4.4 Article

Design and Evaluation of Continentalic Acid Encapsulated Transfersomal Gel and Profiling of its Anti-arthritis Activity

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AAPS PHARMSCITECH
卷 24, 期 7, 页码 -

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SPRINGER
DOI: 10.1208/s12249-023-02648-y

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lipid-based formulation; permeation enhancer; skin permeability; topical route; transfersomes

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This research developed Continentalic acid-loaded transfersomes embedded in Carbopol gel for the treatment of rheumatoid arthritis. The fabricated transfersomes showed promising therapeutic outcomes in terms of behavioral findings, arthritic index, and histological findings. The study also showed improvement in the expression of Nrf2 and HO-1 proteins, suggesting an improvement in the arthritic condition.
Rheumatoid arthritis restricts the physical ability of patients and increases the disease burden; therefore, research has always been focused on evaluating better therapeutic options. The present research aimed to design Continentalic acid (CA)-loaded transfersomes (CA-TF) embedded in Carbopol gel containing permeation enhancer ( PE) for the treatment of rheumatoid arthritis. CA-TF was developed via a modified thin film hydration method and incorporated into Carbopol 934 gel containing Eucalyptus oil (EO) as PE. The fabricated CA-TF showed particle size of < 140 nm with spherical geometry, optimal encapsulation efficiency (EE), and sustained drug release pattern. CA-TF-gel along with PE (CA-TF-PE-gel) showed better ex vivo skin penetration than plain CA gel and CA-TF-gel without PE. In vivo evaluation supported improved therapeutic outcomes of CA-TF-PE-gel in terms of behavioral findings, arthritic index, and histological findings whereas biochemical assays and pro-inflammatory cytokines (TNF-alpha and IL-1 beta) showed a significant decrease in their levels. Furthermore, immunohistochemistry assay for Nrf2 and HO-1 signaling pathways showed significant improvement in the expression of the Nrf2, and HO-1 proteins to depict improvement in arthritic condition in the animal model. CA-TF-PE-gel significantly delivered CA to the diseased target site via a topical route with promising therapeutic outcomes displayed in the CFA-induced arthritic model.

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