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1)  In vitro and in vivo evaluation methods
体内外试验
2)  in vitro
体外试验
1.
Hemocompatibility of biomaterial designed for the closure of congenital heart defects covalently coated by chitosan/heparin:an evaluation in vitro;
壳聚糖/肝素共价包被先天性心脏病介入封堵材料血液相容性的体外试验研究
2.
Objective To explore the effects of 2,3,5,4'-tetrahydroxy stilbene-2-β-D-glycoside(TSG)on the over-expression and aggregation of α-synuclein in vitro.
目的观察二苯乙烯苷(TSG)在体外试验中对COS-7细胞株过度表达α-synuclein蛋白的影响。
3)  In vitro experiment
体外试验
4)  in vitro Test
体外试验
1.
Methods Preparing 2 kinds of Ca-P/SR composites:Hydroxyapatite/SR(HA/SR)、β-Tricalcium phosphate(β-TCP/SR),observing the microstructure by scanning electron microscope and some short-time in vitro tests such as hemolysis test,acute systematic toxicity test were detected to evaluate the biocomtibility of Ca-P/SR composites.
目的制备钙磷陶瓷/硅橡胶复合材料,对材料进行形貌分析和短期体外试验,了解其微观结构和生物安全性。
5)  test in vitro
体外试验
6)  in vitro
体内试验
1.
In vitro,the mice hepatocytes were treated with DCA for 1 hour and then were tested by comet assay;In vivo,DCA were administerd to mices one time in a day lasting six days.
方法 :小鼠肝细胞的体外、体内试验。
补充资料:体内抗菌试验
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性质:指试验动物体内感染细菌最小致死菌量能引起发病过程的药物治疗效果,是药效学重要指标。药物治疗试验分为全身感染和局部感染两种。前者如腹腔或静脉内感染致死菌量后,分若干组,未给药组以动物死亡作对照。治疗分若干剂量组,给药次数根据药效而定,一般根据剂量组存活动物数能测出半数有效量(ED50)为宜。后者如肺部、尿路、皮肤、肌肉、心内膜及其他部位感染等,均能产生炎症病理改变,药物治疗、给药次数及途径、疗程均与全身感染相似。疗效指标有动物存活数、局部病变程度、清除细菌数量等。根据判断指标,可求出ED50

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