目的：建立药物作用下细胞生长抑制率区间估计的数学模型。
Objective: To set up the mathematical model of interval estimation of the inhibitory rate of cell growth under the medical effect.
方法MTT法测定黄芩素对胃癌SGC-7901细胞生长抑制率。
Methods MTT assay was used to determine the cell inhibitory rate.
以氟尿嘧啶组、消瘤汤中剂量组较空白对照组细胞生长抑制率增高显著。
When Xiaoliutang of serum containing low concentrations of drugs, With the inhibition of cell relatively serum containing increasing concentration of the increase.
目的构建顺铂温敏纳米颗粒，表征其相关性质及不同温度下对肿瘤细胞生长抑制率。
Objsctive To prepare cisplatin-loaded thermosensitive nanoparticle and evaluate its characters and cytotoxicity of different temperature in vitro.
结果：随着PDTC干预浓度的增大和时间延长，A549细胞生长抑制率增加（P<0.05、0.01）；
Results: The proliferation inhibitory rate of PDTC on A549 cells increased as incubation time and concentration increasing(P<0.05 or 0.01).
结论BCNU PLGA缓释微球可以抑制C6胶质瘤细胞的增殖，随释放时间延长细胞生长抑制率逐渐上升。
Conclusion BCNU loaded PLGA wafer can inhibit the proliferation of C6 glioma cell and demonstrate gradually increased tendency with prolonged release time.
计算各组细胞死亡率、细胞生长抑制率、克隆形成率并观察形态学变化，应用凝胶电泳、激光扫描共聚焦显微镜观察分析小叶黑柴胡作用MGC- 803细胞后的细胞DNA含量的改变。
The changes of morphology, death rate, the inhibition rate of cell growth, cloning efficiency were observed. DNA content of MGC-803 were measured with the laser scanning confocal microtechnic.
方法：MTT比色法检测肿瘤细胞的生长抑制率；
Methods: The tumor cell growth repression rate was measured by MTT colorimetry.
结果奥沙利铂对CNE - 2细胞的生长抑制率随药物浓度和作用时间的增加而增大。
ResultsThe growth of CNE-2 cells was significantly inhibited by Oxaliplatin in a dose-dependent and time-dependent fashion.
采用MTT法，测定内皮细胞的生长抑制率；
The growth inhibitory rate of endothelial cell was determined by MTT assay;
BDNF基因修饰的大鼠淋巴细胞的培养上清可降低H2O2和DA对PC 12细胞生长的抑制率并能抑制H2O2和DA诱导PC 12细胞凋亡。
ResultsThe supernatant of lymphocytes modified by BDNF gene decreased the growth inhibitory rate and apoptosis rate of PC12 cells induced by H2O2 and DA.
BDNF基因修饰的大鼠淋巴细胞的培养上清可降低H2O2和DA对PC 12细胞生长的抑制率并能抑制H2O2和DA诱导PC 12细胞凋亡。
ResultsThe supernatant of lymphocytes modified by BDNF gene decreased the growth inhibitory rate and apoptosis rate of PC12 cells induced by H2O2 and DA.
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