首页> 外文期刊>International Journal of Pharmaceutical Sciences Review and Research >Design and in-vitro Evaluation of Floating Microspheres Containing Lactulose Using Emulsion Solvent Evaporation Technique
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Design and in-vitro Evaluation of Floating Microspheres Containing Lactulose Using Emulsion Solvent Evaporation Technique

机译:乳化溶剂蒸发技术对浮乳含乳糖微球的设计与体外评价

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摘要

The present investigation was concerned with formulation and evaluation of floating microspheres for Lactulose using Ethyl cellulose & HPMC as a release retarded material were prepared using emulsion solvent evaporation technique. Eleven different batches of microspheres were prepared by varying the concentration of drug polymer ratio from 1:0.5 to 1:5. The microspheres were characterized for drug content, percentage yield, particle size analysis and surface morphology. The results of all the physiochemical tests of all formulations were found to be favorable. In-vitro floatability studies reveled that most of the microspheres (64 - 94%) were floatable. The in-vitro % drug release was found to be in range of 89.18 to 97.89 %. At the end of 14 hrs. Formulation F showed best appropriate balance between buoyancy and drug release rate. Optimized formulation F was evaluated for FTIR, DSC and SEM. DSC and FTIR studies showed that the nature of pure drug Lactulose remains unaffected till the completion of process of microspheres formation. SEM photographs showed that the Floating microspheres were spherical in nature with smooth surface and uniform distribution of the drug within the microsphere.
机译:本研究涉及使用乙基纤维素和HPMC作为乳胶溶剂蒸发技术制备的缓释材料,对乳果糖浮微球的配制和评价。通过将药物聚合物比例的浓度从1:0.5更改为1:5,制备了十一批不同的微球。对微球的药物含量,百分产率,粒度分析和表面形态进行了表征。发现所有制剂的所有理化测试结果都是有利的。体外漂浮性研究表明,大多数微球(64-94%)是可漂浮的。发现体外%药物释放在89.18至97.89%的范围内。在14小时结束时。制剂F显示出浮力和药物释放速率之间的最佳适当平衡。评价了最佳配方F的FTIR,DSC和SEM。 DSC和FTIR研究表明,直到微球形成过程完成,纯药物乳果糖的性质仍不受影响。 SEM照片显示,漂浮微球本质上是球形的,具有光滑的表面和药物在微球内的均匀分布。

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