Topical Melatonin Niosome Gel for the Treatment of 5-FU-Induced Oral Mucositis in Mice

粘膜炎 医学 褪黑素 丙二醛 口服 牙周炎 药理学 氧化应激 尼奥体 抗氧化剂 促炎细胞因子 氟辛醇酮 胃肠病学 炎症 内科学 消炎药 脂质过氧化 牙龈炎 口炎 生物利用度 肿瘤坏死因子α 细胞因子
作者
Prangtip Uthaiwat,Jureerut Daduang,Aroonsri Priprem,Chatri Settasatian,Sirinart Chio‐Srichan,Yao-Chang Lee,Pramote Mahakunakorn,Patcharee Boonsiri
出处
期刊:Current Drug Delivery [Bentham Science Publishers]
卷期号:18 (2): 199-211 被引量:14
标识
DOI:10.2174/1567201817666200525151848
摘要

Background: Oral mucositis, one of the most common complications of 5-Fluorouracil (5-FU) treatment, leads to several problems, including pain, diarrhea and malnutrition, and reduces the quality of life and subsequent treatments. Melatonin, a neurohormone with anti-inflammatory and antioxidant activities, was encapsulated in niosomes and embedded in a mucoadhesive gel formulation as a Melatonin Niosome Gel (MNG) to perform oral mucositis treatment. Objective: This study aimed to investigate the effectiveness of MNG for the treatment of 5-FU-induced oral mucositis in mice. Methods: Oral mucositis was induced in ICR mice by 5-FU and randomly assigned to receive daily applications of the topical oral MNG, a fluocinolone acetonide gel, a blank niosome gel, or no treatment for 5 days in comparison with a normal group. Average body weights, food consumption, and behaviors of the mice as well as microscopic histopathology, Fourier-Transform Infrared Spectroscopy (FTIR) analysis, proinflammatory cytokine levels, and oxidative stress markers of the tongues were monitored and collected after sacrifice. Results: In comparison to the normal group, the average body weights of the 5-FU-MNG mice did not deviate from that of the normal group, nor was there a significant difference in the time to sleep or licking ( p >0.05 for both parameters). In addition, the mice treated with MNG and fluocinolone acetonide did not show significantly different histopathological, FTIR, interleukin-1β or malondialdehyde (MDA) results in the tongues used as the oral tissue samples. Conclusion: Topical MNG potentially inhibits inflammation and lipid oxidative stress in 5-FU-induced oral mucositis.
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