Omega-3-and Resveratrol-Loaded Lipid Nanosystems for Potential Use as Topical Formulations in Autoimmune, Inflammatory, and Cancerous Skin Diseases

被引:17
|
作者
Caldas, Ana R. [1 ]
Catita, Jose [2 ,3 ,4 ]
Machado, Raul [5 ,6 ]
Ribeiro, Artur [7 ]
Cerqueira, Fatima [2 ,3 ,8 ,9 ]
Horta, Bruno [9 ,10 ,11 ]
Medeiros, Rui [2 ,3 ,9 ,11 ]
Lucio, Marlene [1 ,5 ]
Lopes, Carla M. [2 ,3 ]
机构
[1] Univ Minho, Dept Fis, CF UM UP, P-4710057 Braga, Portugal
[2] Biomed Res Ctr FP ENAS CEBIMED, Fernando Pessoa Energy Environm & Hlth Res Unit, FP I3ID, P-4200150 Porto, Portugal
[3] Fernando Pessoa Univ, Fac Hlth Sci, P-4200150 Porto, Portugal
[4] Paralab SA, P-4420392 Valbom, Portugal
[5] Univ Minho, Dept Biol, CBMA, P-4710057 Braga, Portugal
[6] Univ Minho, IB S Inst Sci & Innovat Biosustainabil, Campus Gualtar, P-4710057 Braga, Portugal
[7] Univ Minho, CEB, P-4710057 Braga, Portugal
[8] Interdisciplinary Ctr Marine & Environm Res, CIIMAR CIMAR, P-4450208 Matosinhos, Portugal
[9] Portuguese Oncol Inst Porto IPO Porto, Porto Comprehens Canc Ctr Porto CCC, RISE CI IPOP Hlth Res Network, Mol Oncol & Viral Pathol Grp,Res Ctr IPO Porto CI, P-4200072 Porto, Portugal
[10] Portuguese Catholic Univ, Higher Sch Biotechnol, Associated Lab, CBQF Ctr Biotechnol & Fine Chem, P-4169005 Porto, Portugal
[11] Univ Porto, ICBAS Inst Ciencias Biomed Abel Salazar, P-4050313 Porto, Portugal
关键词
resveratrol; omega; 3; topical skin administration; lipid nanosystems; COX inhibitors; NO inhibitory effect; antioxidant; POLYUNSATURATED FATTY-ACIDS; NITRIC-OXIDE PRODUCTION; TRANS-RESVERATROL; DRUG-DELIVERY; CARRIERS NLC; IN-VITRO; NANOPARTICLES; LIPOSOMES; OMEGA-3-FATTY-ACIDS; PSORIASIS;
D O I
10.3390/pharmaceutics13081202
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Resveratrol (RSV) and omega 3 (omega(3)), because of their biological favorable properties, have become subjects of interest for researchers in dermocosmetic and pharmaceutical industries; however, these bioactives present technological limitations that hinder their effective delivery to the target skin layer. To overcome the stability and skin permeation limitations of free bioactives, this work proposes a combined strategy involving two different lipid nanosystems (liposomes and lipid nanoparticles) that include omega(3) in their lipid matrix. Additionaly, RSV is only encapsulated in liposomes that provid an adequate amphiphilic environment. Each formulation is thoroughly characterized regarding their physical-chemical properties. Subsequently, the therapeutic performance of the lipid nanosystems is evaluated based on their protective roles against lipid peroxidation, as well as inhibition of cicloxygenase (COX) and nitric oxid (NO) production in the RWA264.7 cell line. Finally, the lipid nanosystems are incorporated in hydrogel to allow their topical administration, then rheology, occlusion, and RSV release-diffusion assays are performed. Lipid nanoparticles provide occlusive effects at the skin surface. Liposomes provide sustained RSV release and their flexibility conferred by edge activator components enhances RSV diffusion, which is required to reach NO production cells and COX cell membrane enzymes. Overall, the inclusion of both lipid nanosystems in the same semisolid base constitutes a promising strategy for autoimmune, inflammatory, and cancerous skin diseases.
引用
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页数:22
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