Neduri Karthik, Ailuno Giorgia, Zuccari Guendalina, Bassi Anna Maria, Vernazza Stefania, Schito Anna Maria, Caviglioli Gabriele, Baldassari Sara
Department of Pharmacy, University of Genova, 16148 Genova, Italy.
Department of Experimental Medicine, University of Genova, 16132 Genova, Italy.
Pharmaceutics. 2024 Oct 19;16(10):1342. doi: 10.3390/pharmaceutics16101342.
BACKGROUND/OBJECTIVES: Oral diseases causing mucosal lesions are normally treated with local or systemic anti-inflammatory, analgesic and antimicrobial agents. The development of topical formulations, including wound-healing promoters, might speed up the recovery process, improving patients' quality of life, and reduce the risk of deterioration in health conditions. In this study, a mucoadhesive multilayer film, including a novel biocompatible substance (solubilized eggshell membrane, SESM), was rationally designed.
The SESM preparation procedure was optimized and its biological effects on cell proliferation and inflammation marker gene expression were evaluated in vitro; preformulation studies were conducted to identify the most promising polymers with film-forming properties; then, trilayer films, consisting of an outer layer including chlorhexidine digluconate as a model drug, a supporting layer and a mucoadhesive layer, incorporating SESM, were prepared using the casting method and their mechanical, adhesion and drug release control properties were evaluated.
SESM proved to possess a notable wound-healing capacity, inducing a wound closure of 84% in 24 h without inhibiting blood clotting. The films revealed a maximum detachment force from porcine mucosa of approx. 1.7 kPa and maximum in vivo residence time of approx. 200-240 min; finally, they released up to 98% of the loaded drug within 4 h.
The formulated trilayer films were found to possess adequate properties, making them potentially suitable for protecting oral lesions and favoring their rapid healing, while releasing antimicrobial substances that might be beneficial in reducing the risk of bacterial infections.
背景/目的:引起黏膜损伤的口腔疾病通常采用局部或全身抗炎、止痛和抗菌药物进行治疗。包括伤口愈合促进剂在内的局部制剂的开发可能会加速恢复过程,提高患者的生活质量,并降低健康状况恶化的风险。在本研究中,合理设计了一种包含新型生物相容性物质(可溶性蛋壳膜,SESM)的黏膜黏附多层膜。
优化了SESM的制备工艺,并在体外评估了其对细胞增殖和炎症标志物基因表达的生物学作用;进行了处方前研究,以确定最有前景的具有成膜性能的聚合物;然后,采用流延法制备了由外层(包含作为模型药物的葡萄糖酸氯己定)、支撑层和包含SESM的黏膜黏附层组成的三层膜,并评估了其机械性能、黏附性能和药物释放控制性能。
SESM被证明具有显著的伤口愈合能力,在24小时内可使伤口闭合84%,且不抑制血液凝固。这些膜显示出与猪黏膜的最大分离力约为1.7 kPa,体内最大停留时间约为200 - 240分钟;最后,它们在4小时内释放了高达98%的负载药物。
所制备的三层膜具有足够的性能,使其有可能适用于保护口腔损伤并促进其快速愈合,同时释放抗菌物质,这可能有助于降低细菌感染的风险。