Research Group of Nutrition and Health, National Engineering Research Center of Seafood, Dalian Polytechnic University, Dalian 116034, China.
J Mater Chem B. 2023 Nov 8;11(43):10404-10417. doi: 10.1039/d3tb00812f.
Ulcerative colitis (UC) is an inflammatory disease involving ulcers in the colon and rectum. The conventional treatments for UC still have many limitations, such as non-specific release, adverse effects and low absorption, resulting in the poor bioavailability of therapeutic agents. To address these challenges, targeting delivery systems are required to specifically deliver drugs to the colonic site with controlled release. Herein, we present a novel microgel oral delivery system, loaded with liposome nanoparticles (Li NPs) containing a natural anti-inflammatory compound genistein (Gen) into alginate microgels, thereby achieving the targeted release of Gen in the colonic region and ameliorating UC symptoms. Initially, Gen was loaded into phosphatidylserine (PS)-functionalized Li NPs to form Gen@Li NPs with an average size of 245.9 ± 9.6 nm. assessments confirmed that Gen@Li NPs efficiently targeted macrophages and facilitated the internalization of Gen into cells. To prevent rapid degradation in the harsh gastrointestinal tract, Gen@Li NPs were further encapsulated into alginate microgels through electric spraying technology, forming Gen@Li microgels. distribution tests demonstrated that Gen@Li microgels possessed long-term retention in the colon and gradual release characteristics compared to Gen@Li NPs. Furthermore, experiments confirmed that Gen@Li microgels significantly alleviated UC symptoms in mice induced by dextran sulfate sodium salt (DSS) mainly through reducing the expression levels of pro-inflammatory cytokines (TNF-α, IL-1β and IL-6) and promoting colonic mucosal barrier repair through upregulation of mucosal protein expression. This study shed light on the potential of utilizing oral administration of natural compounds for UC treatment.
溃疡性结肠炎(UC)是一种累及结肠和直肠的炎症性疾病。UC 的传统治疗方法仍存在许多局限性,如非特异性释放、不良反应和低吸收率,导致治疗剂的生物利用度较差。为了解决这些挑战,需要靶向递送系统将药物特异性递送到结肠部位并进行控制释放。在此,我们提出了一种新型的微凝胶口服递药系统,将载有天然抗炎化合物染料木黄酮(Gen)的脂质体纳米颗粒(Li NPs)负载到海藻酸钠微凝胶中,从而实现 Gen 在结肠部位的靶向释放,并改善 UC 症状。首先,Gen 被加载到磷脂酰丝氨酸(PS)功能化的 Li NPs 中,形成平均粒径为 245.9±9.6nm 的 Gen@Li NPs。评估证实 Gen@Li NPs 能够有效地靶向巨噬细胞,并促进 Gen 进入细胞内。为了防止在恶劣的胃肠道中快速降解,Gen@Li NPs 进一步通过电喷技术包封到海藻酸钠微凝胶中,形成 Gen@Li 微凝胶。分布测试表明,与 Gen@Li NPs 相比,Gen@Li 微凝胶在结肠中有长期保留和逐渐释放的特点。此外,实验证实 Gen@Li 微凝胶通过降低促炎细胞因子(TNF-α、IL-1β 和 IL-6)的表达水平并通过上调黏膜蛋白表达促进结肠黏膜屏障修复,从而显著缓解了由葡聚糖硫酸钠(DSS)诱导的 UC 症状。本研究为利用口服天然化合物治疗 UC 提供了新的思路。