林和璞, 王强, 徐维林, 张宏伟, 马晓东. 替莫唑胺-聚乳酸/羟基乙酸纳米缓释系统对C6胶质瘤细胞凋亡的影响[J]. 解放军医学院学报, 2016, 37(2): 164-166,170. DOI: 10.3969/j.issn.2095-5227.2016.02.017
引用本文: 林和璞, 王强, 徐维林, 张宏伟, 马晓东. 替莫唑胺-聚乳酸/羟基乙酸纳米缓释系统对C6胶质瘤细胞凋亡的影响[J]. 解放军医学院学报, 2016, 37(2): 164-166,170. DOI: 10.3969/j.issn.2095-5227.2016.02.017
LIN Hepu, WANG Qiang, XU Weilin, ZHANG Hongwei, MA Xiaodong. Effects of temozolomide-PLGA nanometer sustained-release microsphere on apoptosis of glioma C6 cells[J]. ACADEMIC JOURNAL OF CHINESE PLA MEDICAL SCHOOL, 2016, 37(2): 164-166,170. DOI: 10.3969/j.issn.2095-5227.2016.02.017
Citation: LIN Hepu, WANG Qiang, XU Weilin, ZHANG Hongwei, MA Xiaodong. Effects of temozolomide-PLGA nanometer sustained-release microsphere on apoptosis of glioma C6 cells[J]. ACADEMIC JOURNAL OF CHINESE PLA MEDICAL SCHOOL, 2016, 37(2): 164-166,170. DOI: 10.3969/j.issn.2095-5227.2016.02.017

替莫唑胺-聚乳酸/羟基乙酸纳米缓释系统对C6胶质瘤细胞凋亡的影响

Effects of temozolomide-PLGA nanometer sustained-release microsphere on apoptosis of glioma C6 cells

  • 摘要: 目的 观察替莫唑胺(temozolomide,TMZ)-聚乳酸/羟基乙酸(polylactic acid/glycolic acid,PLGA)缓释微球对胶质瘤细胞活性及凋亡的影响。 方法 将C6胶质瘤细胞样品分为实验组及空白对照组。试验组加入载药量分别为2.5%、5%、7.5%及10%的替莫唑胺-聚乳酸/羟基乙酸缓释微球,空白对照组仅加入PLGA而不加入任何药物。全自动酶标仪检测细胞活性,多参数流式细胞仪分析细胞凋亡率。 结果 2.5%、5%、7.5%及10%实验组在第14天时肿瘤细胞凋亡率分别为30.45%±0.24%、35.87%±0.58%、41.56%±0.82%、43.34%±1.24%,与对照组细胞凋亡率(3.02%±0.24%)相比,均能更有效杀灭C6胶质瘤细胞,并且载药量越高效果越强(P<0.05)。使用MTT法检测各组C6胶质瘤细胞的细胞活性,2.5%、5%、7.5%、10%实验组在第3天时细胞活性分别为23.47%±2.65%、14.58%±5.76%、6.24%±7.32%、4.36%±2.41%,与对照组(99.60%)相比,均能更有效抑制肿瘤细胞活性,且载药量越高效果越强(P<0.05),但7.5%组与10%组差异无统计学意义。 结论 载药量不同的TMZ-PLGA缓释微球均对C6胶质瘤细胞有杀灭作用,一定范围内,载药量越高的缓释微球抑制胶质瘤细胞活性的作用越强。

     

    Abstract: Objective To observe the effect of temozolomide (TMZ) - polylactic acid/glycolic acid (PLGA) release microspheres (MS) on viability and apoptosis of glioma cell. Methods C6 glioma cell samples were divided into experimental group and control group. TMZ - PLGA release microspheres was added into experimental group with the drug loading of 2.5%, 5%, 7.5% and 10%, and only PLGA was added into blank control group. Cell activity was detected with automatic microplate reader and cell apoptosis rate was analyzed with multi-parameter flow cytometry. Results The apoptosis rate of tumor cell in experimental group with drug loading of 2.5%, 5%, 7.5% and 10% on day 14 were 30.45%±0.24%, 35.87%±0.58%, 41.56%±0.82%, 43.34%±1.24%, respectively. Compared with apoptosis rate in control group (3.02%±0.24%), it could kill C6 glioma cells effectively, and the effect enhanced with the increasing of drug loading (P<0.05). The viability of C6 glioma cells detected using MTT was 23.47%±2.65%, 14.58%±5.76%, 6.24%±7.32% and 4.36%±2.41% in experimental group with drug loading of 2.5%, 5%, 7.5% and 10% on day 3, compared with control group (99.60%), the tumor cell activity could be inhibited effectively in experimental groups, and the effect enhanced with the increasing of drug loading (P<0.05), but there was no significant difference between group of 7.5% and group of 10%. Conclusion The C6 glioma cells can be killed by TMZ-PLGA release microspheres of different degree of drug loading. Within a certain range, the higher the drug loading of release microsphere is, the stronger the effect of inhibiting of glioma cells is.

     

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