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All rats except normal control group were made up bizheng animal model, and administered ra decocted liquids for 30 days.

模型对照组和各给药组于复制痹证动物模型后,按组给药30 d。

You know the fact that the majority of the drugs and dosing, we talked about daily dosing of different drugs.

我们知道大多数药物的给药剂量,探讨了不同的药物的日给药剂量。

Methods The experiments adopted eternalized human hepatic stellate cell (HSC-T6) builded model by acetaldehyde,for study in vitro.

方法采用乙醛造模后的肝星状细胞株HSC-T6作为体外研究模型,以赤芍水提物给彼格犬一次性灌胃,取给药前的血清、给药后1h、2h、3h、5h血清作为实验药物血清。

Methods: in the experiment, we adopted eternalized human gastric mucosa epithelium ges1 cells transformed by nmethyln'nitronnitrosoguanidine as the model of precancerous lesions for study in vitro.

采用被n甲基n'硝基n亚硝基胍(nmethyln'nitronnitrosoguanidine, mnng)进一步转化后的永生化人胃黏膜上皮细胞系ges1细胞作为胃癌前病变细胞的体外研究模型;以三七水提物给彼格犬一次性灌胃,取给药前的血清、给药后2 h和6 h的血清作为实验药物血清。

From the next day,the explanted animals were administered different agents intraperitoneally.

第2天腹腔注射给药给药结束第2天处死小鼠,完全剥离瘤体,称瘤重,计算抑瘤率。

Injection of rhIL-2 (200,100,50,25,12. 5 ku/kg) can inhibit mouse ear swelling, especially when dosage is 25~50 ku/kg. Injection of rhIL-2 (25 ku/kg) can inhibit rat plantar swelling. The function of mononuclear macrophage system was strengthened by hypodermic injection of rhIL-2( 100 ku/kg) once a day for 9 days. The decrease of mouse delayed-type hypersensitivity reaction induced by cyclophosphamide was extenuated by hypodermic injection of rhIL-2(50 ku/kg) once a day for 6 days. IL-2 has anti-inflammatory effects and immunomodulatory effects when administered in certain dosage.

RhIL-2注射液,剂量为20,10,5,2.5,1.25万u/kg时,对小鼠鼠耳肿胀模型有抑制作用,其中剂量为2.5~5万u/kg时,抑制率最大;剂量为2.5万u/kg时,对大鼠足拓肿胀模型有显著的抑制作用;rhIL-2注射液每日sc用药剂量为10万u/kg,连续给药9d后,可以明显增强小鼠单核吞噬细胞功能;rhIL-2注射液每日sc用药剂量为5万u/kg,连续给药6d后,可明显减轻由免疫抑制剂引起的小鼠迟发性变态反应降低的强度。rhIL-2在一定剂量范围内可以起到抗炎和免疫调节作用。

One week after modeling, rats were medicated once a day for 6 weeks.

各组动物在造模后1周开始给药,1次/d,连续给药6周。

The antibacterial experiments on two bacterial strains of bacterial septicaemia of freshwater fish indicated that the protection rate was 100.0% when the fish was given the medicine first and then infected,and 60.0% or 83.3% if infection was prior to medicining(The content of medicine bath was 3 μ g/mL).

对淡水鱼类细菌性败血症2株致病菌的体内抗菌活性表明:采用药浴用量为3 μg/mL,先给药后感染,保护率为100.0%;先感染后给药,保护率分别为60.0%、83.3%,说明该药对两株菌具有良好的防治作用。

METHODS: Bilateral common carotid arteries of rats in the ischemia and treatment groups were splinted for 30 minutes and reperfused for 1 hour to establish models of isehemic cerebral injury.

缺血组和治疗组大鼠夹闭双侧颈总动脉30min后再灌注1h,建立缺血性脑损伤模型;治疗组在缺血30min前腹腔注射参麦注射液2mL/kg(由红参、麦冬等中药组成);缺血组不给药;对照组做假手术,不夹闭颈总动脉,也不给药

300Mg Calcium L-threonate containing 40mg 〓Ca was given to the subjects shortly after intravenous injection of 4mg 〓Ca chloride solution. Urine samples were collected for 48 hours, and purified by precipitation of ammonium oxalate.

研究中,14名受试者在空腹状态下口服〓Ca标记的L-苏糖酸钙咀嚼片(含300mg元素钙,其中〓Ca 40mg),同时静脉注射含有4mg 〓Ca的氯化钙溶液,分段收集给药前和给药后48小时内的全部尿样。

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