4D Printing of Shape Memory Vascular Stent Based on βCD-g-Polycaprolactone

被引:45
|
作者
Zhou, Yanyi [1 ,2 ]
Zhou, Dong [1 ]
Cao, Pengrui [2 ,3 ]
Zhang, Xinrui [2 ,3 ]
Wang, Qihua [2 ,3 ]
Wang, Tingmei [2 ,3 ]
Li, Zhaolong [1 ]
He, Wenyang [1 ]
Ju, Junping [4 ]
Zhang, Yaoming [2 ,3 ]
机构
[1] Lanzhou Univ Second Hosp, Vasc Surg Dept, Lanzhou 730000, Peoples R China
[2] Chinese Acad Sci, Lanzhou Inst Chem Phys, Key Lab Sci & Technol Wear & Protect Mat, Lanzhou 730000, Peoples R China
[3] Univ Chinese Acad Sci, Ctr Mat Sci & Optoelect Engn, Beijing 100049, Peoples R China
[4] Qingdao Univ, State Key Lab Biofibers & Ecotext, Qingdao 266071, Peoples R China
基金
美国国家科学基金会;
关键词
4D printing; biocompatible stents; drug loaded polymers; shape memory polymers; CYCLODEXTRIN; POLYMERS;
D O I
10.1002/marc.202100176
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The 4D-printing technology is applied to fabricate a shape memory peripheral stent with good biocompatibility, which sustains long-term drug release. The star polymer s-PCL is prepared by ring opening polymerization of epsilon-caprolactone with the -OH of beta-cyclodextrin (beta CD) as initiator, and then the s-PCL is modified with acrylate endgroup which allows the polymerization under UV light to form the crosslinking network c-PCL. Attributed to the feature of the high crosslinked structure and chemical nature of polycaprolactone (PCL) and beta CD, the composite exhibits appropriate tensile strength and sufficient elasticity and bursting pressure, and it is comparable with great saphenous vein in human body. The radial support of the 4D-printed stent is 0.56 +/- 0.11 N and is equivalent to that of commercial stent. The cell adhesion and proliferation results show a good biocompatibility of the stent with human umbilical vein endothelial cells. Due to the presence of beta CD, the wettability and biocompatibility of the materials are improved, and the sustained paclitaxel release based on the host-guest complexion shows the potential of the drug-loaded stent for long-term release. This study provides a new strategy to solve the urgent need of small-diameter scaffolds to treat critical limb ischemia.
引用
收藏
页数:9
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