Injectable and Sprayable Albumin/Serum Hydrogels that Demonstrate the Complete Coverage of a Wound and Possess Dynamically and Spatially Controllable Material Properties for the Prevention of Post-Operative Adhesion

S. Mao, Weicai Yan, Hui-wen Peng, Chi-Shuo Chen, Ying-Chieh Chen
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引用次数: 1

Abstract

Since the degree of severity and geometry of wounds vary, it is necessary to prepare an anti-adhesive hydrogel that possesses dynamically controllable material properties, exhibits biodegradability, and possesses drug-releasing properties. Injectable, sprayable, oxygen peroxide (H2O2)-sensitive and photo-cross-linkable hydrogels that permit in situ dynamic and spatial control of their physicochemical properties were synthesized for the prevention of postoperative adhesion. Albumin is the most abundant protein in blood serum and serves as a carrier for a number of molecules that exhibit poor water solubility. It is therefore a suitable biomaterial for the fabrication of hydrogels since it presents a low risk of life-threatening complications and does not require immunosuppressive therapy for preventing graft rejection. As micromolar concentrations of endogenous H2O2 are produced after tissue damage, aqueous pre-polymer solutions that exhibit solution-to-gel transition behaviors in response to H2O2 were developed. These solutions form a thin layer of hydrogel that fully covers the wound site and acts as a barrier. The physicochemical properties of this hydrogel can then be spatially post-adjusted via transdermal exposure to light to release drugs, depending on what is required for the particular injury. A significant reduction in postoperative peritoneal adhesion was observed in an animal model involving severe sidewall and bowel abrasions. This study demonstrated that the fabricated dually cross-linked, albumin-based hydrogels have great potential in such applications because they showed a low immune response, easy handling, full wound coverage, and tunable biodegradability. Precise spatial and controllable drug-release profiles may also be achieved via in situ transdermal post-tuning of the biomaterials, depending on the injury.
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可注射和喷雾的白蛋白/血清水凝胶,可完全覆盖伤口,并具有动态和空间可控的材料特性,可预防术后粘连
由于伤口的严重程度和几何形状各不相同,因此有必要制备一种具有动态可控材料特性,具有生物降解性和药物释放特性的抗粘附水凝胶。合成了可注射、可喷涂、对过氧化氧(H2O2)敏感、可光交联的水凝胶,这些水凝胶允许对其物理化学性质进行原位动态和空间控制,以防止术后粘连。白蛋白是血清中含量最多的蛋白质,是许多水溶性较差分子的载体。因此,它是一种适合制造水凝胶的生物材料,因为它具有低风险的危及生命的并发症,并且不需要免疫抑制治疗来防止移植排斥。由于组织损伤后会产生微摩尔浓度的内源性H2O2,因此研究人员开发出了在H2O2作用下表现出溶液到凝胶转变行为的水性预聚合物溶液。这些溶液形成一层薄薄的水凝胶,完全覆盖伤口,起到屏障的作用。这种水凝胶的物理化学性质可以根据特定损伤的需要,通过透皮暴露在光线下释放药物,在空间上进行后期调整。在涉及严重侧壁和肠道磨损的动物模型中,观察到术后腹膜粘连显著减少。该研究表明,制备的双交联白蛋白基水凝胶具有很大的应用潜力,因为它们具有低免疫反应,易于处理,完全覆盖伤口和可调节的生物降解性。精确的空间和可控的药物释放谱也可以通过生物材料的原位透皮后调整来实现,具体取决于损伤。
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