TY - JOUR
T1 - Topical nitric oxide releasing nanoparticles are effective in a murine model of dermal Trichophyton rubrum dermatophytosis
AU - Mordorski, Breanne
AU - Costa-Orlandi, Caroline Barcelos
AU - Baltazar, Ludmila M.
AU - Carreño, Leandro J.
AU - Landriscina, Angelo
AU - Rosen, Jamie
AU - Navati, Mahantesh
AU - Mendes-Giannini, Maria Jose Soares
AU - Friedman, Joel M.
AU - Nosanchuk, Joshua D.
AU - Friedman, Adam J.
N1 - Funding Information:
Funding: CBCO received fellowship funding from Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (process number: 99999.007910/2014-02) and Conselho Nacional de Desenvolvimento Científico e Tecnológico (process number: 150261/2016-0).
Publisher Copyright:
© 2017 Elsevier Inc.
PY - 2017/10
Y1 - 2017/10
N2 - Systemic therapies are preferred for treating dermal dermatophytosis due to inadequate penetration of topical agents. However, systemic antifungals are associated with off-target effects and limited tissue penetration, and antimicrobial resistance is a growing concern. To address this, we investigated topical nitric oxide-releasing nanoparticles (NO-np), which have been used against superficial fungal infections and bacterial abscesses. In addition to enhanced penetration and permeation conferred by nanoparticles, nitric oxide, a broad-spectrum multi-mechanistic antimicrobial agent, offers decreased likelihood of resistance development. In the current study, NO-np inhibited Trichophyton rubrum in vitro, as well as in a murine model of dermal dermatophytosis. In mice, NO-np reduced fungal burden after three days, with complete clearance after seven. Furthermore, NO-np decreased tissue IL-2, 6, 10 and TNFα, indicating earlier attenuation of the host inflammatory response and decreased tissue morbidity. Thus, topical NO-np represent an attractive alternative to systemic therapy against dermal T. rubrum infection.
AB - Systemic therapies are preferred for treating dermal dermatophytosis due to inadequate penetration of topical agents. However, systemic antifungals are associated with off-target effects and limited tissue penetration, and antimicrobial resistance is a growing concern. To address this, we investigated topical nitric oxide-releasing nanoparticles (NO-np), which have been used against superficial fungal infections and bacterial abscesses. In addition to enhanced penetration and permeation conferred by nanoparticles, nitric oxide, a broad-spectrum multi-mechanistic antimicrobial agent, offers decreased likelihood of resistance development. In the current study, NO-np inhibited Trichophyton rubrum in vitro, as well as in a murine model of dermal dermatophytosis. In mice, NO-np reduced fungal burden after three days, with complete clearance after seven. Furthermore, NO-np decreased tissue IL-2, 6, 10 and TNFα, indicating earlier attenuation of the host inflammatory response and decreased tissue morbidity. Thus, topical NO-np represent an attractive alternative to systemic therapy against dermal T. rubrum infection.
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U2 - 10.1016/j.nano.2017.06.018
DO - 10.1016/j.nano.2017.06.018
M3 - Article
C2 - 28712918
AN - SCOPUS:85026456792
SN - 1549-9634
VL - 13
SP - 2267
EP - 2270
JO - Nanomedicine: Nanotechnology, Biology, and Medicine
JF - Nanomedicine: Nanotechnology, Biology, and Medicine
IS - 7
ER -