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

Authors Yang , Gong C , Zhao X, Zhou, Li, Qi, Zhong, Luo F, Qian Z

Received 13 September 2011

Accepted for publication 2 November 2011

Published 2 February 2012 Volume 2012:7 Pages 547—557

DOI https://doi.org/10.2147/IJN.S26141

Review by Single anonymous peer review

Peer reviewer comments 2



Bing Yang1,2*, ChangYang Gong1*, Xia Zhao2, ShengTao Zhou2, ZhengYu Li2, XiaoRong Qi2, Qian Zhong2, Feng Luo1, ZhiYong Qian1
1State Key Laboratory of Biotherapy, West China University Hospital, Sichuan University, Chengdu, People's Republic of China; 2Department of Gynecology and Obstetrics, West China Second University Hospital, Sichuan University, Chengdu, People's Republic of China
*These authors contributed equally in this work

Background: Poly (ethylene glycol)-poly (ε-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, thermosensitive, barrier, biocompatible

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