期刊文献+

高浓度纳米羟基磷灰石凝胶对Hela肿瘤细胞的作用 被引量:2

Effect of high-concentration nano hydroxyapatite sol on Hela cells
下载PDF
导出
摘要 背景:有文献质疑羟基磷灰石凝胶浓度越高杀死癌细胞的能力越强。目的:观察不同质量浓度纳米羟基磷灰石凝胶对Hela肿瘤细胞的杀伤作用。方法:采用化学沉淀法制备5,10,20,40,80,160,320,640mg/L不同质量浓度的纳米羟基磷灰石凝胶,分别加入Hela细胞中,以在Hela细胞中加入5,10mg/L紫杉醇为对照。结果与结论:①不同质量浓度纳米羟基磷灰石凝胶对Hela肿瘤细胞均有杀伤作用,且随着质量浓度的提高,杀伤作用也逐渐提高,但其对肿瘤细胞的生长抑制作用不及紫杉醇。②纳米羟基磷灰石凝胶与紫杉醇对Hela肿瘤细胞杀伤作用在第2天有所下降,第3天又呈现提高趋势,且第3天的抑制作用较第1天更明显,并且所有质量浓度的纳米羟基磷灰石凝胶均呈现这个趋势。③纳米羟基磷灰石凝胶对Hela肿瘤细胞的生长有一定抑制作用,紫杉醇作用后细胞不呈现明显增殖,纳米羟基磷灰石凝胶作用后细胞有不同程度增殖。 BACKGROUND:Several literatures have questioned that with the increase of nano hydroxyapatite sol concentration,the capacity of killing tumor cells becomes stronger.OBJECTIVE:To investigate the killing effect of nano hydroxyapatite sol with different concentrations on Hela cells.METHODS:Nano hydroxyapatite sol with the concentrations of 5,10,20,40,80,160,320 and 640 μg/mL were synthesized by the chemical precipitation method and added into the Hela cells.The Hela cells added with 5 and 10 mg/L taxol served as controls.RESULTS AND CONCLUSION:①Nano hydroxyapatite sol with different concentrations had killing effect on Hela cells;as the concentration of nano hydroxyapatite sol increased;the killing effect was gradually improved.But their inhibited effect was not better than that of taxol.②The killing effect of nano hydroxyapatite sol and the taxol on Hela cells began decreased at day 2,but it increased in the following day.The inhibited effect at day 3 was more obvious than that at day 1,and nano hydroxyapatite sol with various concentrations were all showed this tendency.③A certain inhibited effect of nano hydroxyapatite sol on Hela cells was found.The proliferation of Hela cells was not significant after given taxol,while Hela cells were found proliferation in various degrees after given nano hydroxyapatite sol.
出处 《中国组织工程研究》 CAS CSCD 2012年第38期7063-7067,共5页 Chinese Journal of Tissue Engineering Research
基金 泸州医学院附属医院提供的资金资助
  • 相关文献

参考文献18

二级参考文献140

共引文献97

同被引文献23

  • 1袁媛,唐胜利,洪华,刘昌胜.纳米羟基磷灰石的制备及其抗肿瘤活性的研究[J].中国生物医学工程学报,2005,24(1):26-30. 被引量:19
  • 2Murugan R, Ramakrishna S. Development of nanocom- posites for bone grafting [J]. Composites Science and Technology, 2005, 65 (15/16) : 2385-2406.
  • 3Vallet-Regf M, Gonz~tlez-Calbet J]M, Calcium phos- phates as substitution of bone tissues [J]. Progress in Sol- id State Chemistry, 2004, 32(1/2) : 1-31.
  • 4Kim S S, Park iVl S, Jeon O, et al. Poly(lactide-co-gly- colide)/hydroxyapatite composite scaffolds for bone tissue engineering [J]. Biomaterials, 2006, 27 ( 8 ) : 1399 - 1409.
  • 5Hench L L, Wilson J. An introduction to bioceramics [M ]. London :World Scientific, 1993.
  • 6Tas A C. Synthesis of biomimetic Ca-hydroxyapatite pow- der at 37 ~C in synthetic body fluids [J]. Biomaterials, 2000, 21 (lg) : 1429-1438.
  • 7Yu J]H, Chu X B, Cai Y R, et al. Preparation and char- acterization of antimicrobial nano-hydroxyapatite compos- ites[J]. Materials Science and Engineering C, 2014, 37 : 54-59.
  • 8Liu D M, Yang Q Z, Troczynski T, et al. Structural evo- lution of sol-gel-derived hydroxyapatite[J]. Biomaterials, 2002, 23(7): 1679-1687.
  • 9Lim G K, Wang J, Ng S C, et al. Processing of fine hydroxyapatite powders via an inverse microemulsion route [J]. Materials Letters, 1996, 28 (4/6) : 431-436.
  • 10Munarin F, Petrinia P, Gentilini R, et al. Micro- and nano-hydroxyapatite as active reinforcement for soft bio- composites[J]. International Journal of Biological Macro- molecules, 2015, 72: 199-209.

引证文献2

二级引证文献9

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部