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Dilation-Responsive Microshape Programing Prevents Vascular Graft Stenosis.

Se Won YiYoung Min ShinJung Bok LeeJu Young ParkDae-Hyun KimWooyeol BaekJeong-Kee YoonDeok Gie KimIn Sik ShinChang-Soo KimMi-Lan KangJae Won YangHak-Joon Sung
Published in: Small (Weinheim an der Bergstrasse, Germany) (2021)
Shape memory materials have been successfully applied to minimally invasive implantation of medical devices. However, organ-movement-specific shape programing at a microscale level has never been demonstrated despite significant unmet needs. As vein-to-artery grafting induces vein dilation and stenosis, a polymeric self-enclosable external support (SES) is designed to wrap the vascular out-wall. Its micropores are programmed to increase sizes and interconnections upon dilation. Vessel dilation promotes venous maturation, but overdilation induces stenosis by disturbed blood flow. Therefore, the unique elastic shape-fixity of SES provides a foundation to enable a stable microscale shape transition by maintaining the vein dilation. The shape transition of micropore architecture upon dilation induces beneficial inflammation, thereby regenerating vasa vasorum and directing smooth muscle cell migration toward adventitia with the consequent muscle reinforcement of veins. This game-changer approach prevents the stenosis of vein-to-artery grafting by rescuing ischemic disorders and promoting arterial properties of veins.
Keyphrases
  • blood flow
  • smooth muscle
  • cell migration
  • minimally invasive
  • cancer therapy
  • skeletal muscle
  • inferior vena cava
  • working memory
  • subarachnoid hemorrhage
  • drug release