Shamiya Yasmeen, Chakraborty Aishik, Zahid Alap Ali, Bainbridge Nicholas, Guan Jingyuan, Feng Biao, Pjontek Dominic, Chakrabarti Subrata, Paul Arghya
Department of Chemistry, The University of Western Ontario, London, ON Canada.
Department of Chemical and Biochemical Engineering, The University of Western Ontario, London, ON Canada.
Commun Mater. 2024;5(1):197. doi: 10.1038/s43246-024-00641-x. Epub 2024 Sep 20.
Nanofiber-based hydrogel delivery systems have recently shown great potential in biomedical applications, specifically due to their high surface-to-volume ratio of ultra-fine nanofibers and their ability to carry low solubility drugs. Herein, we introduce a visible light-triggered in situ-gelling drug vehicle (GAP Gel) composed of ascorbyl palmitate (AP) nanofibers and gelatin methacryloyl polymer. AP nanofibers form self-assembled structures through intermolecular interactions with a hydrophobic drug-loading core. We demonstrate that the hydrophilic periphery of AP nanofibers allows them to interact with other hydrophilic molecules via hydrogen bonds. The presence of AP nanofibers significantly enhances the viscoelasticity of GAP Gel in a concentration-dependent manner. Further, GAP Gel shows in vitro biocompatibility and sustained drug delivery efficacy when loaded with a hydrophobic antibiotic. Likewise, GAP Gel shows excellent in vivo biocompatibility when implanted in immunocompetent mice in various forms. Lastly, GAP Gels maintain cell viability when cultured in a 3D-environment over 7 days, establishing it as a promising and versatile hydrogel platform for the delivery of biotherapeutics.
基于纳米纤维的水凝胶递送系统最近在生物医学应用中显示出巨大潜力,特别是由于其超细纳米纤维的高比表面积以及携带低溶解度药物的能力。在此,我们介绍一种由抗坏血酸棕榈酸酯(AP)纳米纤维和甲基丙烯酰化明胶聚合物组成的可见光触发原位凝胶化药物载体(GAP凝胶)。AP纳米纤维通过与疏水性药物负载核心的分子间相互作用形成自组装结构。我们证明,AP纳米纤维的亲水性外围使其能够通过氢键与其他亲水性分子相互作用。AP纳米纤维的存在以浓度依赖的方式显著增强了GAP凝胶的粘弹性。此外,当负载疏水性抗生素时,GAP凝胶显示出体外生物相容性和持续药物递送功效。同样,当以各种形式植入具有免疫活性的小鼠体内时,GAP凝胶显示出优异的体内生物相容性。最后,GAP凝胶在三维环境中培养7天以上时能维持细胞活力,使其成为一种用于生物治疗递送的有前途且通用的水凝胶平台。