Local methylprednisolone delivery using a BiodivYsio phosphorylcholine-coated drug-delivery stent reduces inflammation and neointimal hyperplasia in a porcine coronary stent model

Int J Cardiovasc Intervent. 2003;5(3):166-71. doi: 10.1080/14628840310017393.

Abstract

Phosphorylcholine (PC)-coated stents have shown excellent blood and tissue biocompatibility in porcine coronary arteries. The purpose of this study was to determine the efficacy of local methylprednisolone (MP) delivery using PC-coated stents to inhibit inflammatory response and in-stent neointimal hyperplasia in an overstretched porcine coronary model. BiodivYsio (Biocompatibles, Farnham, Surrey, UK) PC-coated drug delivery (DD) stents and DD stents loaded with a high dose of MP (269 microg) were implanted in the coronary arteries of 20 pigs with a balloon/artery ratio of 1.2 : 1. At five days the peri-strut inflammatory response score and thrombus score of the MP-loaded DD stents were lower than in the control stents. The neointimal hyperplasia of MP-loaded DD stents was significantly reduced (0.80 +/- 0.10 versus 0.48 +/- 0.10 mm(2), p < 0.01). At four-week follow-up, the inflammatory response of MP-loaded stents was lower than the control stents, but without significant difference. The MP-loaded stents showed decreased peri-strut arterial injury and in-stent neointimal hyperplasia (2.42 +/- 0.87 versus 1.62 +/- 0.71 mm(2), p < 0.05). It is concluded that local vascular delivery of a high dose of MP from PC-coated DD stents could effectively decrease inflammatory response and thrombus formation after oversized stent deployment and result in a significant reduction of neointimal hyperplasia.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / administration & dosage*
  • Anti-Inflammatory Agents / therapeutic use*
  • Blood Vessel Prosthesis Implantation / adverse effects*
  • Coated Materials, Biocompatible / administration & dosage*
  • Coated Materials, Biocompatible / therapeutic use*
  • Coronary Angiography
  • Coronary Vessels / drug effects*
  • Coronary Vessels / pathology
  • Coronary Vessels / surgery*
  • Disease Models, Animal
  • Drug Delivery Systems / adverse effects*
  • Female
  • Hyperplasia / etiology*
  • Hyperplasia / pathology
  • Hyperplasia / prevention & control*
  • Inflammation / etiology*
  • Inflammation / pathology
  • Inflammation / prevention & control*
  • Male
  • Methylprednisolone / administration & dosage*
  • Methylprednisolone / therapeutic use*
  • Phosphorylcholine / administration & dosage*
  • Phosphorylcholine / therapeutic use*
  • Stents / adverse effects*
  • Swine
  • Time Factors
  • Tunica Intima / drug effects*
  • Tunica Intima / pathology
  • Tunica Intima / surgery*

Substances

  • Anti-Inflammatory Agents
  • Coated Materials, Biocompatible
  • Phosphorylcholine
  • Methylprednisolone