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Light-responsive vesicles for enantioselective release of chiral drugs prepared from a supra-amphiphilic M-helix.

Tengfei YanFei LiShuaiwei QiJun TianRuizhen TianJinxing HouQuan LuoZeyuan DongJiayun XuJunqiu Liu
Published in: Chemical communications (Cambridge, England) (2019)
A kind of light-responsive vesicle was prepared by aqueous self-assembly of α-CD and an azobenzene-containing M-helical foldamer, which displayed dynamic disassembly-reassembly structural transformation when alternately irradiated by UV and visible light. Distinctively, this vesicle also exhibited enantioselective release abilities toward racemic propranolol (a β-blocker), owing to the M-helical building blocks.
Keyphrases
  • visible light
  • cancer therapy
  • ionic liquid
  • dna binding
  • angiotensin converting enzyme
  • mass spectrometry
  • angiotensin ii
  • nk cells
  • transcription factor