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Research of ALA Combined with HpD-PDT which induced S180 Ascitic Tumor cells, Death or Apoptosis on Cytology

机译:ALA与HPD-PDT结合的研究诱导S180腹水细胞,死亡或细胞凋亡的细胞学

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Objective: To ascertain the adequate dosage of ALA combined with HpD-PDT which induced tumor cell death or apoptosis on cytology. And to study the different effect of ALA-PDT and HPD-PDT used only. Methods: Rat ascitic tumor cells(S180) were randomly divided into several groups and incubated with ALA ( 20μg/ml, 40μg/ml, 80μg/ml, 160μg/ml), HPD( 2.5μg/ml, 5μg/ml, 10μg/ml) and their combination dosages. 630nm light (total output 2W) was delivered to tumor cells at a constant fluence rate: 200mw/cm2 and a constant irradiated time period: 20 minutes. We set 3 groups (no photosensitizers or no irradiation or neither) to be the control groups. We used inversion microscopy to observe the morphological change of tumor cells and flow cytometry technology to detect the death or apoptosis of tumor cells during the experiment... Results: After irradiated with 630nm light on 20 minutes, S180 tumor cells incubated with the combination dosage of ALA 40μg/ml and HPD2.5μg/ml were induced highest rate of apoptosis. The rate of cells' early apoptosis was 2.54%, while the late apoptosis was 95.10% Conclusion: The combination dosage of ALA 40μg/ml and HPD2.5μg/ml(25% of constant dosage) used in the PDT treatment was the most adequate dosage on cytology.
机译:目的:确定ALA与HPD-PDT相结合的足够剂量,诱导肿瘤细胞死亡或细胞学细胞凋亡。并研究Ala-PDT和HPD-PDT仅使用不同的效果。方法:将大鼠腹泻肿瘤细胞(S180)随机分为几组,与ALA(20μg/ ml,40μg/ ml,80μg/ ml,160μg/ ml),HPD(2.5μg/ ml,5μg/ ml,10μg/ ml)及其组合剂量。以恒定的流量速率将630nm光(总输出2W)递送至肿瘤细胞:200mW / cm 2和恒定的照射时间段:20分钟。我们设置了3组(无光敏剂或没有照射或既不)是控制组。我们使用倒置显微镜观察肿瘤细胞的形态变化和流式细胞术技术,检测肿瘤细胞的死亡或凋亡在实验过程中...结果:在20分钟内用630nm灯照射后,S180肿瘤细胞与组合剂量孵育Ala40μg/ ml和HPD2.5μg/ ml诱导最高的凋亡率。细胞早期细胞凋亡的速率为2.54%,而晚期细胞凋亡为95.10%:ALA40μg/ ml和HPD2.5μg/ ml(25%恒定剂量)的组合剂量最适合细胞学剂量的剂量。

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