产品展厅收藏该商铺

您好 登录 注册

当前位置:
美国布鲁克海文仪器公司>资料下载>Nanobrook Omni测量应用案例-25

资料下载

Nanobrook Omni测量应用案例-25

阅读:196          发布时间:2018-6-21
提 供 商 美国布鲁克海文仪器公司 资料大小 1MB
资料图片 下载次数 38次
资料类型 PDF 文件 浏览次数 196次
免费下载 点击下载    
 文献名: Cytosolic Delivery of Doxorubicin from Liposomes to Multidrug-Resistant Cancer Cells via Vaporization of Perfluorocarbon Droplets

 

作者 Jacob B Williams1, Clara M Buchanan1, Ghaleb Husseini2 and William G Pitt1

1 Department of Chemical Engineering, Brigham Young University, USA

2 Department of Chemical Engineering, American University of Sharjah, UAE

 

摘要:A  common  mechanism  of  multidrug  resistance  is  the  upregulation  of  efflux  pumps in the cancer cells that can more rapidly export unwanted materials (e.g. cancer  drugs)  out  of  the  cell,  compared  to  sensitive  cancer  cells.  This  research  seeks  to  overcome  this  mechanism  by  vaporizing  a  perfluoropentane  emulsion  droplet inside of a drug-containing liposome (eLiposome) that was endocytosed into  a  cancer  cell.  Folate  attached  to  the  eLiposome  facilitates  uptake  into  the  cell as observed by confocal microscopy. Ultrasound was examined as a trigger to initiate the vaporization of the perfluoropentane droplet and release doxorubicin from  folated  eLiposomes  (feLD).  Two  seconds  of  ultrasound  released  78%  of  encapsulated  doxorubicin  from  feLD.  Doxorubicin-sensitive  KB-3-1  cells  and  doxorubicin-resistant  KB-V1  cells  treated  with  feLD  (without  ultrasound)  had  cell viabilities of 33% and 60%, respectively. Ultrasound had negligible additional effect on the cell viability of KB-3-1 and KB-V1 cells treated with feLD (33% and 53%, respectively). We hypothesized that the doxorubicin sulfate fibers that were formed  during  the  loading  of  doxorubicin  into  the  eLiposome  present  a  site  for  heterogeneous  nucleation  once  the  feLD  is  endocytosed  by  the  cell,  and  thus  droplet vaporization occurs with or without ultrasound.

收藏该商铺

登录 后再收藏

提示

您的留言已提交成功!我们将在第一时间回复您~

对比框

产品对比 产品对比 联系电话 二维码 意见反馈 在线交流

扫一扫访问手机商铺
010-62081908
在线留言