Abstract

Implantable devices fabricated from austenitic type 316L stainless steel have been employed significantly in medicine, principally because the material displays excellent mechanical characteristics and corrosion resistance. It is well known, however, that interaction of exposure of such a material to blood can initiate platelet adhesion and blood coagulation, leading to a harmful medical condition. In order to prevent undesirable surface platelet adhesion on biomaterials employed in procedures such as renal dialysis, we developed an ultrathin anti-thrombogenic covalently attached monolayer based on monoethylene glycol silane chemistry. This functions by forming an interstitial hydration layer which displays restricted mobility in the prevention of surface fouling. In the present work, the promising anti-thrombogenic properties of this film are examined with respect to platelet aggregation on 316L austenitic stainless steel exposed to whole human blood. Prior to exposure with blood, all major surface modification steps were examined by X-ray photoelectron spectroscopic analysis and surface free-angle measurement by contact angle goniometry. End-stage anti-thrombogenicity detection after 20 min of blood exposure at 100 s−1, 300 s−1, 600 s−1, 750 s−1, and 900 s−1 shear rates revealed that a significant reduction (>90%) of platelet adhesion and aggregation was achieved for surface-modified steel, compared with untreated material. This result is confirmed by experiments conducted in real time for 60-minute exposure to blood at 100 s−1, 600 s−1, and 900 s−1 shear rates.

Highlights

  • We demonstrate that an ultrathin monoethylene glycol (MEG-OH), which is covalently attached to the steel surface, is capable of a dramatic reduction in platelet aggregation from blood

  • All glassware involved in the silanization process was pre-treated with 5% (v/v) octadecyltrichlorosilane (OTS) in anhydrous toluene inside a glove box maintained under inert atmosphere. 2-(3-trichlorosilylpropyloxy) ethyl-trifluoroacetate (MEG-trifluoroacetic acid (TFA)) linker used for stainless steel surface silanization was synthesized as described previously [42]

  • Surface characterization by X-ray photoelectron spectroscopic (XPS) and contact angle goniometry has confirmed the successful modification of steel samples with MEG-OH coatings

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Summary

Introduction

Coronary artery disease (CAD) is a debilitating condition where a buildup of plaque forms which causes the occurrence of arterial narrowing (stenosis) [1]. A significant number of solutions have been developed to prevent stenosis from occurring, including coronary bypass surgery, balloon angioplasty, as well as coronary stents [2]. The poor biocompatibility of bare metal stents (BMS) has prevented the successful integration of this implant amongst all patients suffering from stenosis. Upon implantation of a bare metal stent, the artery undergoes re-narrowing, known as restenosis. Thrombus formation and cell injury during percutaneous transluminal coronary angioplasty (PTCA) are all factors contributing to the occurrence of restenosis [3,4,5]

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