Table 1

Summary of different surface modifications/coatings for flow diversion and intracranial stents

Surface modificationSummary points
Phosphorylcholine
  • Biopassivity with hydrated boundary layer reducing intrinsic pathway activation

  • Preclinical evidence that it can reduce neointimal hyperplasia

  • Approved for neurovascular use, but unclear safety with SAPT

Glycans
  • Creates hydrophilic boundary layer to reduce intrinsic pathway activation

  • Approved for neurovascular use, including with SAPT in certain geographies. Appears not recommended with aspirin only

  • COATING randomized study ongoing to determine safety/efficacy with prasugrel only

PMEA
  • Prevents interaction with circulating thrombotic factors by forming a protective layer of intermediate water

  • Shown to not impede endothelial attachment

  • Approved for neurovascular use, but unclear safety with SAPT

Immobilized heparin
  • Proven anticoagulant activity of heparin bound to device surface

  • When immobilized, it displays antiplatelet activity as well

  • Devices in the preclinical stage for neurovascular use, but a long history with coronary stents that show safety with aspirin monotherapy

Heparin fibrin nano coating
  • Antithrombogenic coating that is also highly conducive to endothelial growth

  • Approved for neurovascular use, but unclear safety with SAPT

Fxa/GP2b3a inhibitors
  • Powerful antiplatelet and anticoagulant activity

  • Not currently used on medical devices and far from neurovascular implementation

CD-34 antibody
  • Binds endothelial progenitors to improve growth over the device

  • Rapid endothelialization with low stent thrombosis rate

  • Currently only available on coronary devices

Irradiated nitinol
  • Potential to improve endothelial growth and device thrombogenicity by leveraging dissociative water

  • Not currently used on medical devices and far from neurovascular implementation

CD-31 analog
  • Binds endothelial cells to improve growth on device and decreases leukocyte and platelet activation

  • Preclinical stages showing promise

  • PMEA, poly(2-methoxyethyl acrylate); SAPT, single antiplatelet therapy.