Chondroitin Sulfate for Cartilage Regeneration, Administered Topically Using a Nanostructured Formulation

被引:1
|
作者
Bustos Araya, Marta E. [1 ]
Nardi-Ricart, Anna [2 ]
Calpena Capmany, Ana C. [2 ,3 ]
Minarro Carmona, Montserrat [2 ,4 ]
机构
[1] Univ Costa Rica, Fac Farm, Inst Invest Farmaceut, San Jose 11501, Costa Rica
[2] Univ Barcelona, Pharm Pharmaceut Technol & Physicochem Dept, Ave Joan XXIII 27-31, Barcelona 08028, Spain
[3] Univ Barcelona, Inst Nanosci & Nanotechnol IN2UB, Barcelona 08028, Spain
[4] IDIBELL UB Res Grp, Pharmacotherapy Pharmacogen & Pharmaceut Technol, Avinguda Granvia 199-203, LHosp De Llobregat 08908, Spain
关键词
solid lipid nanoparticles; chondroitin sulfate; osteoarthritis; skin permeation; design of experiments; cell viability; biopharmaceutical studies; drug delivery; SOLID LIPID NANOPARTICLES; CARRIERS; OSTEOARTHRITIS;
D O I
10.3390/ijms251810023
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In 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 x 3 x 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.
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页数:19
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