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作 者:汪国忠[1] 胡申江[1] 郑哲岚[2] 孙坚[1] 郑霞[1] 朱朝晖[1] 李江[1] 姚宇玫[1]
机构地区:[1]浙江大学医学院附属第一医院心内科,杭州310003 [2]浙江大学医学院附属第一医院超声影像科,杭州310003
出 处:《生物医学工程学杂志》2006年第4期856-861,共6页Journal of Biomedical Engineering
基 金:浙江省科技厅资助项目(021107817);浙江省科技厅重点科研资助项目(2006C23035)
摘 要:为了提高基因黏附微泡的稳定性和基因携带容量,采用改良超声声振法将质粒-多聚乙酰亚胺(PE I)复合物整合至微泡包膜上而制备出新型载基因微泡。电泳分析及细菌转化实验表明PE I能降低超声声振对质粒结构及功能的破坏。新型载基因微泡具有良好的声学及血液流变学性能,其基因携带量明显高于基因黏附微泡。分别采用超声破裂新型载基因微泡及基因黏附微泡介导心肌细胞β-半乳糖酶基因转染。结果表明,超声破裂载基因微泡能增强裸质粒转染效率达107倍,其基因表达水平为超声破裂基因黏附微泡组的6.85倍。提示经改良法制备的新型载基因微泡是一种安全高效的基因转运载体,超声破裂载基因微泡能明显增强心肌细胞的基因转染效率。To improve the stability and gene-carried capability of gene-attached microbubbles, the method for manufacture of albumin microbubbles was modified and new gene-loaded microbubbles were synthesized by incorporated gene-PEI complex into the shell of microbubbles. Agarose gel electrophoresis and bacteria transformation showed that PEI had the ability to provide the protection of plasmid DNA from ultrasonic degradation. The new gene-loaded microbubbles exhibited excellent acoustical and hemorheological properties. Moreover, they could carry more plasmid DNA than gene-attached microbubbles. β-galactosidase plasmid tansfection into cardiac myocytes was performed by using ultrasound targeted destruction of new gene-loaded microbubbles or gene-attached microbubbles. Gene expression in cardiac myocytes was detected by β-galactosidase in situ staining and quantltlve assay. It was shown that β-galactosidase activity in cardiac myocytes was enhanced 107-fold by ultrasonic destruction of gene-loaded microbubbles compared with naked plasmid transfection and new gene-loaded microbubbles resulted in 6.85-fold increase in β-galactosidase activity compared with optimal transfectlon mediated by gene-attached mlcrobubbles. These results suggested that ultrasonic destruction of the gene-loaded microbubbles can enhance the cardiac myocytes exogenous gene transfer efficiency significantly and new gene-loaded microbubble is an efficient and safe gene delivery vehicle.
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