Preventing postoperative abdominal adhesions in a rat model with PEG-PCL-PEG hydrogel

Int J Nanomedicine. 2012:7:547-57. doi: 10.2147/IJN.S26141. Epub 2012 Feb 2.

Abstract

Background: Poly (ethylene glycol)-poly (ɛ-caprolactone)-poly (ethylene glycol) (PEG-PCL-PEG, PECE) hydrogel has been demonstrated to be biocompatible and thermosensitive. In this study, its potential efficacy and mechanisms of preventing postsurgical abdominal adhesions were investigated.

Results: PECE hydrogel was transformed into gel state from sol state in less than 20 seconds at 37°C. None of the animals treated with the hydrogel (n = 15) developed adhesions. In contrast, all untreated animals (n = 15) had adhesions that could only be separated by sharp dissection (P < 0.001). The hydrogel adhered to the peritoneal wounds, gradually disappeared from the wounds within 7 days, and transformed into viscous fluid, being completely absorbed within 12 days. The parietal and visceral peritoneum were remesothelialized in about 5 and 9 days, respectively. The hydrogel prevented the formation of fibrinous adhesion and the invasion of fibroblasts. Also, along with the hydrogel degradation, a temporary inflammatory cell barrier was formed which could effectively delay the invasion of fibroblasts during the critical period of mesothelial regeneration.

Conclusion: The results suggested that PECE hydrogel could effectively prevent postsurgical intra-abdominal adhesions, which possibly result from the prevention of the fibrinous adhesion formation and the fibroblast invasion, the promotion of the remesothelialization, and the hydroflotation effect.

Keywords: anti-adhesion; barrier; biocompatible; thermosensitive.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Abdominal Cavity / pathology
  • Animals
  • Biocompatible Materials / adverse effects
  • Biocompatible Materials / chemistry
  • Biocompatible Materials / therapeutic use
  • Epithelium / pathology
  • Female
  • Fibrosis / pathology
  • Histocytochemistry
  • Phase Transition
  • Polyesters / adverse effects
  • Polyesters / chemistry
  • Polyesters / therapeutic use*
  • Polyethylene Glycols / adverse effects
  • Polyethylene Glycols / chemistry
  • Polyethylene Glycols / therapeutic use*
  • Postoperative Complications / drug therapy
  • Postoperative Complications / pathology
  • Postoperative Complications / prevention & control*
  • Rats
  • Rats, Wistar
  • Statistics, Nonparametric
  • Temperature
  • Tissue Adhesions / drug therapy
  • Tissue Adhesions / pathology
  • Tissue Adhesions / prevention & control*

Substances

  • Biocompatible Materials
  • Polyesters
  • poly(ethylene glycol)-poly(caprolactone)-poly(ethylene glycol)
  • Polyethylene Glycols