Literature DB >> 27932703

An in vivo pilot study of a microporous thin film nitinol-covered stent to assess the effect of porosity and pore geometry on device interaction with the vessel wall.

Youngjae Chun1,2, Colin P Kealey3, Daniel S Levi4, David A Rigberg5, Yanfei Chen1, Bryan W Tillman5, K P Mohanchandra6, Mahdis Shayan1, Gregory P Carman6.   

Abstract

Sputter-deposited thin film nitinol constructs with various micropatterns were fabricated to evaluate their effect on the vessel wall in vivo when used as a covering for commercially available stents. Thin film nitinol constructs were used to cover stents and deployed in non-diseased swine arteries. Swine were sacrificed after approximately four weeks and the thin film nitinol-covered stents were removed for histopathologic evaluation. Histopathology revealed differences in neointimal thickness that correlated with the thin film nitinol micropattern. Devices covered with thin film nitinol with a lateral × vertical length = 20 × 40 µm diamond pattern had minimal neointimal growth with well-organized cell architecture and little evidence of ongoing inflammation. Devices covered with thin film nitinol with smaller fenestrations exhibited a relatively thick neointimal layer with inflammation and larger fenestrations showed migration of inflammatory and smooth muscle cells through the micro fenestrations. This "proof-of-concept" study suggests that there may be an ideal thin film nitinol porosity and pore geometry to encourage endothelialization and incorporation of the device into the vessel wall. Future work will be needed to determine the optimal pore size and geometry to minimize neointimal proliferation and in-stent stenosis.

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Keywords:  Coronary artery disease; neointimal hyperplasia; peripheral artery disease; restenosis; thin film nitinol

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Year:  2016        PMID: 27932703     DOI: 10.1177/0885328216682691

Source DB:  PubMed          Journal:  J Biomater Appl        ISSN: 0885-3282            Impact factor:   2.646


  1 in total

1.  Nitinol thin films functionalized with CAR-T cells for the treatment of solid tumours.

Authors:  Michael E Coon; Sirkka B Stephan; Vikas Gupta; Colin P Kealey; Matthias T Stephan
Journal:  Nat Biomed Eng       Date:  2019-12-09       Impact factor: 25.671

  1 in total

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