泡沫辅助融合技术增强白藜芦醇溶解度的研究

M. Tawar, Kiran H. Raut, Reshma Chaudhary, N. Jain
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引用次数: 2

摘要

这项研究的基本原因是为了提高白藜芦醇的溶解度,从而最终提高溶出度,即药物的释放速度,从而增加药物的吸收。这里采用的方法是泡腾辅助融合技术。采用水溶性载体和碳酸氢钠制备了不同批次的样品。研究结果表明,与纯药物相比,该药物在磷酸盐缓冲液和蒸馏水等溶剂中的溶解度可提高10倍。配伍研究表明,药物与辅料之间无相互作用,微动力学性能表现出良好的流动性能和良好的可压缩性。制备的分散体产率在79.20±0.28% ~ 89.38±0.25%之间,释药率在10.87% ~ 99.14%之间。纯药在特定时间内的释药率小于70%,而优化批F5的释药率大于95%。XRD数据表明药物的晶体结构在制备过程中没有受到阻碍,SEM数据显示纯药物的表面形状为瓦片状,制备的分散体呈片状。从研究中可以得出结论,本研究中采用的方法可以证明是一种将药物的溶解度提高10倍的极好方法。
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Solubility Enhancement of Resveratrol by Effervescence Assisted Fusion Technique
The basic reason behind this study was to enhance the solubility rate of resveratrol which will finally enhance the dissolution i.e. the rate of drug release due to which the absorption of the drug will increase. The method applied here was effervescent assisted fusion technique. Various batches were prepared by employing water soluble carrier and sodium bicarbonate. The results obtained from the study revealed that the solubility of the drug can be increased up to 10 times than compared with the pure drug in various solvents i.e. phosphate buffer and distilled water. The compatibility study showed no interaction between drug and the excipient while the micromeretics property showed good flow property with good compressibility property. The percent yield of the dispersions prepared ranges between 79.20±0.28% - 89.38±0.25% while the drug release data showed a better rate of drug release than compared with the pure drug which ranges between 10.87% - 99.14%. The pure drug was having a drug release of less than 70% while the optimized batch F5 was having a drug release of more than 95% in the specific period of time. The XRD data showed that the drug’s crystalline structure was not hampered during the preparation while the SEM data revealed the surface shape of the pure drug which was tile shaped and the prepared dispersion was of flakes like formation. From the study it can be concluded that the methods employed in this study can be proven to be a excellent method for enhancing the solubility of the drug up to 10 folds.
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