用户名: 密码: 验证码:
Influence of cytotoxic butyltin complexes with 2-sulfobenzoic acid on the thermotropic phase behavior of lipid model membranes
详细信息    查看全文
  • 作者:Hanna Pruchnik
  • 关键词:Phase transition ; DSC ; Fluidity ; Spectroscopy ; DPPC ; Butyltin complexes with 2 ; sulfobenzoic acid
  • 刊名:Journal of Thermal Analysis and Calorimetry
  • 出版年:2017
  • 出版时间:January 2017
  • 年:2017
  • 卷:127
  • 期:1
  • 页码:507-514
  • 全文大小:716KB
  • 刊物类别:Chemistry and Materials Science
  • 刊物主题:Physical Chemistry; Analytical Chemistry; Polymer Sciences; Inorganic Chemistry; Measurement Science and Instrumentation;
  • 出版者:Springer Netherlands
  • ISSN:1588-2926
  • 卷排序:127
文摘
In the previous study, we showed that butyltin complexes with 2-sulfobenzoic acid (commonly referred to as BTsbz) exhibit a very wide biological activity. The BTsbz in vitro are very active cytotoxic agents against tumor cells—more effective than cisplatin and carboplatin (traditional anticancer drugs). These complexes are antibacterial agents against gram-positive and gram-negative bacteria, as well. The aim of the present study was to investigate the influence of BTsbz on the thermotropic phase behavior of dipalmitoylphosphatidylcholine (DPPC) model membranes. The effect of this compound on the multilamellar liposomes was studied mainly by the means of differential scanning calorimetry and additionally by the steady-state fluorimetry and infrared spectroscopy. All investigated butyltin complexes with 2-sulfobenzoic acid change the thermotropic properties of lipid model membranes: The temperature of the main phase transition of DPPC is slightly decreased, and the transition’s cooperativity of the peak is very much reduced. With increasing concentration, all investigated compounds abolished the pretransition. The results suggest that BTsbz are very active in the hydrophilic area of DPPC bilayer and at the same time have an effect on membrane fluidity.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700