中内源及外源化合物代谢的单加氧酶,能够对大多数药物进行生物转化,是决定药物在人体内处置、安全性和有效性的关键酶。阐明药物对P450表达量的影响,对于预测临床上因药物相互作用而导致的毒性或减效作用是十分重要的,药物与P450的相互作用研究已成为创新药物能否进行人体试验的一个重要评价指标。以往在考察药物对酶的诱导或抑制时,仅根据P450酶总量或某几个
会议
Objective Alkyne hormones is a kind of synthetic steroids substances with low molecular weight, strong lipophilicity and good biological activites, which play an important role in the regulation of hu
目的 建立一种创新的正负谱实时切换的LC-MS/MS法同时测定血浆中黄连解毒汤13种主要活性成分,进而对其在大鼠体内的药代动力学行为进行评价.方法 色谱柱为SB-C18柱(4.6 mm×150 mm,5μm粒径),流动相为甲醇及0.1%甲酸,梯度洗脱,柱温40℃,总分析时间为6 min.检测器选择Qtrap5500三重串联四极杆质谱仪,配有电喷雾离子源,应用实时正负谱切换模式.其中小檗碱、巴马汀、
Objective This study is an investigation of the anti-inebriation effects of a herbal composition of Semen Hoveniae, Radix Puerariae and Fructus Schisandrae (SRF) against acute alcoholic intoxication.M
会议
目的 建立生物样本中同时测定9种人参皂苷中主要的皂苷类化合物Rb1,Rb2/Rb3,Rc,Rd,Re,Rf, Rhl和gg1的LC-ESI-MS方法,并应用于各组分的药代动力学研究中.方法 生物样本采用正丁醇液-液萃取,经C18柱梯度洗脱程序进行色谱分离(流速为0.2 mL/min),采用电喷雾(ESI)离子源以负离子方式检测.大鼠灌胃(ig) 200 mg/kg人参总皂苷,尾静脉注射(iv) 1
会议
目的 探讨槲皮素在人肠道吸收模型Caco-2细胞单层上的吸收和代谢特征.方法 LC-MS法测定槲皮素、异鼠李亭和柽柳黄素,采用Caco-2单层细胞模型研究槲皮素的肠道吸收及代谢特征.结果 150 min孵育时间内,均能在透过侧检测到槲皮素,呈现浓度和时间依赖性(P< 0.05);B→A的透过量是A→B的2.2倍;透过面槲皮素在150 min孵育时间内呈先升后降的动态趋势特征,120 min达峰,随
Guanxin-danshen decoction (GDD, including Radix Salviae Miltiorrhiae, Radix Notoginsen, and Lignum Dalbergiae Odoriferae), the classic TCM prescription, has been with systematic pharmacodynamic studie
会议