Jeong Jae-Pil, Kim Kyungho, Kim Jaeyul, Kim Yohan, Jung Seunho
Department of Bioscience and Biotechnology, Konkuk University, Seoul 05029, Republic of Korea.
Polymers (Basel). 2023 Jul 11;15(14):3009. doi: 10.3390/polym15143009.
We fabricated new hydrogels using polyvinyl alcohol (PVA) and succinoglycan (SG) directly isolated and obtained from Rm 1021 via the freeze-thaw method. Both the composition of the hydrogels and the freeze-thaw cycles were optimized to maximize the swelling ratio for the preparation of the PVA/SG hydrogels. During the optimization process, the morphology and conformational change in the hydrogel were analyzed by scanning electron microscopy, rheological measurements, and compressive tests. An optimized hydrogel with a maximum swelling ratio of 17.28 g/g was obtained when the composition of PVA to SG was 50:50 (PVA/SG 50/50) and the total number of freeze-thaw cycles was five. The PVA/SG 50/50 hydrogel had the largest pore with 51.24% porosity and the highest cross-over point (28.17%) between the storage modulus (G') and the loss modulus (G″). The PVA/SG 50/50 hydrogel showed improved thermal stability owing to its interaction with thermally stable SG chains. The improvement in the thermal stability was confirmed by thermogravimetric analysis and differential scanning calorimetry. In addition, the PVA/SG 50/50 hydrogel showed differential drug release according to the corresponding pH under acidic conditions of pH 1.2 and slightly basic conditions of pH 7.4. Furthermore, the cell viability test on the HEK-293 cell line for that hydrogel demonstrated that the PVA/SG 50/50 hydrogel was non-toxic and biocompatible. Therefore, this hydrogel could be a potential scaffold capable of pH-responsive drug delivery for chronic wound dressing applications.
我们使用直接从Rm 1021中分离并获得的聚乙烯醇(PVA)和琥珀聚糖(SG),通过冻融法制备了新型水凝胶。对水凝胶的组成和冻融循环进行了优化,以最大化PVA/SG水凝胶制备过程中的溶胀率。在优化过程中,通过扫描电子显微镜、流变学测量和压缩试验分析了水凝胶的形态和构象变化。当PVA与SG的组成比例为50:50(PVA/SG 50/50)且冻融循环总数为五次时,获得了最大溶胀率为17.28 g/g的优化水凝胶。PVA/SG 50/50水凝胶具有最大的孔隙,孔隙率为51.24%,储能模量(G')和损耗模量(G'')之间的交叉点最高(28.17%)。由于与热稳定的SG链相互作用,PVA/SG 50/50水凝胶表现出改善的热稳定性。热重分析和差示扫描量热法证实了热稳定性的提高。此外,PVA/SG 50/50水凝胶在pH 1.2的酸性条件和pH 7.4的弱碱性条件下表现出根据相应pH的药物释放差异。此外,对该水凝胶在HEK-293细胞系上的细胞活力测试表明,PVA/SG 50/50水凝胶无毒且具有生物相容性。因此,这种水凝胶可能是一种潜在的支架,能够用于慢性伤口敷料应用的pH响应性药物递送。