Aksungur Pelin, Sungur Arzu, Unal Serhat, Iskit Alper B, Squier Christopher A, Senel Sevda
Department of Pharmaceutical Technology, Faculty of Pharmacy, Hacettepe University, Ankara 06100, Turkey.
J Control Release. 2004 Aug 11;98(2):269-79. doi: 10.1016/j.jconrel.2004.05.002.
Oral mucositis is a frequent and potentially severe complication of radiation or chemotherapy for cancer. Associated with atrophy and ulceration of the oral mucosa is an increased risk of infection, and the most common pathogenic agent is Candida. Chitosan is an excellent candidate for the treatment of oral mucositis. Its bioadhesive and antimicrobial properties offer the palliative effects of an occlusive dressing and the potential for delivering drugs, including anti-candidal agents. The aim of this study was to develop an occlusive bioadhesive system for prophylaxis and/or treatment of oral mucositis. Gel and film formulations were prepared using chitosans at different molecular weights and in different solvents. Nystatin, which is considered as a prophylactic agent for oral mucositis was incorporated into the formulations. The in vitro release of nystatin from the formulations was decreased with the increasing molecular weight of chitosan. The effect of the formulations was investigated in vivo in hamsters with chemotherapy-induced mucositis. Mucositis scores in groups treated with nystatin incorporated into gel and suspension formulations were significantly lower (p < 0.05) than those treated with the chitosan gel alone. Survival of animals in the treated groups was higher than that in the control group. The retention time and distribution of the gels in the oral cavity were investigated in healthy volunteers. A faster distribution of nystatin in the oral cavity was obtained using the suspension compared to the gels, but the nystatin saliva level decreased rapidly as well. A drug concentration above the minimum inhibitory concentration (MIC) value for Candida albicans (0.14 microg/ml) was maintained for longer periods of time at the application site (90 min) than at the contralateral site (45 min) in the oral cavity.
口腔黏膜炎是癌症放疗或化疗常见且可能严重的并发症。口腔黏膜萎缩和溃疡会增加感染风险,最常见的病原体是念珠菌。壳聚糖是治疗口腔黏膜炎的理想选择。其生物黏附性和抗菌特性兼具封闭敷料的缓解作用以及递送药物(包括抗念珠菌剂)的潜力。本研究的目的是开发一种用于预防和/或治疗口腔黏膜炎的封闭性生物黏附系统。使用不同分子量的壳聚糖在不同溶剂中制备凝胶和薄膜制剂。将被视为口腔黏膜炎预防剂的制霉菌素加入制剂中。制霉菌素从制剂中的体外释放随着壳聚糖分子量的增加而降低。在化疗诱导的黏膜炎仓鼠体内研究了制剂的效果。用加入制霉菌素的凝胶和混悬液制剂治疗的组的黏膜炎评分显著低于单独使用壳聚糖凝胶治疗的组(p < 0.05)。治疗组动物的存活率高于对照组。在健康志愿者中研究了凝胶在口腔中的保留时间和分布。与凝胶相比,使用混悬液时制霉菌素在口腔中的分布更快,但制霉菌素唾液水平也迅速下降。在口腔中,在应用部位(90分钟)保持白色念珠菌最低抑菌浓度(MIC)值(0.14微克/毫升)以上的药物浓度的时间比在对侧部位(45分钟)更长。