Chondroitin Sulfate for cartilage regeneration, administered topically using a nanostructured formulation

dc.contributor.authorBustos Araya, Marta Eduviges
dc.contributor.authorNardi Ricart, Anna
dc.contributor.authorCalpena Campmany, Ana Cristina
dc.contributor.authorMiñarro Carmona, Montserrat
dc.date.accessioned2024-10-25T09:43:18Z
dc.date.available2024-10-25T09:43:18Z
dc.date.issued2024-09-18
dc.date.updated2024-10-25T09:43:18Z
dc.description.abstractIn the pharmaceutical sector, solid lipid nanoparticles (SLN) are vital for drug delivery incorporating a lipid core. Chondroitin sulfate (CHON) is crucial for cartilage health. It is often used in osteoarthritis (OA) treatment. Due to conflicting results from clinical trials on CHON’s efficacy in OA treatment, there has been a shift toward exploring effective topical systems utilizing nanotechnology. This study aimed to optimize a solid lipid nanoparticle formulation aiming to enhance CHON permeation for OA therapy. A 3 × 3 × 2 Design of these experiments determined the ideal parameters: a CHON concentration of 0.4 mg/mL, operating at 20,000 rpm speed, and processing for 10 min for SLN production. Transmission electron microscopy analysis confirmed the nanoparticles’ spherical morphology, ensuring crucial uniformity for efficient drug delivery. Cell viability assessments showed no significant cytotoxicity within the tested parameters, indicating a safe profile for potential clinical application. The cell internalization assay indicates successful internalization at 1.5 h and 24 h post-treatment. Biopharmaceutical studies supported SLNs, indicating them to be effective CHON carriers through the skin, showcasing improved skin permeation and CHON retention compared to conventional methods. In summary, this study successfully optimized SLN formulation for efficient CHON transport through pig ear skin with no cellular toxicity, highlighting SLNs’ potential as promising carriers to enhance CHON delivery in OA treatment and advance nanotechnology-based therapeutic strategies in pharmaceutical formulations. Keywords: solid lipid nanoparticles; chondroitin sulfate; osteoarthritis; skin permeation; design of experiments; cell viability; biopharmaceutical studies; drug delivery
dc.format.extent1 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec750956
dc.identifier.issn1661-6596
dc.identifier.urihttps://hdl.handle.net/2445/216039
dc.language.isoeng
dc.publisherMDPI
dc.relation.isformatofReproducció del document publicat a: https://doi.org/doi.org/10.3390/ijms251810023
dc.relation.ispartofInternational Journal of Molecular Sciences, 2024, vol. 25, num.18
dc.relation.urihttps://doi.org/doi.org/10.3390/ijms251810023
dc.rightscc-by (c) Marta E. Bustos Araya et al., 2024
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceArticles publicats en revistes (Farmàcia, Tecnologia Farmacèutica i Fisicoquímica)
dc.subject.classificationNanopartícules
dc.subject.classificationNanotecnologia
dc.subject.classificationArtrosi
dc.subject.otherNanoparticles
dc.subject.otherNanotechnology
dc.subject.otherOsteoarthritis
dc.titleChondroitin Sulfate for cartilage regeneration, administered topically using a nanostructured formulation
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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