首页> 美国卫生研究院文献>Iranian Journal of Pharmaceutical Research : IJPR >Efficacy and Physicochemical Evaluation of an Optimized Semisolid Formulation of Povidone Iodine Proposed by Extreme Vertices Statistical Design; a Practical Approach
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Efficacy and Physicochemical Evaluation of an Optimized Semisolid Formulation of Povidone Iodine Proposed by Extreme Vertices Statistical Design; a Practical Approach

机译:极点统计设计提出的聚维酮碘最佳半固体配方的功效和理化评价;实用的方法

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摘要

One of the most significant issues in pharmaceutical industries, prior to commercialization of a pharmaceutical preparation is the "preformulation" stage. However, far too attention has been paid to verification of the software assisted statistical designs in preformulation studies. The main aim of this study was to report a step by step preformulation approach for a semisolid preparation based on a statistical mixture design and to verify the predictions made by the software with an in-vitro efficacy bioassay test. Extreme vertices mixture design (4 factors, 4 levels) was applied for preformulation of a semisolid Povidone Iodine preparation as Water removable ointment using different PolyEthylenGlycoles. Software Assisted (Minitab) analysis was then performed using four practically assessed response values including; Available iodine, viscosity (N index and yield value) and water absorption capacity. Subsequently mixture analysis was performed and finally, an optimized formulation was proposed. The efficacy of this formulation was bio-assayed using microbial tests in-vitro and MIC values were calculated for Escherichia coli, pseudomonaaeruginosa, staphylococcus aureus and Candida albicans.Results indicated the acceptable conformity of the measured responses. Thus, it can be concluded that the proposed design had an adequate power to predict the responses in practice. Stability studies, proved no significant change during the one year study for the optimized formulation. Efficacy was eligible on all tested species and in the case of staphylococcus aureus; the prepared semisolid formulation was even more effective.
机译:在药物制剂商业化之前,制药工业中最重要的问题之一是“预制剂”阶段。但是,在预配方研究中,已经非常重视对软件辅助统计设计的验证。这项研究的主要目的是报告基于统计混合物设计的半固体制剂分步预配制方法,并通过体外功效生物测定测试验证该软件所作的预测。极端顶点混合物设计(4个因子,4个水平)用于半固态聚维酮碘制剂的预配制,该制剂是使用不同的聚乙二醇凝胶的水可去除软膏。然后使用四个实际评估的响应值进行软件辅助(Minitab)分析,包括:可用碘,粘度(N指数和屈服值)和吸水能力。随后进行混合物分析,最后提出了优化配方。该制剂的功效通过体外微生物测试进行了生物测定,并计算了大肠杆菌,假单胞菌,金黄色葡萄球菌和白色念珠菌的MIC值,结果表明所测得的响应可接受。因此,可以得出结论,建议的设计具有足够的能力来预测实践中的响应。在为期一年的优化配方研究中,稳定性研究证明没有重大变化。在所有测试的物种和金黄色葡萄球菌的情况下,功效均合格;制备的半固体制剂甚至更有效。

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