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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.
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http://dx.doi.org/10.1016/j.ijpharm.2024.124829 | DOI Listing |
Drug Dev Res
September 2025
Department of Pharmaceutics, School of Pharmacy, Center for Nano Drug/Gene Delivery and Tissue Engineering, Jiangsu Provincial Research Center for Medicinal Function Development of New Food Resources, Jiangsu University, Zhenjiang, Jiangsu, China.
Liver cancer is the fourth most deadly cancer worldwide, but existing treatment options are insufficient, thus highlighting the urgent need for new therapeutic agents. Taxanes, known for their anticancer properties, provide a promising avenue for intervention. In this study, a tetracyclic taxane compound with antitumor activity (taxinine) was extracted and isolated from Taxus chinensis (T.
View Article and Find Full Text PDFJ Drug Target
September 2025
Department of Pharmaceutics, Division of Pharmaceutical Sciences, College of Pharmacy, Arab Academy for Science, Technology and Maritime Transport, Alexandria, P.O. Box 1029, Egypt.
Rheumatoid arthritis (RA) is a chronic autoimmune disease that causes joint inflammation, cartilage deterioration, and oxidative stress. The study developed transdermal RA treatment with L-carnosine (CAR)-loaded chondroitin sulfate (CHS) functionalized proposomes. CHS-functionalized proposomes measured 285 ± 0.
View Article and Find Full Text PDFJ Control Release
August 2025
Department of Biochemistry and Molecular Biology, School of Life Sciences, Central South University, Changsha, Hunan Province 410078, China. Electronic address:
Spinal cord injury (SCI) often results in irreversible neurological deficits, primarily due to chronic neuroinflammation driven by activated proinflammatory microglia. Effective therapeutic interventions require both precise targeting of pathological immune cells and sustained modulation of the inflammatory microenvironment. Here, we present a cell specific, hydrogel-based nanoparticle system (MG1-MM@Candesartan-Gel) designed for the selective and prolonged delivery of the angiotensin II type 1 receptor (AT1R) antagonist Candesartan to proinflammatory microglia.
View Article and Find Full Text PDFAAPS PharmSciTech
August 2025
Department of Industrial Pharmacy and Quality Assurance, R.C. Patel Institute of Pharmaceutical Education and Research, Shirpur, 425405, India.
Stiripentol (STP), an antiepileptic drug, is administered orally in the form of capsule and dry suspension. However, it is extremely unstable in acidic environment. Hence, to find the feasibility of alternate route of administration and to enhance the bioavailability of drug, STP loaded intranasal in-situ nanolipoidal gel formulation was formulated.
View Article and Find Full Text PDFFood Chem
August 2025
College of Food Science and Technology, Bohai University, Jinzhou, 121013, China; Liaoning Province Key Laboratory for Emission Reduction, Efficiency Improvement and Comprehensive Utilization of Agricultural Products, Jinzhou 121013, China.
Soybean protein isolate (SPI) and soy hull polysaccharide (SHP) were combined with lutein liposomes (Lu-lip) to form an SPI-SHP lutein liposome gel (SPI-SHP Lu-lip gel) through dual-induced cross-linking using Ca and TGase. With increasing SHP concentration, the formation of a stable composite gel structure resulted in a gradual improvement in the water-holding capacity (WHC) of the SPI-SHP Lu-lip gels. At 3.
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