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骨髓单个核细胞分化为CD103^+树突状细胞的方法研究(英文)
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作者 陈云秀 吴毅 +5 位作者 彭欣 孔潇 李媛媛 田小银 张光莉 罗征秀 《广西医科大学学报》 CAS 2019年第12期1882-1888,共7页
目的:探索小鼠骨髓单个核细胞在体外培养诱导其分化为CD103^+树突状细胞(DCs)的方法,为免疫性疾病的防治提供实验基础。方法:分离小鼠胫腓骨,冲洗骨髓腔得到骨髓细胞,利用单个核细胞分离液分离出单个核细胞,加入粒细胞巨噬细胞集落刺激... 目的:探索小鼠骨髓单个核细胞在体外培养诱导其分化为CD103^+树突状细胞(DCs)的方法,为免疫性疾病的防治提供实验基础。方法:分离小鼠胫腓骨,冲洗骨髓腔得到骨髓细胞,利用单个核细胞分离液分离出单个核细胞,加入粒细胞巨噬细胞集落刺激因子(GM-CSF)、Fms样酪氨酸激酶3配体(FLT3L)诱导其分化为成熟的DCs。显微镜下观察细胞大小、形态、分布,流式细胞术检测细胞CD103^+及其共刺激分子的表达水平,再利用磁珠分选出CD103^+DCs,检测其纯度。结果:单个核细胞培养8 d后,倒置显微镜下观察到细胞分化为多种形态,大部分呈圆形或不规则,大小不一,细胞周围有细小凸起,成簇状分布,细胞表面CD11c和CD103增多,表面标志物CD40、CD80、CD86和MHC-Ⅱ升高,磁珠分选纯化后CD103^+DCs纯度可达95.7%,分选后的CD103^+DCs可有效促进T细胞分化。结论:利用GM-CSF和FLT3L联合诱导法进行体外培养,能够得到纯度较高的CD103^+DCs。 展开更多
关键词 单个核细胞 CD103^+ DCs GM-CSF FLT3L
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Efficient degradation of drug ibuprofen through catalytic activation of peroxymonosulfate by Fe_3C embedded on carbon 被引量:2
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作者 guangli zhang Yaobin Ding +1 位作者 Wenshan Nie Heqing Tang 《Journal of Environmental Sciences》 SCIE EI CAS CSCD 2019年第4期1-12,共12页
Ibuprofen(IBU),a nonsteroidal anti-inflammatory drug,is becoming an important member of pharmaceuticals and personal care products(PPCPs)as emerging pollutants.To degrade IBU,magnetic Fe_3C nanoparticles embedded on N... Ibuprofen(IBU),a nonsteroidal anti-inflammatory drug,is becoming an important member of pharmaceuticals and personal care products(PPCPs)as emerging pollutants.To degrade IBU,magnetic Fe_3C nanoparticles embedded on N-doped carbon(Fe_3C/NC)were prepared as a catalyst by a sol–gel combustion method.As characterized,the Fe_3C/NC nanoparticles were composed of a NC nano-sheet and capsulated Fe_3C particles on the sheet.The Fe_3C/NC nanoparticles were confirmed an efficient catalyst for peroxymonosulfate(PMS)activation to generate sulfate radicals(SO_4^(·-)),single oxygen(~1O_2)and hydroxyl radicals(·OH)toward the degradation of IBU.The added IBU(10 mg/L)was almost completely removed in 30 min by using 0.1 g/L Fe_3C/NC and 2 g/L PMS.The catalyst was confirmed to have good ability and excellent reusability through leaching measurements and cycle experiments.A catalytic mechanism was proposed for the catalytic activation of PMS on Fe_3C/NC,which involves both Fe_3C reactive sites and N-doped carbon matrix as reactive sites in Fe_3C/NC.Moreover,the degradation pathway of IBU in the Fe_3C/NC-PMS system was proposed according to the detections of degradation intermediates. 展开更多
关键词 CATALYTIC degradation IBUPROFEN Iron CARBIDE N-DOPED CARBON PEROXYMONOSULFATE
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