Graduate School of Science and Technology, Degree Programs in Pure and Applied Sciences, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki 305-8577, Japan; Polymers and Biomaterials Field, Research Center for Functional Materials, National Institute for Materials Science, 1-1 Namiki, Tsukuba, Ibaraki 305-0044, Japan.
Polymers and Biomaterials Field, Research Center for Functional Materials, National Institute for Materials Science, 1-1 Namiki, Tsukuba, Ibaraki 305-0044, Japan.
Acta Biomater. 2022 Sep 1;149:139-149. doi: 10.1016/j.actbio.2022.06.014. Epub 2022 Jun 11.
Postoperative adhesion, bonding of the abdominal wall to damaged organs, causes severe complications after abdominal surgery. Despite the availability of physical barriers (i.e., solutions, films, and hydrogels), adhesion prevention materials that are a single-substance system with stability in wet tissue and ease of use have not been reported. Here, we report a microparticle based, sprayable adhesion prevention material comprising decyl group modified Alaska pollock gelatin (C10-ApGltn). C10-ApGltn microparticles (C10-MPs) were prepared by a coacervation method, freeze drying, and thermal crosslinking. The C10-MPs adhered to and formed a colloidal gel layer on intestinal serosal tissue by hydration without any crosslinking agents. After hydration of the C10-MPs, the resulting colloidal gel layer did not adhere to other tissues. Additionally, the C10-MP colloidal gel layer formed on the stomach serosal tissue showed stability when submersed in saline for 2 days. The colloidal gel layer also showed tissue followability. An in vivo rat adhesion model revealed that C10-MP colloidal gel layer on the cecum and abdominal wall defects effectively reduced postoperative adhesion and induced tissue remodeling, including re-mesothelialization. Therefore, C10-MPs are a potential anti-adhesion material for preventing postoperative adhesion. STATEMENT OF SIGNIFICANCE: We evaluated the postoperative adhesion prevention ability of a colloidal gel based on decyl group modified Alaska pollock gelatin (ApGltn) microparticles (C10-MPs). These microparticles are sprayable and form a colloidal gel with only hydration on the gastrointestinal tissue. We revealed that the modification of the decyl group into ApGltn improved the stability of C10-MP colloidal gel on the tissue by hydrophobic interaction in the in-vitro experiments. The gel prevented postoperative adhesion by being a physical barrier in the in-vivo rat adhesion model.
术后粘连,即腹壁与受损器官的粘连,是腹部手术后严重并发症的原因。尽管有物理屏障(即溶液、薄膜和水凝胶),但尚未报道具有稳定性和易用性的单一物质系统的防粘连材料。在这里,我们报告了一种基于微粒的、可喷涂的防粘连材料,由癸基修饰的阿拉斯加鳕鱼明胶(C10-ApGltn)组成。C10-ApGltn 微粒(C10-MPs)通过共凝聚法、冷冻干燥和热交联制备。C10-MPs 通过水合作用粘附在肠浆膜组织上并形成胶体凝胶层,而无需任何交联剂。C10-MPs 水合后,所得胶体凝胶层不会粘附到其他组织上。此外,C10-MP 胶体凝胶层在胃浆膜组织上形成时,在盐水中浸泡 2 天仍保持稳定。该胶体凝胶层还具有组织追随性。体内大鼠粘连模型表明,C10-MP 胶体凝胶层可有效减少盲肠和腹壁缺损处的术后粘连,并诱导组织重塑,包括再内皮化。因此,C10-MPs 是一种预防术后粘连的潜在防粘连材料。
我们评估了基于癸基修饰的阿拉斯加鳕鱼明胶(ApGltn)微粒(C10-MPs)的胶体凝胶在预防术后粘连方面的能力。这些微粒可喷涂,在胃肠道组织上仅通过水合作用形成胶体凝胶。我们发现,癸基修饰提高了 ApGltn 中 C10-MP 胶体凝胶在组织中的稳定性,这是由于疏水相互作用在体外实验中。该凝胶通过在体内大鼠粘连模型中作为物理屏障来预防术后粘连。