Reduction of thrombotic and inflammatory complications of polystyrene-block-polyisoprene-block-polystyrene (SIS) with one-step electrospinning

被引:5
|
作者
Wang, Haozheng [1 ,2 ]
Ma, Zhifang [3 ]
Liu, Jingchuan [3 ]
Shi, Qiang [3 ]
Yin, Jinghua [3 ]
机构
[1] Nankai Univ, Key Lab Funct Polymer Mat, Coll Chem, Inst Polymer Chem, Tianjin, Peoples R China
[2] Nankai Univ, State Key Lab Med Chem Biol, Coll Chem, Inst Polymer Chem, Tianjin, Peoples R China
[3] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Polymer Phys & Chem, Changchun, Jilin, Peoples R China
基金
中国国家自然科学基金;
关键词
Polystyrene-block-polyisoprene-block-polystyrene (SIS); thrombotic and inflammatory complications; hemocompatible; reactive oxygen species; reactive electrospinning; THERMOPLASTIC ELASTOMER; IN-VITRO; SURFACE; COPOLYMERS; IMMOBILIZATION; ENDOTHELIUM; ADSORPTION; SEBS;
D O I
10.1080/09205063.2019.1707943
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Polystyrene-block-polyisoprene-block-polystyrene (SIS) has been used as biomaterials due to its soft and stable properties under physiological conditions. However, the thrombotic and inflammatory complications caused by SIS restrain its application as blood-contacting implant. To overcome this problem, the hydrophilic core-shell structured SIS-based microfiber with antioxidant encapsulation is fabricated with one-step reactive electrospinning. We demonstrate that the phase separation of SIS and acylated Pluronic F127 (F127-DA) components and crosslinking during electrospinning renders the microfiber blood compatible and stable under physiological condition; the encapsulation of 2-O-d-glucopyranosyl-l-ascorbic acid (AA-2G) in microfiber and subsequent release of AA-2G detoxifies the excess reactive oxygen species (ROS). The microfibers are nontoxic to cells and promote the fast growth and proliferation of human umbilical vein endothelial cells (HUVECs) in the presence of ROS; the thrombotic and inflammatory complications are effectively reduced with implant evaluation in vivo. Therefore, our work paves a new way to improve the biocompatibility of SIS, making it a promising candidate for blood contact materials.
引用
收藏
页码:642 / 657
页数:16
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