Co‐micellized Pluronic mixture with thermo‐sensitivity and residence stability as an injectable tissue adhesion barrier hydrogel

• Published in: Journal of biomedical materials research. Part B, Applied biomaterials Vol. 106; no. 1; pp. 172 - 182
• Main Authors: Oh, Se Heang, Kang, Jun Goo, Lee, Jin Ho
• Format: Journal Article
• Language: English
• Published: United States Wiley Subscription Services, Inc 01.01.2018
• Subjects: Additives; Adhesion; Animals; Biocompatibility; Biomedical materials; Body temperature; Cell culture; Hydrogels; Hydrogels - chemistry; Hydrogels - pharmacology; In vivo methods and tests; Injury prevention; Materials research; Materials science; Materials Testing; Micelles; Organs; Poloxamer - chemistry; Poloxamer - pharmacology; Poloxamers; Polyethylene glycol; Polypropylene; Polypropylene glycol; Protective coatings; Rats; Rats, Sprague-Dawley; Sol-gel processes; Stability; Surgery; Tissue Adhesives - chemistry; Tissue Adhesives - pharmacology; Tissues; Wound healing; tissue adhesion; wound healing; Pluronics; hydrogel; adhesion barrier
• ISSN: 1552-4973; 1552-4981; 1552-4981
• DOI: 10.1002/jbm.b.33824

Although the tissue adhesion which leads to various complications frequently occurs after surgery, the development of an ideal tissue adhesion barrier is still a challenge. In this study, a thermo‐sensitive hydrogel, which can fulfill the essential requirements of tissue adhesion barrier (that is, ease of handling for surgeon, flowing down prevention after application, stable residence on the injury during wound healing, and no use of toxic additives), was developed using biocompatible polyethylene glycol‐polypropylene glycol copolymers (Pluronic F127/F68/P123 mixture). From the in vitro cell culture and in vivo animal study, it was observed that the Pluronic mixtures showed sol‐gel transition at approximately body temperature (for easy injection or coating on the injury site and flowing down prevention after application) and prolonged residence stability in aqueous environment (> ∼7 days for stable protection of injury tissues/organs during wound healing), and thus was highly effective for the prevention of tissue adhesion without adverse tissue responses. Based on these results, the Pluronic F127/F68/P123 mixture itself (without any additives) can be a good candidate as an injectable or coatable tissue adhesion barrier hydrogel applicable to various injury tissues in terms of ease of use, effectiveness, and safety. © 2016 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 106B: 172–182, 2018.