Fabrication and Evaluation of Rimantadine Loaded Niosomes

S. P, Alagarsamy V, Subhash Chandra Bose P., S. V, Saritha D
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Abstract

Influenza virus is a highly contagious zoonotic respiratory disease that causes seasonal outbreaks each year and unpredictable pandemics occasionally with high morbidity and mortality rates, posing a great threat to public health worldwide. Besides the limited effect of vaccines, the problem is exacerbated by the lack of drugs with strong antiviral activity against all flu strains. Rimantadine is one of the effective anti-viral drugs that is used in treating influenza virus. In present study niosomes of Rimantadine were developed by ether injection method. Total 6 formulations were prepared by altering ratios of span 60 and cholesterol. The prepared formulations were evaluated for different parameters. In vitro drug release studies were carried out for all the formulations and among five formulations F5 was found to have highest drug release. Prepared niosomes were incorporated in gel and evaluation studies like pH, homogenicity, viscosity and spreadability were carried out. All the parameters were found satisfactory. It was compared with marketed gel. The former has shown drug release till 12 h whereas the latter has shown only till 6 h. Thus, sustained release of drug loaded niosomes was proved.
金刚乙胺负载牛小体的制备与评价
流感病毒是一种高度传染性的人畜共患呼吸道疾病,每年都会引起季节性疫情,偶尔会出现不可预测的大流行,发病率和死亡率都很高,对全世界的公共卫生构成巨大威胁。除了疫苗的作用有限之外,缺乏对所有流感病毒株都具有强抗病毒活性的药物使问题更加严重。金刚乙胺是一种有效的抗病毒药物,用于治疗流感病毒。本研究采用乙醚注射法制备了金刚乙胺小体。通过改变span - 60与胆固醇的比例,共制得6种配方。对制备的配方进行了不同参数的评价。对所有制剂进行体外释药研究,发现5种制剂中F5释药最高。将制备好的乳质体掺入凝胶中,并进行pH、均质性、粘度和铺展性等评价研究。所有参数均令人满意。并与市售凝胶进行了比较。前者的药物释放时间为12小时,而后者仅为6小时。因此,证明了载药小体的缓释作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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