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基于质量源于设计的来优化特立氟胺和槲皮素组合的经皮传递体用于治疗类风湿性关节炎。

Quality by design-based optimization of teriflunomide and quercetin combinational topical transferosomes for the treatment of rheumatoid arthritis.

作者信息

Karnam Sriravali, Jindal Anil B, Paul Atish T

机构信息

Department of Pharmacy, Birla Institute of Technology and Science, Pilani (BITS-Pilani), Pilani Campus, Rajasthan 333031, India.

Department of Pharmacy, Birla Institute of Technology and Science, Pilani (BITS-Pilani), Pilani Campus, Rajasthan 333031, India.

出版信息

Int J Pharm. 2024 Dec 5;666:124829. doi: 10.1016/j.ijpharm.2024.124829. Epub 2024 Oct 13.

Abstract

Rheumatoid arthritis (RA) is an immune-mediated inflammatory disease. Combination therapy is anticipated to surpass monotherapy by targeting multiple pathways involved in RA progression. The present aim is to develop a combination of Teriflunomide (TFD) and Quercetin (QCN) loaded transferosomal gel to enhance permeability and achieve localized delivery to joint tissues. TFD or QCN transferosomes were optimized employing a 3-level, 3-factorial design Box-Behnken design (BBD). The transferosomes exhibited sustained in-vitro drug release. The topical combination gel underwent thorough evaluation of rheology, and also ex-vivo studies showed enhanced permeability through rat skin. The synergistic combination of TFD and QCN effectively suppressed NO, TNF-α and IL-6 levels in in-vitro RAW 264.7 cells. The cytotoxicity in HaCaT cell lines indicates non-toxicity of the gel, further confirmed by skin irritation study conducted in rats. The in-vivo anti-arthritic activity was evaluated in complete freund's adjuvant induced rat paw edema model illustrates the effectiveness of the combination transferosomal gel compared to other treatment groups. In conclusion, the topical delivery of TFD and QCN combination transferosomal gel demonstrated anti-arthritic activity through localized delivery whichallows for dose reduction, thereby may reduce the systemic drug exposure and mitigate the side effects associated with oral administration of TFD.

摘要

类风湿性关节炎(RA)是一种免疫介导的炎症性疾病。联合治疗预计通过靶向参与 RA 进展的多个途径超过单药治疗。本研究旨在开发一种负载有特立氟胺(TFD)和槲皮素(QCN)的传递体凝胶的组合,以增强通透性并实现局部递送至关节组织。采用 3 水平 3 因素 Box-Behnken 设计(BBD)对 TFD 或 QCN 传递体进行优化。传递体表现出持续的体外药物释放。局部联合凝胶对流变学进行了彻底评估,并且还进行了离体研究表明通过大鼠皮肤增强了通透性。TFD 和 QCN 的协同组合有效地抑制了体外 RAW 264.7 细胞中 NO、TNF-α 和 IL-6 的水平。HaCaT 细胞系中的细胞毒性表明凝胶无毒性,通过在大鼠中进行皮肤刺激性研究进一步证实。在完全弗氏佐剂诱导的大鼠足肿胀模型中评估了体内抗关节炎活性,表明与其他治疗组相比,组合传递体凝胶的局部递送具有抗关节炎活性。总之,TFD 和 QCN 联合传递体凝胶的局部递送通过局部递送显示出抗关节炎活性,允许减少剂量,从而可能减少全身药物暴露并减轻与 TFD 口服给药相关的副作用。

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