Treating atopic-dermatitis-like skin lesions in mice with gelatin-alginate films containing 1,4-anhydro-4-seleno-D-talitol (SeTal)

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

Treating atopic-dermatitis-like skin lesions in mice with gelatin-alginate films containing 1,4-anhydro-4-seleno-D-talitol (SeTal). / Voss, Guilherme T.; Davies, Michael J.; Schiesser, Carl H.; de Oliveira, Renata L.; Nornberg, Andresa B.; Soares, Victória R.; Barcellos, Angelita M.; Luchese, Cristiane; Fajardo, André R.; Wilhelm, Ethel A.

In: International Journal of Pharmaceutics, Vol. 642, 123174, 2023.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Voss, GT, Davies, MJ, Schiesser, CH, de Oliveira, RL, Nornberg, AB, Soares, VR, Barcellos, AM, Luchese, C, Fajardo, AR & Wilhelm, EA 2023, 'Treating atopic-dermatitis-like skin lesions in mice with gelatin-alginate films containing 1,4-anhydro-4-seleno-D-talitol (SeTal)', International Journal of Pharmaceutics, vol. 642, 123174. https://doi.org/10.1016/j.ijpharm.2023.123174

APA

Voss, G. T., Davies, M. J., Schiesser, C. H., de Oliveira, R. L., Nornberg, A. B., Soares, V. R., Barcellos, A. M., Luchese, C., Fajardo, A. R., & Wilhelm, E. A. (2023). Treating atopic-dermatitis-like skin lesions in mice with gelatin-alginate films containing 1,4-anhydro-4-seleno-D-talitol (SeTal). International Journal of Pharmaceutics, 642, [123174]. https://doi.org/10.1016/j.ijpharm.2023.123174

Vancouver

Voss GT, Davies MJ, Schiesser CH, de Oliveira RL, Nornberg AB, Soares VR et al. Treating atopic-dermatitis-like skin lesions in mice with gelatin-alginate films containing 1,4-anhydro-4-seleno-D-talitol (SeTal). International Journal of Pharmaceutics. 2023;642. 123174. https://doi.org/10.1016/j.ijpharm.2023.123174

Author

Voss, Guilherme T. ; Davies, Michael J. ; Schiesser, Carl H. ; de Oliveira, Renata L. ; Nornberg, Andresa B. ; Soares, Victória R. ; Barcellos, Angelita M. ; Luchese, Cristiane ; Fajardo, André R. ; Wilhelm, Ethel A. / Treating atopic-dermatitis-like skin lesions in mice with gelatin-alginate films containing 1,4-anhydro-4-seleno-D-talitol (SeTal). In: International Journal of Pharmaceutics. 2023 ; Vol. 642.

Bibtex

@article{e3a81abed17f403d9469fdd8e579ea47,
title = "Treating atopic-dermatitis-like skin lesions in mice with gelatin-alginate films containing 1,4-anhydro-4-seleno-D-talitol (SeTal)",
abstract = "New compounds and pharmacological strategies offer alternatives for treating chronic skin diseases, such as atopic dermatitis (AD). Here, we investigated the incorporation of 1,4-anhydro-4-seleno-D-talitol (SeTal), a bioactive seleno-organic compound, in gelatin and alginate (Gel-Alg) polymeric films as a strategy for improving the treatment and attenuation of AD-like symptoms in a mice model. Hydrocortisone (HC) or vitamin C (VitC) were incorporated with SeTal in the Gel-Alg films, and their synergy was investigated. All the prepared film samples were able to retain and release SeTal in a controlled manner. In addition, appreciable film handling facilitates SeTal administration. A series of in-vivo/ex-vivo experiments were performed using mice sensitized with dinitrochlorobenzene (DNCB), which induces AD-like symptoms. Long-term topical application of the loaded Gel-Alg films attenuated disease symptoms and pruritus, with suppression of the levels of inflammatory markers, oxidative damage, and the skin lesions associated with AD. Moreover, the loaded films showed superior efficiency in attenuating the analyzed symptoms when compared to hydrocortisone (HC) cream, a traditional AD-treatment, and decreased the inherent drawbacks of this compound. In short, incorporating SeTal (by itself or with HC or VitC) in biopolymeric films provides a promising alternative for the long-term treatment of AD-type skin diseases.",
keywords = "1,4-anhydro-4-seleno-D-talitol, Biomaterials, Drug delivery, Hydrocortisone, Skin diseases, vitamin C",
author = "Voss, {Guilherme T.} and Davies, {Michael J.} and Schiesser, {Carl H.} and {de Oliveira}, {Renata L.} and Nornberg, {Andresa B.} and Soares, {Vict{\'o}ria R.} and Barcellos, {Angelita M.} and Cristiane Luchese and Fajardo, {Andr{\'e} R.} and Wilhelm, {Ethel A.}",
note = "Publisher Copyright: {\textcopyright} 2023 Elsevier B.V.",
year = "2023",
doi = "10.1016/j.ijpharm.2023.123174",
language = "English",
volume = "642",
journal = "International Journal of Pharmaceutics",
issn = "0378-5173",
publisher = "Elsevier",

}

RIS

TY - JOUR

T1 - Treating atopic-dermatitis-like skin lesions in mice with gelatin-alginate films containing 1,4-anhydro-4-seleno-D-talitol (SeTal)

AU - Voss, Guilherme T.

AU - Davies, Michael J.

AU - Schiesser, Carl H.

AU - de Oliveira, Renata L.

AU - Nornberg, Andresa B.

AU - Soares, Victória R.

AU - Barcellos, Angelita M.

AU - Luchese, Cristiane

AU - Fajardo, André R.

AU - Wilhelm, Ethel A.

N1 - Publisher Copyright: © 2023 Elsevier B.V.

PY - 2023

Y1 - 2023

N2 - New compounds and pharmacological strategies offer alternatives for treating chronic skin diseases, such as atopic dermatitis (AD). Here, we investigated the incorporation of 1,4-anhydro-4-seleno-D-talitol (SeTal), a bioactive seleno-organic compound, in gelatin and alginate (Gel-Alg) polymeric films as a strategy for improving the treatment and attenuation of AD-like symptoms in a mice model. Hydrocortisone (HC) or vitamin C (VitC) were incorporated with SeTal in the Gel-Alg films, and their synergy was investigated. All the prepared film samples were able to retain and release SeTal in a controlled manner. In addition, appreciable film handling facilitates SeTal administration. A series of in-vivo/ex-vivo experiments were performed using mice sensitized with dinitrochlorobenzene (DNCB), which induces AD-like symptoms. Long-term topical application of the loaded Gel-Alg films attenuated disease symptoms and pruritus, with suppression of the levels of inflammatory markers, oxidative damage, and the skin lesions associated with AD. Moreover, the loaded films showed superior efficiency in attenuating the analyzed symptoms when compared to hydrocortisone (HC) cream, a traditional AD-treatment, and decreased the inherent drawbacks of this compound. In short, incorporating SeTal (by itself or with HC or VitC) in biopolymeric films provides a promising alternative for the long-term treatment of AD-type skin diseases.

AB - New compounds and pharmacological strategies offer alternatives for treating chronic skin diseases, such as atopic dermatitis (AD). Here, we investigated the incorporation of 1,4-anhydro-4-seleno-D-talitol (SeTal), a bioactive seleno-organic compound, in gelatin and alginate (Gel-Alg) polymeric films as a strategy for improving the treatment and attenuation of AD-like symptoms in a mice model. Hydrocortisone (HC) or vitamin C (VitC) were incorporated with SeTal in the Gel-Alg films, and their synergy was investigated. All the prepared film samples were able to retain and release SeTal in a controlled manner. In addition, appreciable film handling facilitates SeTal administration. A series of in-vivo/ex-vivo experiments were performed using mice sensitized with dinitrochlorobenzene (DNCB), which induces AD-like symptoms. Long-term topical application of the loaded Gel-Alg films attenuated disease symptoms and pruritus, with suppression of the levels of inflammatory markers, oxidative damage, and the skin lesions associated with AD. Moreover, the loaded films showed superior efficiency in attenuating the analyzed symptoms when compared to hydrocortisone (HC) cream, a traditional AD-treatment, and decreased the inherent drawbacks of this compound. In short, incorporating SeTal (by itself or with HC or VitC) in biopolymeric films provides a promising alternative for the long-term treatment of AD-type skin diseases.

KW - 1,4-anhydro-4-seleno-D-talitol

KW - Biomaterials

KW - Drug delivery

KW - Hydrocortisone

KW - Skin diseases

KW - vitamin C

UR - http://www.scopus.com/inward/record.url?scp=85163879555&partnerID=8YFLogxK

U2 - 10.1016/j.ijpharm.2023.123174

DO - 10.1016/j.ijpharm.2023.123174

M3 - Journal article

C2 - 37364783

AN - SCOPUS:85163879555

VL - 642

JO - International Journal of Pharmaceutics

JF - International Journal of Pharmaceutics

SN - 0378-5173

M1 - 123174

ER -

ID: 360070264