4.7 Article

Physically Cross-Linked Hyaluronan-Based Ultrasoft Cryogel Prepared by Freeze-Thaw Technique as a Barrier for Prevention of Postoperative Adhesions

Journal

BIOMACROMOLECULES
Volume 22, Issue 12, Pages 4967-4979

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.biomac.1c00878

Keywords

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Funding

  1. National Nature Science Foundation of China [21774075, 21074071]
  2. China Postdoctoral Science Foundation [2020M681308, 2020T130411, 2021M692211]

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Various studies have shown that physical anti-adhesion barriers like hydrogels can effectively reduce or prevent postsurgical peritoneal adhesions, while the use of chemical cross-linkers in chemical hydrogels may lead to cytotoxicity or unwanted side effects. A physically cross-linked hyaluronan cryogel was developed as a novel anti-adhesion biomaterial, demonstrating excellent biocompatibility and preventing fibroblast penetration, with the ability to inhibit inflammatory responses and modulate the fibrinolytic system to prevent peritoneal adhesions.
Postsurgical peritoneal adhesions are a common and serious postoperative complication after various peritoneal surgeries, such as pelvic and abdominal surgery. Various studies have shown that peritoneal adhesions can be minimized or prevented by physical anti-adhesion barriers, including membranes, knits, and hydrogels. Hydrogels have attracted great attention in preventing peritoneal adhesions because the dimensional architecture of hydrogels is similar to that of the native extracellular matrix. However, chemical cross-linkers had to be used in the preparation of chemical hydrogels, which may have problems in cytotoxicity or unwanted side effects. This fact prompts us to create alternative cross-linking methods for the development of biocompatible hydrogels as physical barriers. Herein, we report a physically cross-linked flexible hyaluronan (HA) cryogel prepared via a freeze-thaw technique as a novel anti-adhesion biomaterial for completely preventing postsurgical peritoneal adhesions. In vitro studies demonstrated that this physically cross-linked HA cryogel exhibited excellent biocompatibility, the inherently desirable biocompatibility and functionality of HA being integrally retained as much as possible. Intriguingly, the rheological properties and appropriate biodegradability of the cryogels were readily tailored and tunable by way of the gelation process. In vivo assessments suggested that the cryogel, as a physical barrier, satisfactorily prevented fibroblast penetration and attachment between the injured tissues and nearby normal organs. Furthermore, the molecular mechanism studies revealed that the HA cryogel could prevent peritoneal adhesion by inhibiting inflammatory response and modulation of the fibrinolytic system. Our results show that HA ultrasoft cryogel is a promising clinical candidate for prolonged adhesion prevention.

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