De Grau, Guillermo
Mallandrich Miret, Mireia
Sosa Díaz, Lilian Elisa
Espinoza, Lupe Carolina
Calpena Campmany, Ana Cristina
Bozal de Febrer, Núria
Rodríguez Allué, Manuel José
Garduño Ramírez, María Luisa del Carmen
Rincón, María
2025-01-27T11:15:06Z
2025-01-27T11:15:06Z
2024-05
2025-01-27T11:15:06Z
Recently, the number of people acquiring tattoos has increased, with tattoos gaining significant popularity in people between 20 and 40 years old. Inflammation is a common reaction associated with tattooing. The purpose of this study was to evaluate a nanostructured lipid carrier loading pranoprofen (PRA-NLC) as a tattoo aftercare formulation to reduce the inflammation associated with tattooing. In this context, the in vitro drug release and the ex vivo permeation-through-human-skin tests using Franz cells were appraised. The tolerance of our formulation on the skin was evaluated by studying the skin’s biomechanical properties. In addition, an in vivo anti-inflammatory study was conducted on mice skin to evaluate the efficacy of the formulation applied topically after tattooing the animals. PRA-NLC showed a sustained release up to 72 h, and the amount of pranoprofen retained in the skin was found to be 33.48 µg/g/cm2. The formulation proved to be well tolerated; it increased stratum corneum hydration, and no signs of skin irritation were observed. Furthermore, it was demonstrated to be non-cytotoxic since the cell viability was greater than 80%. Based on these results, we concluded that PRA-NLC represents a suitable drug delivery carrier for the transdermal delivery of pranoprofen to alleviate the local skin inflammation associated with tattooing.
English
Malalties de la pell; Lípids; Nanopartícules; Tatuatges; Skin diseases; Lipids; Nanoparticles; Tattooing
MDPI
Reproducció del document publicat a: https://doi.org/https://doi.org/10.3390/pharmaceutics16050643
Pharmaceutics, 2024, vol. 16, num.5, p. 643
https://doi.org/https://doi.org/10.3390/pharmaceutics16050643
cc-by (c) De Grau, G. et al., 2024
http://creativecommons.org/licenses/by/4.0/