Enhancement of Solubility and Dissolution Rate of BCS Class-II Fluvoxamine Tablets using Solvent Evaporation Solid Dispersion Technique

M. Srinivas, A. Singh
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引用次数: 4

Abstract

Aim: This research work was aimed to formulate Enhancing the solubility of Poorly soluble drug i.e. Fluvoxamine tablets by the solvent evaporation method, Fluvoxamine medicament is a selective serotonin reuptake inhibitor (SSRI) antidepressant agent. Purpose: The BCS class II drug Fluvoxamine consist low aqueous solubility and low oral bioavailability, for this reason to improve the biological performance of Fluvoxamine drug by solid dispersion mechanism. Methodolgy: The drug Fluvoxamine was formulated by using solvent evaporation technique, solid dispersions of Fluvoxamine were prepared with different carriers in different ratios of PEG 6000 & Mannitol (1:1, 1:2 and 1:3). Results: Results of prepared solid dispersions of Fluvoxamine by solid dispersion method Finally by comparing all the formulations, formulation (SF3) containing Fluvoxamine and PEG 6000 (1:3) shows better results. Original Research Article Srinivas and singh; JPRI, 33(31B): 44-53, 2021; Article no.JPRI.69597 45 Conclusion: Here we concluded that the poorly soluble drug solubility improving by solvent evaporation solid dispersion mechanism, and also developed six Fluvovamine formulations (FDF1FDF6) during this FDF4 shows maximum (98.9±0.8%) drug release at the end of time.
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溶剂蒸发-固体分散技术提高BCSⅡ类氟伏沙明片的溶解度和溶出度
目的:本研究旨在通过溶剂蒸发法制备提高难溶性药物氟伏沙明片溶解度的药物,氟伏沙胺是一种选择性5-羟色胺再摄取抑制剂(SSRI)抗抑郁剂。目的:BCSⅡ类药物氟伏沙明水溶性低,口服生物利用度低,因此通过固体分散机制提高氟伏沙胺的生物性能。方法:采用溶剂蒸发法制备氟伏沙明药物,用不同载体以不同比例的PEG 6000和甘露醇(1:1、1:2和1:3)制备氟伏沙明固体分散体。结果:用固体分散法制备氟伏沙明固体分散体的结果最后,通过对所有配方的比较,含有氟伏沙胺和PEG 6000(1:3)的配方(SF3)显示出更好的结果。原始研究文章Srinivas和singh;JPRI,33(31B):44-532021;文章编号:JPRI.69597 45结论:在这里,我们得出结论,通过溶剂蒸发-固体分散机制改善了难溶性药物的溶解度,并在此FDF4期间开发了六种Fluvovamine制剂(FDF1FDF6),在时间结束时显示出最大(98.9±0.8%)的药物释放。
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