Hyaluronic acid coated teriflunomide (A771726) loaded lipid carriers for the oral management of rheumatoid arthritis

被引:23
作者
Zewail, Mariam [1 ]
EL-Deeb, Nehal M. [2 ]
Mousa, Mohamed R. [3 ]
Abbas, Haidy [1 ]
机构
[1] Damanhour Univ, Fac Pharm, Dept Pharmaceut, Damanhour, Egypt
[2] City Sci Res & Technol Applicat, Genet Engn & Biotechnol Res Inst, Biopharmaceut Prod Res Dept, New Borg El Arab City, Egypt
[3] Cairo Univ, Fac Vet Med, Dept Pathol, Cairo, Egypt
关键词
Immunosuppressive; Active TARGETING; Dmards; Autoimmune diseases; DRUG-DELIVERY; NANOPARTICLES; LEFLUNOMIDE; BIOAVAILABILITY; METABOLITE; RELEASE; SULFATE; NLC;
D O I
10.1016/j.ijpharm.2022.121939
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Systemic rheumatoid arthritis treatment has been associated with numerous side effects. We attempted to formulate hyaluronic acid (HA)-coated teriflunomide (TER)-loaded nanostructured lipid carriers (NLCs) that can target inflamed rheumatic joints following oral administration. In vitro evaluation including colloidal charac-teristics, drug release and stability studies were conducted. Also, cytotoxicity studies on THP1 and peripheral blood mononuclear cells besides testing the binding of HA coated TER-NLCs to CD44 receptors were carried out. Furthermore, pharmacokinetics following oral administration, anti-arthritic effects, hepato and nephrotoxicity of NLCs were assessed. Selected NLCs formulation was approximately 284.9 & PLUSMN; 3.8 nm in size with 96.89 & PLUSMN; 0.45% entrapment effi-ciency and provided a sustained release for 30 days. NLCs showed good stability that was confirmed by TEM examination. Cell culture studies revealed that HA-coated TER-NLCs showed superior cytotoxicity and binding affinity to CD44 receptors compared with TER suspension. In vivo studies demonstrated the superiority of NLCs in increasing TER bioavailability, reducing TNF-alpha serum levels and improving joint healing that was evidenced in both histopathological and X-ray radiographic examination. This may be attributed to the ability of HA-coated TER-NLCs to target rheumatic joints passively and actively by targeting CD44 receptors that are overexpressed in rheumatic joints.
引用
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页数:14
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