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Viscoelastic properties of Carbopol 940 gels and their relationships to piroxicam diffusion coefficients in gel bases.

机译:Carbopol 940凝胶的粘弹性质及其与吡罗昔康在凝胶基质中扩散系数的关系。

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PURPOSE: This study was conducted to determine the effect of formula compositions on viscoelastic properties of piroxicam gels using Carbopol 940 as a gelling agent and to determine the relationships between viscoelastic properties of Carbopol 940 gel bases and diffusion coefficients of piroxicam in gel bases. METHODS: Piroxicam gels (1.0% w/w) were prepared by using Carbopol 940 as a gelling agent and varying Carbopol 940 concentrations, glycerin, and sodium chloride contents. The in vitro release of piroxicam from gel bases to the receiving media, isotonic phosphate buffer solution (pH 7.4), were carried out using Franz-modified cell. The piroxicam diffusion coefficients were obtained by Higuchi's equation. Rheological property measurements of gel samples were performed via a cone and plate fluid rheometer. Relationships between viscoelastic properties of gel samples and piroxicam diffusion in gel bases were analyzed by Pearson's test at a p value of less than 0.05. RESULTS: All piroxicam gels exhibited predominantly elastic solid behavior whose magnitude depended on Carbopol 940 concentration. Preparations containing good solvent exhibited more elastic solid characters. In contrast, the piroxicam gels containing higher sodium chloride contents possessed more viscous fluid behavior. Analyzed by Pearson's test at a p value of less than 0.05, piroxicam diffusion coefficients were directly proportional to loss tangent, but were inversely proportional to storage modulus, loss modulus, complex modulus, and viscosity. CONCLUSIONS: There is a potential for predicting drug diffusion coefficients from their correlations to rheological parameters. This could be beneficial to the formulation design of transdermal drug delivery systems including mucoadhesive drug delivery systems.
机译:目的:进行这项研究来确定配方组合物对使用Carbopol 940作为胶凝剂的吡罗昔康凝胶的粘弹性的影响,并确定Carbopol 940凝胶基质的粘弹性与吡罗昔康在凝胶基质中的扩散系数之间的关系。方法:使用Carbopol 940作为胶凝剂并改变Carbopol 940的浓度,甘油和氯化钠含量,制备吡罗昔康凝胶(1.0%w / w)。使用Franz修饰的细胞将吡罗昔康从凝胶基质向等渗磷酸盐缓冲溶液(pH 7.4)的体外释放。吡罗昔康的扩散系数通过Higuchi方程获得。凝胶样品的流变性能测量是通过锥板流体流变仪进行的。凝胶样品的粘弹性质与吡罗昔康在凝胶基质中的扩散之间的关系通过Pearson检验分析,p值小于0.05。结果:所有吡罗昔康凝胶均表现出主要的弹性固体行为,其大小取决于Carbopol 940的浓度。含有良好溶剂的制剂表现出更多的弹性固体特性。相反,含有较高氯化钠含量的吡罗昔康凝胶具有更粘的流体行为。通过Pearson检验在p值小于0.05时分析,吡罗昔康的扩散系数与损耗角正切成正比,而与储能模量,损耗模量,复数模量和粘度成反比。结论:有可能根据其与流变学参数的相关性来预测药物扩散系数。这对于包括粘膜粘附药物递送系统的透皮药物递送系统的制剂设计可能是有益的。

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