• The therapeutic effect and its mechanism of anti-silica tablet, a chinese medicine was studied by hemolysis test.

    本文利用溶血试验方法探讨了中药抗矽治疗矽肺疗效及作用机理

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  • The hemocompatibility of modified PU films was evaluated using hemolysis test and the dynamic blood clotting test.

    通过溶血试验动态凝血试验来改性前后聚氨酯血液相容性进行评价。

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  • The blood compatibility of material was studied in rabbit blood by hemolysis test and platelet adhesion experiment.

    采取新鲜通过溶血实验血小板黏附实验研究材料血液相容性

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  • Experiments on the acute toxicity and hemolysis test of the eel show that the material possesses good biocompatibility.

    急性毒性溶血试验合格,表明材料具有良好生物相容性

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  • Methods the methods used in this study as following: the venous and muscular stimulation test, the allergy test and the hemolysis test.

    方法采用静脉注射血管刺激性肌肉注射刺激性、过敏试验溶血试验。

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  • Methods To evaluate the biocompatibility through acute toxicity test, pyrogen test, hemolysis test and muscle and bone implantation test.

    方法去细胞基质进行急性毒性实验热源实验、溶血实验、兔肌肉种植实验兔桡骨骨缺损修复实验研究。

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  • Cell growth rate test and hemolysis test were conducted to investigate the cytotoxicity and hemolysis reaction for skin reproducing membrane.

    其方法是采用细胞增殖度试验溶血试验,对医用丝素蛋白皮肤再生进行细胞毒性和溶血反应的实验研究

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  • METHODS: Compound Shenshao injection was studied through adoption of the hemolysis test stipulated by the pharmacologic empirical methodology.

    方法根据药理实验方法学规定溶血性试验方法,以复方参芍注射剂研究对象进行试验。

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  • Methods the safety of Clindamycin Phosphate injection was evaluated by the allergy test, venous and muscle stimulation test and hemolysis test.

    方法采用过敏试验静脉血管刺激试验、肌肉刺激试验、溶血试验观察克林霉素磷酸酯安全性

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  • Methods The safety was assassed in animals by pharmacological assays such as allergy reaction test, venous and muscular stimulation test, and hemolysis test.

    方法采用变态反应实验静脉血管刺激实验、肌肉刺激实验、溶血实验进行毒理学研究。

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  • In the safety evaluation, the results of red blood cell hemolysis test and chorioallantioc membrane experiment showed that the hemp leaf extract was not irritative.

    安全性评价中,红细胞溶血试验鸡胚绒毛尿囊试验结果表明汉麻提取物无明显刺激性。

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  • Methods Recalcification test, hemolysis test and platelet adhesive test were conducted for compact silk membrane, polyporous silk membrane, bovine pericardium and collagen sponge.

    方法将致密丝素多孔丝素膜和对照组的心包、蚀原海绵行复钙试验溶血试验、血小板粘附试验。

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  • METHODS: the biological safety was evaluated through the experiments including hemolysis test, short-term systemic toxicity test, oral mucous membrane irritation test and cytotoxicity test (MTT test).

    方法:分别通过溶血试验口腔黏膜刺激试验、细胞毒性试验(MTT法)急性全身毒性试验,初步评价纯钛表面聚吡咯涂层的生物安全性

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  • Methods Recalcification, hemolysis and platelet adhesive test were conducted for the compact silk membrane, porous silk membrane, bovine pericardium and collagen sponge.

    方法将致密丝素多孔丝素对照组心包、蚀原海绵行复钙、溶血血小板粘附试验

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  • Expressed protein was analyzed with SDS PAGE. Hemolysin test was performed to determine the hemolysis activity.

    SDSPAGE分析蛋白表达溶血试验检测表达蛋白的溶血活性。

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  • Objective To study the influence, interference and corrective measures of different hemolysis sample on the accuracy of conventional chemical test.

    目的探讨不同溶血标本对临床常规化学检验准确性影响干扰纠正措施

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  • Methods: Biocompatibility of the natural bone derived material were investigated by the acute and subacute toxicity test, hemolysis and coagulation test and muscle stimulation test.

    方法:本实验应用急性毒性试验亚急性毒性试验、血液相容性试验、肌肉刺激试验等,对生物衍生材料组织相容性进行评价。

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  • Method ABO hemolysis was diagnosed through test for the umbilical cord.

    方法取新生儿脐血作血清学检查判断abo溶血病。

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  • Among hemolysis three tests, the positive rates of direct coombs test, free antibody test and antibody release test were 44%(88/200), 28%(56/200) and 62.5%(125/200) respectively.

    溶血三项试验直接抗人球蛋白试验阳性88例,阳性率为44%(88/200),血清游离抗体试验阳性56例,阳性率为28%(56/200),抗体释放试验阳性125例,阳性率为62.5%(125/200)。

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  • The blood in the procoagulant inert separation tube (yellow cap) was more likely to hemolysis than that in the sodium citrate coagulation test tube (blue cap).

    惰性分离(黄色封盖)枸橼酸试验管(蓝色封盖)更易溶血。

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  • The blood in the procoagulant inert separation tube (yellow cap) was more likely to hemolysis than that in the sodium citrate coagulation test tube (blue cap).

    惰性分离(黄色封盖)枸橼酸试验管(蓝色封盖)更易溶血。

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