Department of Chemistry, Himachal Pradesh University, Shimla 171005, India.
Department of Chemistry, Himachal Pradesh University, Shimla 171005, India.
Int J Biol Macromol. 2024 Oct;277(Pt 3):134396. doi: 10.1016/j.ijbiomac.2024.134396. Epub 2024 Aug 2.
The main focus of the present research is to design network hydrogels derived from natural polymers to promote a sustainable future. Multifunctional hydrogels were prepared by combining sterculia gum (SG), phosphorester -cyclic amide polymers for bio-medical applications including drug delivery (DD). The antibiotic drug ceftriaxone was incorporated into hydrogels to enhance wound healing potential. The surface morphology of copolymers was investigated by using FESEM and AFM techniques. FTIR and C NMR spectroscopic techniques provided insight into the formation of network structures. In FTIR analysis, distinctive bands were identified: at 1649 cm attributed to CO stretching of the cyclic amide of PVP, at 1147 cm and 974 cm representing PO stretching and P-O-C of poly(BMEP), respectively. In the C NMR spectrum, a prominent peak at 63.272 ppm revealed the presence of (O-CH) linkage of poly(BMEP). XRD demonstrated amorphous characteristics of hydrogels. The interactions of copolymer with blood, bio-membrane and encapsulated drug illustrated their biocompatibility, bio-adhesion and controlled DD properties. The dressings expressed a hemolytic index value of 2.58 ± 0.03 %. The hydrogels exhibited mucoadhesive character, revealed from the adhesion force of 50.0 ± 5 mN needed to separate polymer dressing from the mucosa. Dressings exhibited antioxidant properties and displayed 33.73 ± 0.3 % radical scavenging in the DPPH assay. Protein adsorption test of copolymer illustrated 9.48 ± 0.970 % of albumin adsorption. The tensile strength of the dressing was found 0.54 ± 0.03 N mm while the burst strength 9.92 ± 0.27 N was observed. The sustained release of the drug was provided by supra-molecular interactions. Drug release followed a non-Fickian diffusion mechanism and the release profile was best described by the Higuchi kinetic model. Additionally, hydrogel dressings revealed permeability to HO vapors and O and antimicrobial activity. These findings suggest the suitability of sterculia gum-based hydrogels for DD uses.
本研究的主要重点是设计源自天然聚合物的网络水凝胶,以促进可持续的未来。通过将乌桕胶(SG)与磷酯-环酰胺聚合物结合,制备了多功能水凝胶,可用于包括药物输送(DD)在内的生物医学应用。将抗生素药物头孢曲松掺入水凝胶中以提高伤口愈合潜力。使用 FESEM 和 AFM 技术研究共聚物的表面形态。FTIR 和 C NMR 光谱技术提供了对网络结构形成的深入了解。在 FTIR 分析中,鉴定了特征谱带:在 1649 cm -1处归因于 PVP 环酰胺的 CO 拉伸,在 1147 cm -1和 974 cm -1处分别代表 PO 拉伸和聚(BMEP)的 P-O-C。在 C NMR 谱中,在 63.272 ppm 处的强峰表明存在聚(BMEP)的(O-CH)键合。XRD 证明了水凝胶的无定形特征。共聚物与血液、生物膜和包封药物的相互作用表明了它们的生物相容性、生物粘附性和控制 DD 特性。敷料的溶血指数值为 2.58 ± 0.03%。水凝胶表现出粘液粘附特性,从将聚合物敷料从粘膜上分离所需的 50.0 ± 5 mN 的粘附力可以看出。敷料表现出抗氧化性能,并在 DPPH 测定中显示 33.73 ± 0.3%的自由基清除率。共聚物的蛋白质吸附测试表明,白蛋白吸附率为 9.48 ± 0.970%。敷料的拉伸强度为 0.54 ± 0.03 N mm,而破裂强度为 9.92 ± 0.27 N。药物的缓释是通过超分子相互作用提供的。药物释放遵循非 Fickian 扩散机制,释放曲线最符合 Higuchi 动力学模型。此外,水凝胶敷料显示出对 HO 蒸气和 O 的渗透性以及抗菌活性。这些发现表明,基于乌桕胶的水凝胶适用于 DD 用途。