中国组织工程研究
中國組織工程研究
중국조직공정연구
Journal of Clinical Rehabilitative Tissue Engineering Research
2015年
12期
1846-1851
,共6页
生物材料%纳米材料%生物相容性%氨基化修饰%CCK-8%细胞毒性%荧光染色%国家自然科学基金
生物材料%納米材料%生物相容性%氨基化脩飾%CCK-8%細胞毒性%熒光染色%國傢自然科學基金
생물재료%납미재료%생물상용성%안기화수식%CCK-8%세포독성%형광염색%국가자연과학기금
Nanostructures%Materials Testing%Lanthanoid Series Elements
背景:与有机荧光染料和荧光蛋白相比,稀土纳米材料具有更高的灵敏性和更好的光学稳定性,并且具有更低的细胞毒性。目的:探讨(Y 0.95 Eu 0.05)2 O 3方法:采用溶胶-凝胶法合成(Y稀土纳米材料的体外细胞相容性,以及氨基化修饰对材料细胞相容性的影响。0.95 Eu 0.05)2 O 3稀土纳米材料,并进行氨基化修饰。将10,25,50,100,200 mg/L的氨基化与非氨基化(Y0.95Eu0.05)2O3稀土纳米材料悬液分别与SD大鼠血管平滑肌细胞共培养3 d, CCK-8法检测细胞增殖;将100 mg/L的氨基化与非氨基化(Y0.95Eu0.05)2O3结果与结论:随着材料悬液质量浓度的升高,血管平滑肌细胞存活率呈逐渐减少趋势;在材料质量浓度为10,25,50 mg/L时,氨基化组细胞存活率明显高于未氨基化组(P<0.05);当材料质量浓度高达200 mg/L时,未氨基化组细胞存活率降到76%,氨基化组细胞存活率仍然在80%以上,两组比较差异有显著性意义(P<0.05)。氨基化组L929细胞生长状况良好,凋亡细胞数量较少;未氨基化组生长较稀疏,细胞凋亡数量较多,显示出轻微的细胞毒性。表明氨基化修饰可以有效提高(Y稀土纳米材料悬液分别与L929细胞共培养48 h,荧光染色观察细胞凋亡。0.95Eu0.05)2O3稀土纳米材料的细胞相容性。
揹景:與有機熒光染料和熒光蛋白相比,稀土納米材料具有更高的靈敏性和更好的光學穩定性,併且具有更低的細胞毒性。目的:探討(Y 0.95 Eu 0.05)2 O 3方法:採用溶膠-凝膠法閤成(Y稀土納米材料的體外細胞相容性,以及氨基化脩飾對材料細胞相容性的影響。0.95 Eu 0.05)2 O 3稀土納米材料,併進行氨基化脩飾。將10,25,50,100,200 mg/L的氨基化與非氨基化(Y0.95Eu0.05)2O3稀土納米材料懸液分彆與SD大鼠血管平滑肌細胞共培養3 d, CCK-8法檢測細胞增殖;將100 mg/L的氨基化與非氨基化(Y0.95Eu0.05)2O3結果與結論:隨著材料懸液質量濃度的升高,血管平滑肌細胞存活率呈逐漸減少趨勢;在材料質量濃度為10,25,50 mg/L時,氨基化組細胞存活率明顯高于未氨基化組(P<0.05);噹材料質量濃度高達200 mg/L時,未氨基化組細胞存活率降到76%,氨基化組細胞存活率仍然在80%以上,兩組比較差異有顯著性意義(P<0.05)。氨基化組L929細胞生長狀況良好,凋亡細胞數量較少;未氨基化組生長較稀疏,細胞凋亡數量較多,顯示齣輕微的細胞毒性。錶明氨基化脩飾可以有效提高(Y稀土納米材料懸液分彆與L929細胞共培養48 h,熒光染色觀察細胞凋亡。0.95Eu0.05)2O3稀土納米材料的細胞相容性。
배경:여유궤형광염료화형광단백상비,희토납미재료구유경고적령민성화경호적광학은정성,병차구유경저적세포독성。목적:탐토(Y 0.95 Eu 0.05)2 O 3방법:채용용효-응효법합성(Y희토납미재료적체외세포상용성,이급안기화수식대재료세포상용성적영향。0.95 Eu 0.05)2 O 3희토납미재료,병진행안기화수식。장10,25,50,100,200 mg/L적안기화여비안기화(Y0.95Eu0.05)2O3희토납미재료현액분별여SD대서혈관평활기세포공배양3 d, CCK-8법검측세포증식;장100 mg/L적안기화여비안기화(Y0.95Eu0.05)2O3결과여결론:수착재료현액질량농도적승고,혈관평활기세포존활솔정축점감소추세;재재료질량농도위10,25,50 mg/L시,안기화조세포존활솔명현고우미안기화조(P<0.05);당재료질량농도고체200 mg/L시,미안기화조세포존활솔강도76%,안기화조세포존활솔잉연재80%이상,량조비교차이유현저성의의(P<0.05)。안기화조L929세포생장상황량호,조망세포수량교소;미안기화조생장교희소,세포조망수량교다,현시출경미적세포독성。표명안기화수식가이유효제고(Y희토납미재료현액분별여L929세포공배양48 h,형광염색관찰세포조망。0.95Eu0.05)2O3희토납미재료적세포상용성。
BACKGROUND:Compared with organic fluorescent dyes and fluorescent proteins, rare earth nanomaterials have higher sensitivity, better optical stability, and lower cytotoxicity. OBJECTIVE: To investigate thein vitro cytocompatibility of (Y0.95Eu0.05)2O3 METHODS:(Y rare earth nanomaterial and the effect of amine functionalization on the material cytocompatibility. 0.95Eu0.05)2O3 nanomaterials were synthesized using sol-gel method, and underwent amine functionalization. Amine-functionalized samples (10, 25, 50, 100, 200 mg/L) and non-amine-functionalized (Y0.95Eu0.05)2O3 rare earth nanomaterial suspensions were co-cultured with vascular smooth muscle cels of Sprague-Dawley rats for 3 days. Cel proliferation was detected using Cel Counting Kit-8 assay. 100 mg/L amine-functionalized samples and non-amine-functionalized (Y0.95Eu0.05)2O3 rare earth nanomaterial suspensions were co-cultured with L929 cels for 48 hours. Cel apoptosis was observed using fluorescence staining. RESULTS AND CONCLUSION:With increased mass concentration of material suspension, survival rate of vascular smooth muscle cels was gradualy reduced. At the mass concentration of 10, 25, 50 mg/L, cel survival rate was significantly higher in the amine-functionalized group than in the non-amine-functionalized group (P < 0.05). When the mass concentration of materials reached 200 mg/L, the cel survival rate decreased to 76% in the non-amine-functionalized group, but it was stil above 80% in the amine-functionalized group, showing significant differences between the two groups (P < 0.05). The growth of L929 cels was good and the number of apoptotic cels was less in the amine-functionalized group. Cels were sparse and the number of cel apoptosis was more in the non-amine-functionalized group, showing slight cytotoxicity. These data verified that amine-functionalization can improve cytocompatibility of (Y0.95Eu0.05)2O3 rare earth nanomaterial.