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配方组成对滚压法制得的控释片性质的影响。

Effect of formulation composition on the properties of controlled release tablets prepared by roller compaction.

作者信息

Hariharan Madhusudan, Wowchuk Christina, Nkansah Paul, Gupta Vishal K

机构信息

Pfizer Global R&D, Pharmaceutical Sciences, Skokie, Illinois, USA.

出版信息

Drug Dev Ind Pharm. 2004 Jul;30(6):565-72. doi: 10.1081/ddc-120037487.

Abstract

This study discusses the effect of formulation composition on the physical characteristics and drug release behavior of controlled-release formulations made by roller compaction. The authors used mixture experimental design to study the effect of formulation components using diclofenac sodium as the model drug substance and varying relative amounts of microcrystalline cellulose (Avicel), hydroxypropyl methylcellulose (HPMC), and glyceryl behenate (Compritol). Dissolution studies revealed very little variability in drug release. The t70 values for the 13 formulations were found to vary between 260 and 550 min. A reduced cubic model was found to best fit the t70 data and gave an adjusted r-square of 0.9406. Each of the linear terms, the interaction terms between Compritol and Avicel and between all three of the tested factors were found to be significant. The longest release times were observed for formulations having higher concentrations of HPMC or Compritol. Tablets with higher concentrations of Avicel showed reduced ability to retard the release of the drug from the tablet matrix. Crushing strength showed systematic dependence on the formulation factors and could be modeled using a reduced quadratic model. The crushing strength values were highest at high concentrations of Avicel, while tablets with a high level of Compritol showed the lowest values. A predicted optimum formulation was derived by a numerical, multiresponse optimization technique. The validity of the model for predicting physical attributes of the product was also verified by experiment. The observed responses from the calculated optimum formulation were in very close agreement with values predicted by the model. The utility of a mixture experimental design for selecting formulation components of a roller compacted product was demonstrated. These simple statistical tools can allow a formulator to rationally select levels of various components in a formulation, improve the quality of products, and develop more robust processes.

摘要

本研究探讨了配方组成对滚压法制得的控释制剂物理特性及药物释放行为的影响。作者采用混合实验设计,以双氯芬酸钠为模型药物,微晶纤维素(微晶纤维素)、羟丙基甲基纤维素(羟丙甲纤维素)和山嵛酸甘油酯(Compritol)的相对用量不同,研究配方成分的影响。溶出度研究表明药物释放的变异性很小。13种制剂的t70值在260至550分钟之间变化。发现简化立方模型最适合t70数据,调整后的决定系数为0.9406。发现每个线性项、Compritol与微晶纤维素之间以及所有三个测试因素之间的相互作用项均具有显著性。观察到羟丙甲纤维素或Compritol浓度较高的制剂释放时间最长。微晶纤维素浓度较高的片剂延缓药物从片剂基质中释放的能力降低。抗压强度表现出对配方因素的系统性依赖,可以用简化二次模型进行建模。微晶纤维素高浓度时抗压强度值最高,而Compritol含量高的片剂抗压强度值最低。通过数值多响应优化技术得出了预测的最佳配方。还通过实验验证了该模型预测产品物理属性的有效性。计算得到的最佳配方的观察响应与模型预测值非常接近。证明了混合实验设计在选择滚压产品配方成分方面的实用性。这些简单的统计工具可以使配方设计师合理选择配方中各种成分的用量,提高产品质量,并开发更稳健的工艺。

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