Huang Kang-Ting, Fang Yun-Lung, Hsieh Pai-Shan, Li Chun-Chang, Dai Niann-Tzyy, Huang Chun-Jen
Department of Biomedical Sciences and Engineering, National Central University, Jhong-Li, Taoyuan 320, Taiwan.
J Mater Chem B. 2016 Jun 21;4(23):4206-4215. doi: 10.1039/c6tb00302h. Epub 2016 May 27.
In this study, zwitterionic poly(sulfobetaine acrylamide) (pSBAA) nanocomposite hydrogels were synthesized and implemented as effective chronic wound dressings. The hydrogels exhibited reinforced mechanical properties from added hectorite nanoclay as a physical crosslinker in the polymer chains. Due to the strong interaction with water molecules via ionic solvation, the hydration of the zwitterionic nanocomposite hydrogels was superior to the non-ionic 2-hydroxyethyl methacrylate (pHEMA) hydrogels, which interacts with water molecules via hydrogen bonding. The pSBAA nanocomposite hydrogels cytotoxicity was accessed with NIH-3T3 fibroblast by the MTT assay, the results indicated negligible cytotoxicity after incubation for three days. In addition, the zwitterionic hydrogels displayed evident resistance to adsorption of bovine serum albumin (BSA), NIH-3T3 fibroblast, and bacteria of gram positive S. epidermidis and gram negative P. aeruginosa. The need for antifouling properties in a wound dressing is because commercial dressings removal typically damaging newly formed tissues and colonization of microorganisms occurs on the dressings. For clinical applications as wound dressings, we created normal and diabetic wounds on mice and compared newly developed pSBAA nanocomposite hydrogels with commercial available products. We demonstrated that non-adhesive pSBAA nanocomposite hydrogels enabled ready wound surface removal. Moreover, the wound recovery was conducted with normal and diabetic wounds on rat dorsal by visual observation and showed a complete heal after 10 and 12 days, respectively. Moreover, the histological examination of mice skin confirmed that the zwitterionic hydrogels exhibited thorough re-epithelialization and total formation of new connective tissues in the normal and diabetic wounds after 10 and 12 days, respectively, which was faster than commercial dressings. Consequently, we demonstrated that the pSBAA nanocomposite can serve as an effective dressing for wound management.
在本研究中,合成了两性离子聚(磺基甜菜碱丙烯酰胺)(pSBAA)纳米复合水凝胶,并将其用作有效的慢性伤口敷料。由于在聚合物链中添加了锂皂石纳米粘土作为物理交联剂,水凝胶表现出增强的机械性能。由于通过离子溶剂化与水分子的强相互作用,两性离子纳米复合水凝胶的水合作用优于通过氢键与水分子相互作用的非离子甲基丙烯酸2-羟乙酯(pHEMA)水凝胶。通过MTT法用NIH-3T3成纤维细胞评估pSBAA纳米复合水凝胶的细胞毒性,结果表明孵育三天后细胞毒性可忽略不计。此外,两性离子水凝胶对牛血清白蛋白(BSA)、NIH-3T3成纤维细胞以及革兰氏阳性表皮葡萄球菌和革兰氏阴性铜绿假单胞菌具有明显的抗吸附性。伤口敷料需要具备防污性能,原因在于商业敷料的去除通常会损害新形成的组织,并且微生物会在敷料上定植。对于作为伤口敷料的临床应用,我们在小鼠身上制造了正常伤口和糖尿病伤口,并将新开发的pSBAA纳米复合水凝胶与市售产品进行了比较。我们证明了非粘性的pSBAA纳米复合水凝胶能够轻松去除伤口表面。此外,通过肉眼观察对大鼠背部的正常伤口和糖尿病伤口进行伤口恢复情况评估,结果显示分别在10天和12天后完全愈合。此外,对小鼠皮肤的组织学检查证实,两性离子水凝胶分别在10天和12天后在正常伤口和糖尿病伤口中表现出完全的重新上皮化和新结缔组织的完全形成,这比商业敷料更快。因此,我们证明了pSBAA纳米复合材料可作为伤口处理的有效敷料。