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关节内双重药物递送协同治疗类风湿性关节炎。

Intra-Articular Dual Drug Delivery for Synergistic Rheumatoid Arthritis Treatment.

机构信息

Department of Pharmaceutics, Faculty of Pharmacy, Damanhour University, El Gomhoria Street, Damanhour, Egypt.

Department of Pharmaceutics, Faculty of Pharmacy, Alexandria University, Alexandria, Egypt; Department of Pharmaceutics, Faculty of Pharmacy, Kuwait University, Kuwait.

出版信息

J Pharm Sci. 2021 Jul;110(7):2808-2822. doi: 10.1016/j.xphs.2021.04.001. Epub 2021 Apr 20.

DOI:10.1016/j.xphs.2021.04.001
PMID:33848528
Abstract

Systemic rheumatoid arthritis (RA) regimens fail to attain effective drug level at the affected joints and are associated with serious side effects. Herein, an attempt made to improve therapeutic outcomes of both leflunomide (LEF) which is a disease modifying antirheumatic and dexamethasone (Dex) through local delivery of combination therapy by intra-articular route. LEF and Dex were encapsulated in nanostructured lipid carriers (NLCs) and PLGA nanoparticles (NPs), respectively. Both nanocarriers were loaded into chitosan/β glycerophosphate (CS/βGP) thermo-sensitive hydrogels and injected intra-articularly in adjuvant induced RA rat model. Particle size of LEF NLCs and selected Dex NPs formulations were 200 and 119 nm, respectively. Dex NPs and LEF NLCs showed a sustained release profile for up to 58 and 17 days, respectively. After 14 days of treatment remarkable joint healing was observed for groups treated with Dex NPs in combination with either free LEF or LEF NLCs in CS/βGP hydrogel. Joint diameter measurements, TNF α levels and histopathological examination of dissected joints showed comparable values to the negative control group. This might be attributed to the synergistic effect of drug combination besides the ability of nanocarriers loaded hydrogel to prolong joint residence time and enhance joint healing potential.

摘要

系统性类风湿关节炎 (RA) 治疗方案未能在受影响的关节达到有效的药物水平,并伴有严重的副作用。在此,我们尝试通过关节内局部递送来改善来氟米特 (LEF) 和地塞米松 (Dex) 的治疗效果,LEF 是一种疾病修饰抗风湿药,Dex 是一种皮质类固醇。LEF 和 Dex 分别被包封在纳米结构脂质载体 (NLC) 和 PLGA 纳米颗粒 (NPs) 中。两种纳米载体都被加载到壳聚糖/β甘油磷酸酯 (CS/βGP) 温敏水凝胶中,并在佐剂诱导的 RA 大鼠模型中关节内注射。LEF NLCs 的粒径和选定的 Dex NPs 制剂分别为 200nm 和 119nm。Dex NPs 和 LEF NLCs 分别显示出长达 58 天和 17 天的持续释放。在治疗 14 天后,用 Dex NPs 联合游离 LEF 或 LEF NLCs 治疗的组在 CS/βGP 水凝胶中观察到显著的关节愈合。关节直径测量、TNF-α 水平和解剖关节的组织病理学检查显示与阴性对照组相当的值。这可能归因于药物联合的协同作用,以及负载纳米载体的水凝胶延长关节停留时间和增强关节愈合潜力的能力。

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