目的研究甘草酸对芍药苷大鼠肠吸收的影响。
ObjectiveTo study the effects of glycyrrhizin on intestinal absorption of paeoniflorin by the everted rat gut sac model.
方法采用大鼠在体肠灌流方法，研究卡马西平大鼠肠吸收动力学。
Methods The absorption kinetics and absorption sites were investigated by using in situ perfusion method in rats.
目的：考察丹参素在大鼠各肠段的吸收动力学特征及不同药物浓度对其的影响。
OBJECTIVE: To investigate the absorption kinetics of danshensu at different intestine segments in rats and the influence of the drug concentration on the absorption kinetics.
目的：探讨川芎嗪在大鼠各肠段的吸收动力学特征。
OBJECTIVE To investigate the absorption kinetics of ligustrazine at different intestine segments in rats.
目的研究阿魏酸在大鼠各肠各段的吸收动力学特征。
Objective To investigate the absorption kinetics of ferulic acid at different intestine segments in rats.
目的研究尼群地平在大鼠各肠段的吸收动力学特征。
OBJECTIVE To investigate the absorption kinetics of nitrendipine at different intestine segments in rats.
目的研究泛昔洛韦在大鼠各肠段中的吸收动力学特征。
Aim To investigate the absorption kinetics of famciclovir at different intestine segments in rats.
方法：采用大鼠在体肠循环模型和高效液相色谱法研究白术内酯Ⅰ在大鼠各肠段的吸收特性。
Method: The absorption kinetics was investigated using the method of in situ intestine absorption in rats and the samples were determined by HPLC.
用二房室模型比较了原位灌流的大鼠空肠和迴肠锌吸收速率常数及动态过程。
The kinetics of zinc absorption of jejunum and that of ileum were compared in perfused rats by a two-compartmental model.
目的：编制大鼠在体肠吸收实验数据处理程序。
Objective: To compile the program for data analysis in test of intestinal absorption in rats.
采用大鼠在体肠灌流法，比较续断总皂苷及其磷脂复合物的在体肠吸收情况。
Rat intestine perfusion was use to compare aspersaponin absorption under with and without phospholipid.
采用单向灌流技术考察长春西汀的大鼠在体肠吸收性质。
The in situ intestinal absorption property of vinpocetine in rats was investigated by means of single-pass intestinal perfusion technique.
目的考察依托度酸在大鼠各肠段的吸收动力学特征。
Objective to investigate the in situ intestinal absorption kinetics of etodolac in rats.
目的研究莪术油中三成分对大鼠在体肠的吸收情况。
Aim To study the absorption of zedoary oil in intestine of rat.
目的研究磷酸川芎嗪的大鼠在体肠吸收性质。
Objective To investigate the absorption characteristic of tetramethylpyrazine phosphate (TMPP) in various intestinal segments.
方法采用大鼠在体肠灌流吸收实验，研究了氧化苦参碱的吸收部位和吸收动力学特征。
METHODS: The absorption kinetics and absorption site of oxymatrine were investigated using in situ perfusion method in rats.
目的分别考察芍药苷在大鼠各肠段的吸收动力学特征及不同药物浓度对其的影响。
OBJECTIVE To investigate the absorption kinetics of paeoniflorin at different intestine segments of rats and the influence of the drug solution concentration on the absorption kinetics.
结果芍药苷在大鼠十二指肠、空肠、回肠和结肠均有吸收，甘草酸几乎抑制芍药苷在各个肠段的吸收。
ResultsPaeoniflorin could be absorbed in duodenum, jejunum, ileum and colon of rats, and glycyrrhizin could inhibit the absorption of paeoniflorin.
目的研究利巴韦林在大鼠各肠段的吸收动力学特征。
Objective To determine the absorption characters of ribavirin from various intestinal segments.
方法：采用大鼠在体肠灌流模型对淫羊藿苷在大鼠各肠段的吸收特性进行研究。
Methods: to establish the situ intestinal perfusion model and to study the absorption of icariin for various intestinal segments.
方法采用大鼠在体肠吸收实验方法，用HPLC对循环液中的芍药苷进行分析。
METHOD The intestine in rats was cannulated for in situ recirculation. Paeoniflorin concentration in the flux was measured by the reversed phase HPLC.
方法：以大鼠在体肠灌流模型从吸收部位、药物浓度考察秦皮甲素的肠吸收动力学情况。
Method: the study was performed by intestinal perfusion model in rats to observe the effect of absorption sites and concentrations on absorption kinetics of aesculin.
方法采用大鼠在体肠循环法分别研究盐酸去氢骆驼蓬碱在大鼠十二指肠、空肠、回肠及结肠中的吸收动力学特征。
Method the absorption kinetics of harmine hydrochloride from duodenum, jejunum, ileum, and colon were investigated using in situ perfusion method in the rats.
方法采用大鼠在体小肠循环法和离体外翻肠囊法研究灯盏花素普通粉剂和灯盏花素磷脂复合物的小肠吸收及肠壁通透性。
The everted gut sac experiment was used to study the absorption rate on the ex vivo small intestine of broiler chickens.
目的研究淫羊藿中黄酮类化合物在大鼠各肠段的吸收动力学特征。
OBJECTIVE to investigate the absorption characteristics and mechanism of the total flavones of epimedium for various intestinal segments.
方法采用大鼠在体肠吸收模型，以高效液相色谱法测定循环液中药物的浓度。
METHODS the model of in situ intestinal perfusion was used. A HPLC method was established to determine the drug concentration in the perfusate.
方法采用大鼠在体肠吸收模型，以高效液相色谱法测定循环液中药物的浓度。
METHODS the model of in situ intestinal perfusion was used. A HPLC method was established to determine the drug concentration in the perfusate.
应用推荐