ArticleNaunyn-Schmiedeberg's archives of pharmacology2026
QbD-enabled leflunomide-transfersomal gel for topical treatment of rheumatoid arthritis.
Article in Naunyn-Schmiedeberg's archives of pharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Authors and funding
6 authors.
Funding
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Abstract
This study aimed to create innovative transfersomes (TRFs) consisting of a lipid blend and a chemical permeation enhancer for efficient transdermal delivery of leflunomide (LFN). Leflunomide, a dihydroorotate dehydrogenase inhibitor, is mainly used to manage rheumatoid arthritis (RA). Oral consumption of LFN for RA can lead to adverse systemic effects; hence, local application is advisable. To develop topical dosage form of LFN, transfersomes with improved skin permeation capabilities were fabricated. The vesicle diameter of LFN-TRF was determined to be 181.2 ± 2.17 nm, zeta potential of - 29.2 ± 0.06 mV, PDI of 0.259 ± 0.006, and encapsulation percentage (EE) of 86.5 ± 3.45%. Notably, the developed formulation exhibited slow and sustained release of up to 78.87% of LFN over 24 h. The drug permeation from the nanocarriers was found to be around 67% for the LFN-TRF-gel and 55.33% for the LFN-gel. Skin irritation assessments indicated no signs of irritation, inflammation, or toxicity, affirming the formulation's nontoxic and biocompatible characteristics. In vivo studies demonstrated higher anti-inflammatory and anti-arthritic activity than conventional gel. In summary, this study presents a viable alternative for formulating effective topical LFN preparation using transfersomes.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.