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载他克莫司的 pH 敏感型纳米脂质载体治疗炎症性肠病。

pH-Sensitive Tacrolimus loaded nanostructured lipid carriers for the treatment of inflammatory bowel disease.

机构信息

Department of Pharmacy, Quaid-i-Azam University Islamabad, 45320, Pakistan.

Department of Pharmacy, Quaid-i-Azam University Islamabad, 45320, Pakistan; Faculty of Pharmacy, Capital University of Science & Technology, Islamabad, Pakistan.

出版信息

Eur J Pharm Biopharm. 2024 Nov;204:114461. doi: 10.1016/j.ejpb.2024.114461. Epub 2024 Sep 19.

Abstract

Inflammatory Bowel Disease is the chronic tissue inflammation of the lower part of the Gastrointestinal tract (GIT). Conventional therapeutic approaches face numerous challenges, often making the delivery system inadequate for treating the disease. This study aimed to integrate a pH-sensitive polymer and nanostructured lipid carriers (NLCs) to develop a hybrid nanocarrier system. Tacrolimus-loaded NLCs coated with Eudragit® FS100 (TAC-NLCs/E FS100) nanoparticles were prepared via double emulsion technique followed by an aqueous enteric coating technique. Various parameters, such as particle size, entrapment efficiency, and zeta potential were optimized using Design Expert software®. Cetyltrimethyl ammonium bromide (CTAB) was used as a cationic surfactant which induces a positive charge on the nanoparticles. These cationic NLCs can adhere to the mucosal surface, thereby enabling prolonged retention. In vitro drug release was assessed, and the results demonstrated that drug release was retarded at pH 1.2 corresponding to upper GIT pH and maximum drug was released at pH 7.4 (colonic pH). Moreover, we evaluated TAC-NLCs/E FS100 nanoparticles in murine colitis models to gauge the efficacy of both coated and uncoated NLCs formulation. The TAC-NLCs/E FS100 showed a pronounced reduction in induced colitis, as evident from the restoration of morphological features, improved histopathological scores, antioxidant levels, and decreased the levels of proinflammatory cytokines. Thus, pH-sensitive TAC-NLCs/EFS 100 are attributed to the enhanced localization and targeted delivery at the specific site.

摘要

炎症性肠病是胃肠道(GIT)下部的慢性组织炎症。传统的治疗方法面临许多挑战,通常使递送系统不足以治疗该疾病。本研究旨在整合 pH 敏感聚合物和纳米结构脂质载体(NLC),以开发混合纳米载体系统。通过双重乳液技术制备负载他克莫司的 NLCs 并用 Eudragit® FS100(TAC-NLCs/E FS100)纳米颗粒包衣,随后进行水性肠溶包衣技术。使用 Design Expert software®优化了各种参数,如粒径、包封效率和zeta 电位。十六烷基三甲基溴化铵(CTAB)用作阳离子表面活性剂,可使纳米颗粒带正电荷。这些阳离子 NLCs 可以粘附在粘膜表面,从而实现延长保留时间。评估了体外药物释放,结果表明药物释放在 pH 1.2 时(对应于上 GIT pH)受到抑制,在 pH 7.4(结肠 pH)时最大程度地释放药物。此外,我们在小鼠结肠炎模型中评估了 TAC-NLCs/E FS100 纳米颗粒,以评估涂层和未涂层 NLCs 制剂的功效。TAC-NLCs/E FS100 明显减轻了诱导的结肠炎,这从形态特征的恢复、组织病理学评分的改善、抗氧化水平的提高以及促炎细胞因子水平的降低得到证实。因此,pH 敏感的 TAC-NLCs/EFS 100 归因于在特定部位的增强定位和靶向递送。

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