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J Nanobiotechnology ; 22(1): 51, 2024 Feb 06.
Artigo em Inglês | MEDLINE | ID: mdl-38321547

RESUMO

BACKGROUND: Allergic rhinitis (AR) is a prevalent immune-related allergic disease, and corticosteroid nasal sprays serve as the primary treatment for this patient population. However, their short duration of efficacy and frequent administration pose challenges, leading to drug wastage and potential adverse effects. To overcome these limitations, we devised a novel approach to formulate DEX-Gel by incorporating dexamethasone (DEX) into a blend of Pluronic F127, stearic acid (SA), and polyethylene glycol 400 (PEG400) to achieve sustained-release treatment for AR. RESULTS: Following endoscopic injection into the nasal mucosa of AR rats, DEX-Gel exhibited sustained release over a 14-day period. In vivo trials employing various assays, such as flow cytometry (FC), demonstrated that DEX-Gel not only effectively managed allergic symptoms but also significantly downregulated helper T-cells (TH) 2 and TH2-type inflammatory cytokines (e.g., interleukins 4, 5, and 13). Additionally, the TH1/TH2 cell ratio was increased. CONCLUSION: This innovative long-acting anti-inflammatory sustained-release therapy addresses the TH1/TH2 immune imbalance, offering a promising and valuable approach for the treatment of AR and other inflammatory nasal diseases.


Assuntos
Rinite Alérgica , Células Th1 , Humanos , Ratos , Animais , Camundongos , Preparações de Ação Retardada/farmacologia , Células Th2 , Rinite Alérgica/tratamento farmacológico , Citocinas , Anti-Inflamatórios/farmacologia , Modelos Animais de Doenças , Ovalbumina , Camundongos Endogâmicos BALB C
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